| ID: 129660038 | ReSE screen-validated silencer GRCh37_chrX:1727169-1727341 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1608276..1608448); Chromosome Y, NC_000024.10 (1608276..1608448) | | |
| ID: 129660037 | ReSE screen-validated silencer GRCh37_chrX:1599821-1599989 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1480928..1481096); Chromosome Y, NC_000024.10 (1480928..1481096) | | |
| ID: 127138854 | H3K4me1 hESC enhancer GRCh37_chrY:1778143-1778642 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1709250..1709749); Chromosome Y, NC_000024.10 (1709250..1709749) | | |
| ID: 127138853 | OCT4-NANOG hESC enhancer GRCh37_chrY:1747612-1748179 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1678719..1679286); Chromosome Y, NC_000024.10 (1678719..1679286) | | |
| ID: 127138838 | H3K4me1 hESC enhancer GRCh37_chrX:1883833-1884333 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1764940..1765440); Chromosome Y, NC_000024.10 (1764940..1765440) | | |
| ID: 127138837 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrY:1718443-1718962 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1649550..1650069); Chromosome Y, NC_000024.10 (1649550..1650069) | | |
| ID: 127138836 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrY:1678943-1679525 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1610050..1610632); Chromosome Y, NC_000024.10 (1610050..1610632) | | |
| ID: 127138835 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrY:1678358-1678942 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1609465..1610049); Chromosome Y, NC_000024.10 (1609465..1610049) | | |
| ID: 127138834 | H3K4me1 hESC enhancer GRCh37_chrX:1776693-1777192 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1657800..1658299); Chromosome Y, NC_000024.10 (1657800..1658299) | | |
| ID: 127138833 | H3K4me1 hESC enhancer GRCh37_chrX:1776191-1776692 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1657298..1657799); Chromosome Y, NC_000024.10 (1657298..1657799) | | |
| ID: 127138832 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chrX:1737403-1738040 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1618510..1619147); Chromosome Y, NC_000024.10 (1618510..1619147) | | |
| ID: 127138831 | hESC enhancers GRCh37_chrX:1600455-1601166 and GRCh37_chrY:1550663-1551162 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1481562..1482273); Chromosome Y, NC_000024.10 (1481562..1482273) | | |
| ID: 127138830 | H3K4me1 hESC enhancer GRCh37_chrX:1585389-1585889 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1466496..1466996); Chromosome Y, NC_000024.10 (1466496..1466996) | | |
| ID: 124908777 | uncharacterized LOC124908777 [Homo sapiens (human)] | | | |
| ID: 105379413 | uncharacterized LOC105379413 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1771053..1784602); Chromosome Y, NC_000024.10 (1771053..1784602) | | |
| ID: 105373105 | long intergenic non-protein coding RNA 2968 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1732419..1755984); Chromosome Y, NC_000024.10 (1732419..1755984) | | |
| ID: 286530 | P2Y receptor family member 8 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1462581..1537185, complement); Chromosome Y, NC_000024.10 (1462581..1537185, complement) | P2Y8 | 300525 |
| ID: 80161 | ASMTL antisense RNA 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1400531..1415421); Chromosome Y, NC_000024.10 (1400531..1415421) | ASMTL-AS, ASMTLAS, CXYorf2, NCRNA00105 | |
| ID: 8623 | acetylserotonin O-methyltransferase like [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1403139..1453756, complement); Chromosome Y, NC_000024.10 (1403139..1453756, complement) | ASMTLXY, ASTML, ASMTL | 300162, 400011 |
| ID: 8227 | A-kinase anchoring protein 17A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1591604..1602520); Chromosome Y, NC_000024.10 (1591604..1602520) | 721P, AKAP-17A, CCDC133, CXYorf3, DXYS155E, PRKA17A, SFRS17A, XE7, XE7Y | 312095, 465000 |