ID: 130060993 | ATAC-STARR-seq lymphoblastoid silent region 8602 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44829600..44829889) | | |
ID: 130060992 | ATAC-STARR-seq lymphoblastoid silent region 8601 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44779468..44779607) | | |
ID: 127887029 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:42908287-42909260 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44830919..44831892) | | |
ID: 127887028 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr17:42907313-42908286 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44829945..44830918) | | |
ID: 127887027 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:42856011-42856852 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44778643..44779484) | | |
ID: 127887026 | H3K4me1 hESC enhancer GRCh37_chr17:42853416-42853916 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44775891..44776548) | | |
ID: 127887025 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:42835997-42836548 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44758629..44759180) | | |
ID: 127887024 | H3K4me1 hESC enhancer GRCh37_chr17:42830428-42830928 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44753060..44753560) | | |
ID: 107985044 | uncharacterized LOC107985044 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44734093..44740907, complement) | | |
ID: 100271035 | ribosomal protein L6 pseudogene 26 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44719737..44720615, complement) | RPL6_9_1550 | |
ID: 80174 | DBF4B-CDC7 kinase regulatory subunit [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44708665..44752264) | ASKL1, CHIFB, DRF1, ZDBF1B | 611661 |
ID: 51751 | HIG1 hypoxia inducible domain family member 1B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44844860..44850476) | CLST11240, CLST11240-15 | 620420 |
ID: 10052 | gap junction protein gamma 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44794104..44831364, complement) | CX45, GJA7 | 608655 |
ID: 9343 | elongation factor Tu GTP binding domain containing 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44849948..44899445, complement) | MFDGA, MFDM, SNRNP116, Snrp116, Snu114, U5-116KD | 603892 |
ID: 4185 | ADAM metallopeptidase domain 11 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44758988..44781846) | MDC | 155120 |