ID: 132090594 | Neanderthal introgressed variant-containing enhancer experimental_60863 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63347910..63348079) | | |
ID: 127894241 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62036487-62037438 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63405134..63406085) | | |
ID: 127894240 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62025225-62025986 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63393872..63394633) | | |
ID: 127894239 | H3K4me1 hESC enhancer GRCh37_chr20:62013199-62013883 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63381847..63382531) | | |
ID: 127894238 | H3K4me1 hESC enhancer GRCh37_chr20:62006107-62006606 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63374755..63375254) | | |
ID: 127894237 | H3K4me1 hESC enhancer GRCh37_chr20:61992809-61993442 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63361457..63362090) | | |
ID: 127894236 | H3K4me1 hESC enhancer GRCh37_chr20:61952290-61952790 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63320938..63321438) | | |
ID: 127894235 | H3K4me1 hESC enhancer GRCh37_chr20:61924933-61925432 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63293581..63294080) | | |
ID: 127894234 | H3K4me1 hESC enhancer GRCh37_chr20:61924431-61924932 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63293079..63293580) | | |
ID: 126863087 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr20:61986832-61988031 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63355480..63356679) | | |
ID: 126863086 | BRD4-independent group 4 enhancer GRCh37_chr20:61971654-61972853 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63340302..63341501) | | |
ID: 125387319 | Sharpr-MPRA regulatory region 327 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63409896..63410190) | | |
ID: 125387318 | Sharpr-MPRA regulatory region 785 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63377657..63377951) | | |
ID: 124904953 | uncharacterized LOC124904953 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63376315..63381890, complement) | | |
ID: 121627914 | Sharpr-MPRA regulatory region 8221 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63377377..63377671) | | |
ID: 106480006 | RNA, U6 small nuclear 994, pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63337355..63337424) | | |
ID: 105372724 | uncharacterized LOC105372724 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63411265..63413350) | | |
ID: 100130587 | uncharacterized LOC100130587 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63359988..63371177) | | |
ID: 57642 | collagen type XX alpha 1 chain [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63293186..63334806) | | 619390 |
ID: 3785 | potassium voltage-gated channel subfamily Q member 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63400208..63472655, complement) | BFNC, DEE7, EBN, EBN1, ENB1, HNSPC, KCNA11, KV7.2 | 602235 |