ID: 132090652 | Neanderthal introgressed variant-containing enhancer experimental_63425 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43137439..43137608) | | |
ID: 130067632 | ATAC-STARR-seq lymphoblastoid active region 19186 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43152152..43152251) | | |
ID: 130067631 | ATAC-STARR-seq lymphoblastoid silent region 13856 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43151311..43151530) | | |
ID: 130067630 | ATAC-STARR-seq lymphoblastoid active region 19185 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43147892..43148101) | | |
ID: 130067629 | ATAC-STARR-seq lymphoblastoid silent region 13855 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43143153..43143422) | | |
ID: 130067628 | ATAC-STARR-seq lymphoblastoid active region 19183 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43119237..43119396) | | |
ID: 130067627 | ATAC-STARR-seq lymphoblastoid silent region 13854 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43111400..43111619) | | |
ID: 130067626 | ATAC-STARR-seq lymphoblastoid silent region 13852 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43090306..43090365) | | |
ID: 127896527 | H3K4me1 hESC enhancer GRCh37_chr22:43559052-43559555 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43163046..43163549) | | |
ID: 127896526 | H3K4me1 hESC enhancer GRCh37_chr22:43553089-43553609 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43157083..43157603) | | |
ID: 127896525 | H3K4me1 hESC enhancer GRCh37_chr22:43524576-43525453 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43128570..43129447) | | |
ID: 127896524 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:43506823-43507381 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43110700..43111375) | | |
ID: 127896523 | H3K4me1 hESC enhancer GRCh37_chr22:43475054-43475575 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43079048..43079569) | | |
ID: 127896522 | H3K4me1 hESC enhancer GRCh37_chr22:43474531-43475053 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43078525..43079047) | | |
ID: 121853045 | Sharpr-MPRA regulatory region 7153 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43101263..43101557) | | |
ID: 121627948 | Sharpr-MPRA regulatory region 1995 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43089159..43089557) | | |
ID: 100506679 | TTLL1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43038585..43052366) | | |
ID: 100271372 | ribosomal protein S25 pseudogene 10 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43092134..43092579) | RPS25_3_1755 | |
ID: 27349 | malonyl-CoA-acyl carrier protein transacylase [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43132206..43143398, complement) | FASN2C, MCT, MCT1, MT, NET62, OPA15, fabD | 614479 |
ID: 25809 | TTL family tubulin polyglutamylase complex subunit L1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43039516..43089391, complement) | C22orf7, HS323M22B, TPGS3 | 608955 |