ID: 130066700 | ATAC-STARR-seq lymphoblastoid active region 18479 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41432340..41432419) | | |
ID: 130066699 | ATAC-STARR-seq lymphoblastoid active region 18478 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41432270..41432329) | | |
ID: 130066698 | ATAC-STARR-seq lymphoblastoid active region 18477 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41425906..41426345) | | |
ID: 130066697 | ATAC-STARR-seq lymphoblastoid silent region 13332 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41420244..41420523) | | |
ID: 130066696 | ATAC-STARR-seq lymphoblastoid active region 18474 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41368355..41368404) | | |
ID: 130066695 | ATAC-STARR-seq lymphoblastoid active region 18473 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41367535..41367634) | | |
ID: 130066694 | ATAC-STARR-seq lymphoblastoid silent region 13330 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41364561..41364610) | | |
ID: 130066693 | ATAC-STARR-seq lymphoblastoid active region 18472 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41361732..41362571) | | |
ID: 130066692 | ATAC-STARR-seq lymphoblastoid active region 18471 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41361452..41361711) | | |
ID: 130066691 | ATAC-STARR-seq lymphoblastoid active region 18470 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41358245..41358544) | | |
ID: 130066690 | ATAC-STARR-seq lymphoblastoid silent region 13329 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41167719..41168168) | | |
ID: 129664735 | ReSE screen-validated silencer GRCh37_chr21:42612073-42612217 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41240146..41240290) | | |
ID: 128849172 | melanoma risk locus-associated MPRA allelic enhancers 21:42746568 and 21:42746578 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41374569..41374731) | | |
ID: 128772427 | melanoma risk locus-associated MPRA allelic enhancer 21:42745414 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41373415..41373559) | | |
ID: 127894716 | H3K4me1 hESC enhancer GRCh37_chr21:42830117-42830618 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41458190..41458691) | | |
ID: 127894715 | H3K4me1 hESC enhancer GRCh37_chr21:42750999-42751498 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41379072..41379571) | | |
ID: 127894714 | H3K4me1 hESC enhancer GRCh37_chr21:42750497-42750998 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41378570..41379071) | | |
ID: 127894713 | H3K4me1 hESC enhancer GRCh37_chr21:42741403-42742089 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41369476..41370324) | | |
ID: 127894712 | H3K4me1 hESC enhancer GRCh37_chr21:42740714-42741402 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41368787..41369475) | | |
ID: 127894711 | H3K4me1 hESC enhancer GRCh37_chr21:42739613-42740114 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41367686..41368187) | | |