ID: 132090662 | Neanderthal introgressed variant-containing enhancer experimental_7558 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36591346..36591515) | | |
ID: 129930144 | ATAC-STARR-seq lymphoblastoid active region 760 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36665738..36665787) | | |
ID: 129930143 | ATAC-STARR-seq lymphoblastoid active region 759 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36554080..36554129) | | |
ID: 129930142 | ATAC-STARR-seq lymphoblastoid active region 758 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36553740..36553939) | | |
ID: 129930141 | ATAC-STARR-seq lymphoblastoid active region 757 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36516717..36516766) | | |
ID: 129930140 | ATAC-STARR-seq lymphoblastoid active region 756 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36516587..36516676) | | |
ID: 127268725 | H3K4me1 hESC enhancer GRCh37_chr1:37054575-37055075 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36588974..36589474) | | |
ID: 127268724 | H3K27ac hESC enhancer GRCh37_chr1:37000487-37000987 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36534886..36535386) | | |
ID: 127268723 | H3K27ac hESC enhancer GRCh37_chr1:36999986-37000486 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36534385..36534885) | | |
ID: 127268722 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr1:36989709-36990209 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36524108..36524608) | | |
ID: 127268721 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr1:36989208-36989708 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36523607..36524107) | | |
ID: 127268720 | H3K4me1 hESC enhancer GRCh37_chr1:36946417-36947202 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36480816..36481601) | | |
ID: 127268719 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:36931829-36932691 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36466228..36467090) | | |
ID: 126805699 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:36929292-36930491 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36463392..36465197) | | |
ID: 122056840 | Sharpr-MPRA regulatory region 1123 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36572208..36572502) | | |
ID: 122056839 | Sharpr-MPRA regulatory region 4345 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36492628..36492922) | | |
ID: 107984941 | uncharacterized LOC107984941 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36676241..36702321, complement) | | |
ID: 105378648 | uncharacterized LOC105378648 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36686708..36694967, complement) | | |
ID: 100462786 | ferritin light chain pseudogene 18 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36630335..36630812) | | |
ID: 64960 | mitochondrial ribosomal protein S15 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36455718..36464384, complement) | DC37, MPR-S15, RPMS15, S15mt, uS15m | 611979 |