| ID: 132088711 | Neanderthal introgressed variant-containing enhancer experimental_7809 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37386255..37386424) | | |
| ID: 129930154 | ATAC-STARR-seq lymphoblastoid active region 769 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37484338..37484467) | | |
| ID: 129930153 | ATAC-STARR-seq lymphoblastoid active region 767 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37477235..37477534) | | |
| ID: 129930152 | ATAC-STARR-seq lymphoblastoid active region 766 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37475425..37475524) | | |
| ID: 129930151 | ATAC-STARR-seq lymphoblastoid silent region 671 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37474315..37474774) | | |
| ID: 129930150 | ATAC-STARR-seq lymphoblastoid silent region 670 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37473755..37473854) | | |
| ID: 129660217 | ReSE screen-validated silencer GRCh37_chr1:37827606-37827793 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37362005..37362192) | | |
| ID: 127268750 | H3K4me1 hESC enhancer GRCh37_chr1:37876731-37877231 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37411130..37411630) | | |
| ID: 127268749 | H3K4me1 hESC enhancer GRCh37_chr1:37876230-37876730 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37410629..37411129) | | |
| ID: 126805702 | MED14-independent group 3 enhancer GRCh37_chr1:37920349-37921548 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37454748..37455947) | | |
| ID: 126805701 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:37916959-37918158 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37451358..37452750) | | |
| ID: 112577589 | H3K4me1 hESC enhancers GRCh37_chr1:37944526-37945352 and GRCh37_chr1:37945353-37946179 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37478925..37480578) | | |
| ID: 107984942 | uncharacterized LOC107984942 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37351698..37373807, complement) | | |
| ID: 102465438 | microRNA 6732 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37480230..37480289) | hsa-mir-6732 | |
| ID: 100847010 | microRNA 5581 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37500935..37500994, complement) | | |
| ID: 100270903 | ribosomal protein S29 pseudogene 6 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37330852..37330979) | RPS29_1_32 | |
| ID: 728431 | lncRNA induced by TGF-beta and antagonizes TGF-beta signaling 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37454879..37474443, complement) | LINC01137, ZC3H12A-DT | |
| ID: 80149 | zinc finger CCCH-type containing 12A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37474580..37484377) | MCPIP, MCPIP-1, MCPIP1, Reg1, dJ423B22.1 | 610562 |
| ID: 64769 | MYST/Esa1 associated factor 6 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37489993..37514766, complement) | C1orf149, CENP-28, EAF6, NY-SAR-91 | 611001 |