ID: 132088749 | Neanderthal introgressed variant-containing enhancer experimental_978 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166150052..166150221) | | |
ID: 132088748 | Neanderthal introgressed variant-containing enhancer experimental_966 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166137942..166138111) | | |
ID: 132088744 | Neanderthal introgressed variant-containing enhancer experimental_946 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166116419..166116588) | | |
ID: 132088596 | Neanderthal introgressed variant-containing enhancer experimental_1002 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166176291..166176460) | | |
ID: 129931824 | ATAC-STARR-seq lymphoblastoid silent region 1510 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166182448..166182577) | | |
ID: 129931823 | ATAC-STARR-seq lymphoblastoid active region 2025 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166170176..166170255) | | |
ID: 129931822 | ATAC-STARR-seq lymphoblastoid silent region 1509 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166169276..166169335) | | |
ID: 129931821 | ATAC-STARR-seq lymphoblastoid silent region 1508 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166166752..166167241) | | |
ID: 129388619 | MPRA-validated peak439 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166069499..166069699) | | |
ID: 127270744 | H3K4me1 hESC enhancer GRCh37_chr1:166135105-166136007 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166165868..166166770) | | |
ID: 127270743 | OCT4-NANOG hESC enhancer GRCh37_chr1:166097641-166098142 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166128404..166128905) | | |
ID: 127270742 | H3K27ac hESC enhancer GRCh37_chr1:166033205-166033704 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166063968..166064467) | | |
ID: 126805901 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:166009027-166010226 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166039790..166040989) | | |
ID: 112268276 | uncharacterized LOC112268276 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166165877..166340900) | | |
ID: 105371586 | FAM78B antisense RNA 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166080736..166091567) | | |
ID: 100873299 | RNA, 5S ribosomal pseudogene 64 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166042244..166042350) | RN5S64 | |
ID: 100126349 | microRNA 921 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166154743..166154798, complement) | MIRN921, hsa-mir-921 | |
ID: 401975 | RPS3A pseudogene 10 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166022190..166023075) | RPS3A_2_114 | |
ID: 284685 | EWS RNA binding protein 1 pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166275454..166277636, complement) | | |
ID: 149297 | family with sequence similarity 78 member B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (166055918..166167001, complement) | | |