ID: 132090281 | Neanderthal introgressed variant-containing enhancer experimental_37742 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80763778..80763947) | | |
ID: 132090280 | Neanderthal introgressed variant-containing enhancer experimental_37671 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80638517..80638686) | | |
ID: 132090279 | Neanderthal introgressed variant-containing enhancer experimental_37660 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80605370..80605539) | | |
ID: 130056207 | ATAC-STARR-seq lymphoblastoid active region 8824 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81170411..81170780) | | |
ID: 130056206 | ATAC-STARR-seq lymphoblastoid active region 8823 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81170131..81170190) | | |
ID: 130056205 | ATAC-STARR-seq lymphoblastoid silent region 5983 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80996532..80996591) | | |
ID: 130056204 | ATAC-STARR-seq lymphoblastoid active region 8822 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80941953..80942032) | | |
ID: 130056203 | ATAC-STARR-seq lymphoblastoid active region 8821 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80941573..80941652) | | |
ID: 130056202 | ATAC-STARR-seq lymphoblastoid active region 8820 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80931938..80931987) | | |
ID: 130056201 | ATAC-STARR-seq lymphoblastoid active region 8819 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80931058..80931127) | | |
ID: 130056200 | ATAC-STARR-seq lymphoblastoid active region 8818 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80930908..80931037) | | |
ID: 129663471 | ReSE screen-validated silencer GRCh37_chr14:81507651-81507772 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81041307..81041428) | | |
ID: 127828136 | H3K4me1 hESC enhancer GRCh37_chr14:81439665-81440164 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80973321..80973820) | | |
ID: 127828135 | H3K4me1 hESC enhancer GRCh37_chr14:81439163-81439664 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80972819..80973320) | | |
ID: 127828134 | OCT4-NANOG hESC enhancer GRCh37_chr14:80930624-80931315 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80464281..80464972) | | |
ID: 105370594 | uncharacterized LOC105370594 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81168772..81171835) | | |
ID: 101928462 | uncharacterized LOC101928462 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81014066..81170406, complement) | | |
ID: 100628307 | DIO2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80211419..80455467) | | |
ID: 100431177 | GPRASP3 pseudogene 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80981593..80985795) | BHLHB9P1 | |
ID: 677845 | small nucleolar RNA, H/ACA box 79 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81202695..81202834, complement) | ACA65A, SNORA79 | |