ID: 132090437 | Neanderthal introgressed variant-containing enhancer experimental_46330 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (796546..796715) | | |
ID: 130058140 | ATAC-STARR-seq lymphoblastoid silent region 6961 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (813722..813801) | | |
ID: 130058139 | ATAC-STARR-seq lymphoblastoid active region 10215 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (807838..808067) | | |
ID: 130058138 | ATAC-STARR-seq lymphoblastoid silent region 6960 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (807548..807757) | | |
ID: 130058137 | ATAC-STARR-seq lymphoblastoid silent region 6959 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (788854..788913) | | |
ID: 130058136 | ATAC-STARR-seq lymphoblastoid silent region 6958 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (788214..788673) | | |
ID: 130058135 | ATAC-STARR-seq lymphoblastoid silent region 6957 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (788104..788193) | | |
ID: 129663715 | ReSE screen-validated silencer GRCh37_chr16:946091-946310 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (896091..896310) | | |
ID: 127882685 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:979379-979960 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (929379..929960) | | |
ID: 127882684 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:978795-979378 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (928795..929378) | | |
ID: 127882683 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:966023-966972 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (916023..916972) | | |
ID: 127882682 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:952075-952792 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (902075..902792) | | |
ID: 127882681 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:951356-952074 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (901356..902074) | | |
ID: 127882680 | H3K4me1 hESC enhancer GRCh37_chr16:940581-941424 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (890581..891424) | | |
ID: 127882679 | H3K4me1 hESC enhancer GRCh37_chr16:936416-936993 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (886416..886993) | | |
ID: 127882678 | H3K4me1 hESC enhancer GRCh37_chr16:935837-936415 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (885837..886415) | | |
ID: 127882677 | H3K4me1 hESC enhancer GRCh37_chr16:890022-890522 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (840022..840522) | | |
ID: 127882676 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:867140-867640 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (817140..817640) | | |
ID: 127882675 | H3K4me1 hESC enhancer GRCh37_chr16:853979-854522 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (803979..804522) | | |
ID: 127882674 | H3K4me1 hESC enhancer GRCh37_chr16:852890-853434 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (802890..803434) | | |