ID: 130058421 | ATAC-STARR-seq lymphoblastoid silent region 7190 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10181636..10181695) | | |
ID: 130058420 | ATAC-STARR-seq lymphoblastoid silent region 7189 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10181516..10181625) | | |
ID: 130058419 | ATAC-STARR-seq lymphoblastoid silent region 7188 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10039615..10039664) | | |
ID: 130058418 | ATAC-STARR-seq lymphoblastoid active region 10376 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9843359..9843608) | | |
ID: 127883119 | H3K4me1 hESC enhancer GRCh37_chr16:10132543-10133043 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10038686..10039186) | | |
ID: 127883118 | NANOG hESC enhancer GRCh37_chr16:10050616-10051155 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9956759..9957298) | | |
ID: 127883117 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:9774851-9775778 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9680994..9681921) | | |
ID: 127883116 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:9773923-9774850 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9680066..9680993) | | |
ID: 127883115 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr16:9771199-9771764 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9677342..9677907) | | |
ID: 127883114 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:9770634-9771198 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9676777..9677341) | | |
ID: 127883113 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:9768371-9768936 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9674514..9675079) | | |
ID: 127883112 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:9767805-9768370 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9673948..9674513) | | |
ID: 127883111 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr16:9764099-9764878 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9670242..9671021) | | |
ID: 125146403 | Sharpr-MPRA regulatory region 8841 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10078592..10078886) | | |
ID: 107984900 | uncharacterized LOC107984900 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10214505..10217160, complement) | | |
ID: 105371077 | uncharacterized LOC105371077 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9790975..9810765) | | |
ID: 105371076 | uncharacterized LOC105371076 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10031636..10037297) | | |
ID: 100873656 | RNA, 5S ribosomal pseudogene 404 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9600097..9600228) | RN5S404 | |
ID: 727833 | inosine monophosphate dehydrogenase 1 pseudogene 11 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10111309..10113590) | IMPDH1, IMPDHL1 | |
ID: 2903 | glutamate ionotropic receptor NMDA type subunit 2A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9753404..10182908, complement) | EPND, FESD, GluN2A, LKS, NMDAR2A, NR2A | 138253 |