ID: 130055281 | ATAC-STARR-seq lymphoblastoid silent region 5581 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21092574..21092783) | | |
ID: 130055280 | ATAC-STARR-seq lymphoblastoid silent region 5579 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21070467..21070536) | | |
ID: 130055279 | ATAC-STARR-seq lymphoblastoid silent region 5578 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21070237..21070456) | | |
ID: 130055278 | ATAC-STARR-seq lymphoblastoid silent region 5577 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21068602..21068701) | | |
ID: 127827197 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:21571456-21572200 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21103297..21104041) | | |
ID: 127827196 | H3K27ac hESC enhancer GRCh37_chr14:21566496-21566996 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21098337..21098837) | | |
ID: 127827195 | H3K27ac hESC enhancer GRCh37_chr14:21565235-21565736 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21097076..21097577) | | |
ID: 127827194 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:21559284-21560128 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21091125..21091969) | | |
ID: 127827193 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:21558438-21559283 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21090279..21091124) | | |
ID: 127827192 | H3K4me1 hESC enhancer GRCh37_chr14:21555489-21556031 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21087330..21087872) | | |
ID: 127827191 | H3K4me1 hESC enhancer GRCh37_chr14:21554944-21555488 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21086785..21087329) | | |
ID: 127827190 | H3K27ac hESC enhancer GRCh37_chr14:21539187-21539808 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21071028..21071649) | | |
ID: 126861886 | BRD4-independent group 4 enhancer GRCh37_chr14:21552808-21554007 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21084649..21085848) | | |
ID: 126861885 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:21550650-21551849 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21082491..21083690) | | |
ID: 124958012 | Sharpr-MPRA regulatory region 8150 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21092930..21093224) | | |
ID: 105370398 | uncharacterized LOC105370398 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21046397..21048695, complement) | | |
ID: 100420763 | cytoskeleton associated protein 2 pseudogene 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21110912..21113214, complement) | | |
ID: 643382 | transmembrane protein 253 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21098836..21103724) | C14orf176, C14orf95, NCRNA00220 | |
ID: 122665 | ribonuclease A family member 8 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21057822..21058455) | RAE2 | 612485 |
ID: 57447 | NDRG family member 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (21016763..21070872, complement) | SYLD | 605272 |