ID: 127828320 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:93175352-93175977 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92709007..92709632) | | |
ID: 127828319 | H3K4me1 hESC enhancer GRCh37_chr14:93152626-93153253 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92686281..92686908) | | |
ID: 127828318 | H3K4me1 hESC enhancer GRCh37_chr14:93128149-93128650 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92661804..92662305) | | |
ID: 127828317 | H3K4me1 hESC enhancer GRCh37_chr14:93122369-93122870 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92656024..92656525) | | |
ID: 127828316 | NANOG hESC enhancer GRCh37_chr14:93039726-93040227 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92573381..92573882) | | |
ID: 127828315 | H3K4me1 hESC enhancer GRCh37_chr14:92997985-92998485 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92531641..92532141) | | |
ID: 127828314 | H3K4me1 hESC enhancer GRCh37_chr14:92997484-92997984 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92531140..92531640) | | |
ID: 127828313 | H3K4me1 hESC enhancer GRCh37_chr14:92994802-92995558 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92528458..92529214) | | |
ID: 127828312 | H3K4me1 hESC enhancer GRCh37_chr14:92994044-92994801 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92527700..92528457) | | |
ID: 127828311 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:92990985-92991808 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92524641..92525464) | | |
ID: 127828310 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:92980671-92981174 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92514325..92514830) | | |
ID: 127828309 | H3K4me1 hESC enhancer GRCh37_chr14:92967105-92967604 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92500761..92501260) | | |
ID: 127828308 | H3K4me1 hESC enhancer GRCh37_chr14:92966603-92967104 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92500259..92500760) | | |
ID: 126862026 | MED14-independent group 3 enhancer GRCh37_chr14:93090702-93091901 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92624357..92625556) | | |
ID: 125078026 | Sharpr-MPRA regulatory region 11533 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92690524..92690818) | | |
ID: 125078025 | Sharpr-MPRA regulatory region 13986 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92687864..92688158) | | |
ID: 125078024 | Sharpr-MPRA regulatory region 14383 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92611004..92611298) | | |
ID: 124903365 | uncharacterized LOC124903365 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92514374..92515511) | | |
ID: 124903364 | uncharacterized LOC124903364 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92669111..92673107, complement) | | |
ID: 123041 | solute carrier family 24 member 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92322581..92501481) | AI2A5, NCKX4, SHEP6, SLC24A2 | 609840 |