ID: 127827642 | OCT4-NANOG hESC enhancer GRCh37_chr14:57369890-57370816 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56903172..56904098) | | |
ID: 127827641 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr14:57361673-57362238 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56894955..56895520) | | |
ID: 127827640 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:57313709-57314674 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56846991..56847956) | | |
ID: 127827639 | H3K4me1 hESC enhancer GRCh37_chr14:57278577-57279469 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56811859..56812751) | | |
ID: 127827638 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:57272200-57273038 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56805482..56806320) | | |
ID: 127827637 | H3K4me1 hESC enhancer GRCh37_chr14:57270522-57271360 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56803804..56804642) | | |
ID: 124903323 | uncharacterized LOC124903323 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56953824..57017684, complement) | | |
ID: 110121404 | VISTA enhancer hs1579 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56853946..56857601) | | |
ID: 110121333 | VISTA enhancer hs1218 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56964169..56965628) | | |
ID: 110121324 | VISTA enhancer hs1150 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56952290..56954727) | | |
ID: 106481844 | RNA, 7SL, cytoplasmic 461, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56824375..56824656, complement) | | |
ID: 106481560 | RNA, U6 small nuclear 1204, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56824986..56825092) | | |
ID: 100309464 | OTX2 antisense RNA 1 (head to head) [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56812006..56931308) | OTX2OS1 | |
ID: 5015 | orthodenticle homeobox 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (56799905..56810479, complement) | CPHD6, MCOPS5 | 600037 |