ID: 127274888 | H3K4me1 hESC enhancer GRCh37_chr2:135218313-135218812 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134460742..134461241) | | |
ID: 127274887 | H3K4me1 hESC enhancer GRCh37_chr2:135217811-135218312 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134460240..134460741) | | |
ID: 127274886 | H3K4me1 hESC enhancer GRCh37_chr2:135201292-135201792 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134443721..134444221) | | |
ID: 127274885 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:135129934-135130438 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134372363..134372867) | | |
ID: 127274884 | H3K4me1 hESC enhancer GRCh37_chr2:135002735-135003235 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134245164..134245664) | | |
ID: 127274883 | H3K4me1 hESC enhancer GRCh37_chr2:135002234-135002734 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134244663..134245163) | | |
ID: 127274882 | NANOG hESC enhancer GRCh37_chr2:134960700-134961201 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134203129..134203630) | | |
ID: 127274881 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:134916038-134916642 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134158467..134159071) | | |
ID: 127274880 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:134915432-134916037 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134157861..134158466) | | |
ID: 127274879 | OCT4-NANOG hESC enhancer GRCh37_chr2:134891786-134892407 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134134215..134134836) | | |
ID: 127274878 | NANOG hESC enhancer GRCh37_chr2:134891163-134891785 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134133592..134134214) | | |
ID: 127274877 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:134867203-134867862 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134109632..134110291) | | |
ID: 127274876 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:134866541-134867202 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134108970..134109631) | | |
ID: 122819157 | Sharpr-MPRA regulatory region 6492 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134432238..134432532) | | |
ID: 122819156 | Sharpr-MPRA regulatory region 5769 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134206618..134206912) | | |
ID: 100873375 | RNA, 5S ribosomal pseudogene 104 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134231195..134231312) | RN5S104 | |
ID: 100500878 | microRNA 3679 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134127125..134127192) | mir-3679 | |
ID: 266643 | epididymal protein 3C, pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134319554..134320180, complement) | FAM12CP, HE3-GAMMA | |
ID: 81615 | transmembrane protein 163 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134455759..134719000, complement) | DC29, HLD25, SLC30A11, SV31 | 618978 |
ID: 4249 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134119935..134454621) | GNT-V, GNT-VAA, glcNAc-T V, MGAT5 | 601774 |