ID: 127276557 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:242892812-242893459 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241950661..241951308) | | |
ID: 127276556 | H3K4me1 hESC enhancer GRCh37_chr2:242892163-242892811 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241950012..241950660) | | |
ID: 127276555 | H3K4me1 hESC enhancer GRCh37_chr2:242884151-242884650 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241942000..241942499) | | |
ID: 127276554 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:242843375-242844020 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241901224..241901869) | | |
ID: 127276553 | H3K4me1 hESC enhancer GRCh37_chr2:242842731-242843374 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241900580..241901223) | | |
ID: 127276552 | H3K4me1 hESC enhancer GRCh37_chr2:242842086-242842730 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241899935..241900579) | | |
ID: 127276551 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:242822944-242823534 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241880793..241881383) | | |
ID: 127276550 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:242813965-242814521 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241871813..241872369) | | |
ID: 127276549 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:242807941-242808722 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241865789..241866570) | | |
ID: 127276548 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:242800252-242801214 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241858100..241859062) | | |
ID: 127276547 | H3K4me1 hESC enhancer GRCh37_chr2:242776389-242776889 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241834212..241834712) | | |
ID: 124905350 | uncharacterized LOC124905350 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241844167..241846480) | | |
ID: 124905349 | uncharacterized LOC124905349 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241808315..241810696, complement) | | |
ID: 122889015 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:242784841-242785538 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241842689..241843386) | | |
ID: 110599582 | CEB1 minisatellite repeat instability region [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241803954..241809030) | | |
ID: 105373978 | uncharacterized LOC105373978 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241879034..241881327, complement) | | |
ID: 105373977 | uncharacterized LOC105373977 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241852980..241856276) | | |
ID: 101927289 | long intergenic non-protein coding RNA 1237 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241881363..242078722) | | |
ID: 285095 | family with sequence similarity 240 member C [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241893988..241902585, complement) | | |
ID: 285093 | receptor transporter protein 5 (putative) [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241869729..241873823) | C2orf85, CXXC11, Z3CXXC5 | |