ID: 127882477 | H3K4me1 hESC enhancer GRCh37_chr1:31907359-31908163 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31434512..31435316) | | |
ID: 126805682 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:31943609-31944808 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31470762..31471961) | | |
ID: 126805681 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:31926120-31927319 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31453273..31454472) | | |
ID: 124903900 | uncharacterized LOC124903900 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31426410..31471476, complement) | | |
ID: 110594336 | MS1 minisatellite repeat instability region [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31428806..31434663) | | |
ID: 105379772 | uncharacterized LOC105379772 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31471118..31482156) | | |
ID: 105378625 | uncharacterized LOC105378625 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31445854..31450649) | | |
ID: 441880 | eukaryotic translation elongation factor 1 alpha 1 pseudogene 46 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31487591..31488973, complement) | | |
ID: 347735 | serine incorporator 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31409777..31434678) | FKSG84, PRO0899, TDE2, TDE2L | 614549 |