ID: 127405757 | H3K4me1 hESC enhancer GRCh37_chr6:31125321-31125821 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31157544..31158044) | | |
ID: 127405756 | H3K4me1 hESC enhancer GRCh37_chr6:31124820-31125320 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31157043..31157543) | | |
ID: 127405754 | H3K4me1 hESC enhancer GRCh37_chr6:31105363-31106343 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31137586..31138566) | | |
ID: 127405753 | H3K4me1 hESC enhancer GRCh37_chr6:31094370-31094969 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31126593..31127192) | | |
ID: 127405752 | H3K4me1 hESC enhancer GRCh37_chr6:31093769-31094369 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31125992..31126592) | | |
ID: 127405751 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31093168-31093768 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31125391..31125991) | | |
ID: 127405750 | H3K4me1 hESC enhancer GRCh37_chr6:31084517-31085386 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31116740..31117609) | | |
ID: 127405749 | H3K27ac hESC enhancer GRCh37_chr6:31051567-31052066 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31083790..31084289) | | |
ID: 106481537 | RNA, U6 small nuclear 1133, pseudogene [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31083040..31083103) | RNU6-186P | |
ID: 493825 | RNA polymerase II subunit L pseudogene 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31140727..31140913) | POLR2LP | |
ID: 170680 | psoriasis susceptibility 1 candidate 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31137534..31139066, complement) | C6orf17, SPR1 | 613526 |
ID: 170679 | psoriasis susceptibility 1 candidate 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31114800..31140092) | C6orf16, SEEK1 | 613525 |
ID: 54535 | coiled-coil alpha-helical rod protein 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31142439..31158197, complement) | C6orf18, HCR, SBP, pg8 | 605310 |
ID: 29113 | chromosome 6 open reading frame 15 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31111223..31112575, complement) | STG | 611401 |
ID: 1041 | corneodesmosin [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31115087..31120446, complement) | HTSS, HTSS1, HYPT2, PSS, PSS1 | 602593 |