| ID: 127817805 | H3K4me1 hESC enhancer GRCh37_chr10:43781282-43781790 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43285834..43286342) | | |
| ID: 127817804 | H3K4me1 hESC enhancer GRCh37_chr10:43778224-43778748 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43282776..43283300) | | |
| ID: 127817803 | H3K4me1 hESC enhancer GRCh37_chr10:43761143-43762018 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43265695..43266570) | | |
| ID: 127817802 | H3K4me1 hESC enhancer GRCh37_chr10:43754815-43755598 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43259367..43260150) | | |
| ID: 127817801 | H3K4me1 hESC enhancer GRCh37_chr10:43745585-43746376 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43250137..43250928) | | |
| ID: 127817800 | H3K4me1 hESC enhancer GRCh37_chr10:43744792-43745584 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43249344..43250136) | | |
| ID: 127817799 | H3K4me1 hESC enhancer GRCh37_chr10:43726130-43726684 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43230682..43231236) | | |
| ID: 127817798 | H3K4me1 hESC enhancer GRCh37_chr10:43723488-43724298 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43228040..43228850) | | |
| ID: 127817797 | H3K4me1 hESC enhancer GRCh37_chr10:43712515-43713270 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43217067..43217822) | | |
| ID: 127817796 | H3K4me1 hESC enhancer GRCh37_chr10:43711759-43712514 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43216311..43217066) | | |
| ID: 127817795 | H3K4me1 hESC enhancer GRCh37_chr10:43707013-43707615 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43211565..43212167) | | |
| ID: 127817794 | H3K4me1 hESC enhancer GRCh37_chr10:43700051-43700884 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43204603..43205436) | | |
| ID: 127817793 | H3K4me1 hESC enhancer GRCh37_chr10:43696895-43697396 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43201447..43201948) | | |
| ID: 126860919 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr10:43655229-43656428 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43159781..43160980) | | |
| ID: 118568825 | CSGALNACT2 divergent transcript [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43136824..43138393, complement) | | |
| ID: 107984225 | uncharacterized LOC107984225 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43230090..43232472) | | |
| ID: 221002 | RasGEF domain family member 1A [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43194535..43267065, complement) | CG4853 | 614531 |
| ID: 55454 | chondroitin sulfate N-acetylgalactosaminyltransferase 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43138445..43185308) | CHGN2, ChGn-2, GALNACT-2, GALNACT2, PRO0082, beta4GalNAcT | 616616 |