| ID: 127817991 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr10:50898489-50899090 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49690443..49691044) | | |
| ID: 127817990 | OCT4-NANOG hESC enhancer GRCh37_chr10:50897886-50898488 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49689840..49690442) | | |
| ID: 127817989 | H3K4me1 hESC enhancer GRCh37_chr10:50858633-50859483 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49650587..49651437) | | |
| ID: 127817988 | H3K4me1 hESC enhancer GRCh37_chr10:50856930-50857780 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49648884..49649734) | | |
| ID: 127817987 | H3K4me1 hESC enhancer GRCh37_chr10:50856078-50856929 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49648032..49648883) | | |
| ID: 127817986 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:50820225-50821122 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49612179..49613076) | | |
| ID: 127817985 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:50819328-50820224 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49611282..49612178) | | |
| ID: 127817984 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:50817489-50818283 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49609443..49610237) | | |
| ID: 127817983 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:50816693-50817488 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49608647..49609442) | | |
| ID: 127817982 | H3K4me1 hESC enhancer GRCh37_chr10:50803283-50803782 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49595237..49595736) | | |
| ID: 127817981 | H3K4me1 hESC enhancer GRCh37_chr10:50802781-50803282 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49594735..49595236) | | |
| ID: 127817980 | H3K4me1 hESC enhancer GRCh37_chr10:50801673-50802172 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49593627..49594126) | | |
| ID: 127817979 | H3K4me1 hESC enhancer GRCh37_chr10:50801171-50801672 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49593125..49593626) | | |
| ID: 113939916 | Sharpr-MPRA regulatory region 3429 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49606983..49607277) | | |
| ID: 109729125 | high mobility group box 1 pseudogene 50 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49551308..49552652) | | |
| ID: 282966 | chromosome 10 open reading frame 53 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49679651..49710261) | | |
| ID: 6572 | solute carrier family 18 member A3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49610310..49612720) | CMS21, VACHT | 600336 |
| ID: 2074 | ERCC excision repair 6, chromatin remodeling factor [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49434881..49539538, complement) | ARMD5, CKN2, COFS, COFS1, CSB, CSB-PGBD3, POF11, RAD26, UVSS1 | 609413 |
| ID: 1103 | choline O-acetyltransferase [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49609095..49667942) | CHOACTASE, CMS1A, CMS1A2, CMS6 | 118490 |