| ID: 127405832 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31731027-31731582 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31763250..31763805) | | |
| ID: 127405831 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31707855-31708486 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31740078..31740709) | | |
| ID: 127405830 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31707224-31707854 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31739447..31740077) | | |
| ID: 127405829 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31704508-31705382 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31736731..31737605) | | |
| ID: 113174991 | MED14-independent group 3 enhancer GRCh37_chr6:31701615-31702814 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31733838..31735037) | | |
| ID: 106481919 | RNA, U6 small nuclear 850, pseudogene [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31756951..31757053, complement) | RNU6-1030P | |
| ID: 105375020 | uncharacterized LOC105375020 [Homo sapiens (human)] | | | |
| ID: 104413891 | SAPCD1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31764135..31765588, complement) | C6orf26-AS1 | |
| ID: 100532732 | MSH5-SAPCD1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31739948..31764850) | MSH5-C6orf26 | |
| ID: 401251 | suppressor APC domain containing 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31762656..31764850) | C6orf26, NG23 | |
| ID: 80740 | lymphocyte antigen 6 family member G6C [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31718648..31721746, complement) | C6orf24, G6c, NG24 | 610435 |
| ID: 80739 | megakaryocyte and platelet inhibitory receptor G6b [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31720296..31726714) | C6orf25, G6b, G6b-B, NG31, THAMY | 606520 |
| ID: 23564 | DDAH family member 2, ADMA-independent [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31727040..31730263, complement) | DDAH, DDAHII, G6a, HEL-S-277, NG30 | 604744 |
| ID: 4439 | mutS homolog 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31740005..31762676) | G7, MUTSH5, NG23, POF13, SPGF74 | 603382 |
| ID: 1192 | chloride intracellular channel 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31730581..31737318, complement) | CL1C1, CLCNL1, G6, NCC27 | 602872 |