| ID: 129661707 | ReSE screen-validated silencer GRCh37_chr6:31759127-31759287 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31791350..31791510) | | |
| ID: 127405833 | H3K27ac hESC enhancer GRCh37_chr6:31763127-31763981 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31795350..31796204) | | |
| 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: 126859651 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr6:31759783-31760982 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31792006..31793205) | | |
| ID: 121132678 | Sharpr-MPRA regulatory regions 3149 and 4553 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31772872..31773186) | | |
| 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: 102060414 | C2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31934474..31941724, complement) | | |
| ID: 100532732 | MSH5-SAPCD1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31739948..31764850) | MSH5-C6orf26 | |
| ID: 100130756 | ubiquinol-cytochrome c reductase hinge protein pseudogene 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31611083..31611356, complement) | Em:AF129756.18, UQCRHP5 | |
| ID: 401251 | suppressor APC domain containing 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31762656..31764850) | C6orf26, NG23 | |
| ID: 80737 | von Willebrand factor A domain containing 7 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31765590..31777328, complement) | C6orf27, G7c, NG37 | 609693 |
| ID: 57819 | LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31797396..31806966, complement) | C6orf28, G7B, YBL026W, snRNP | 607282 |
| 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: 7407 | valyl-tRNA synthetase 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31777518..31795752, complement) | G7A, NDMSCA, VARS, VARS2 | 192150 |