| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158999618-158999983 | Common:1; Rare:149; Clinvar:4; Clinvar (benign):4 | ||||
| chr6:159693219-159693609 | Common:6; Rare:114 | ||||
| chr6:159726863-159727224 | Common:1; Rare:142 | ||||
| chr6:159727333-159727633 | Common:5; Rare:130 | ||||
| chr6:159762278-159762586 | Common:3; Rare:89 | ||||
| chr6:159789538-159789958 | Common:4; Rare:137 | ||||
| chr6:159790235-159790508 | Common:7; Rare:85 | ||||
| chr6:160991630-160991884 | Common:1; Rare:90 | ||||
| chr6:161273739-161273848 | Common:1; Rare:26 | ||||
| chr6:161273936-161274183 | Rare:43 | ||||
| chr6:162726975-162727184 | Common:3; Rare:49 | ||||
| chr6:162727724-162728070 | Common:3; Rare:106; Clinvar:1 | ||||
| chr6:163413275-163413546 | Common:1; Rare:72 | ||||
| chr6:166342505-166342695 | Common:4; Rare:78 | ||||
| chr6:166627535-166627709 | Rare:57 |