| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118893899-118894354 | Common:3; Rare:142 | ||||
| chr6:121334434-121334579 | Common:4; Rare:61 | ||||
| chr6:121435549-121435806 | Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:122471701-122471934 | Common:3; Rare:79 | ||||
| chr6:122788901-122789296 | Rare:68 | ||||
| chr6:122789491-122789794 | Common:1; Rare:79 | ||||
| chr6:125301680-125302202 | Common:12; Rare:167 | ||||
| chr6:125781059-125781201 | Rare:24 | ||||
| chr6:125899995-125900184 | Rare:37 | ||||
| chr6:125918877-125919462 | Common:1; Rare:152 | ||||
| chr6:125956633-125956983 | Common:1; Rare:94 | ||||
| chr6:125986361-125986789 | Common:1; Rare:137 | ||||
| chr6:126340192-126340202 | Rare:4 | ||||
| chr6:127118443-127118711 | Common:1; Rare:38 | ||||
| chr6:127118979-127119290 | Rare:86 |