| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:154733610-154733912 | Common:1; Rare:99 | ||||
| chr6:155314452-155314668 | Common:2; Rare:83 | ||||
| chr6:157323479-157323652 | Common:3; Rare:60 | ||||
| chr6:158168195-158168409 | Common:2; Rare:77; Clinvar:1 | ||||
| chr6:158644698-158644833 | Common:2; Rare:67 | ||||
| chr6:158649852-158650066 | Common:1; Rare:38 | ||||
| chr6:158818098-158818358 | Common:5; Rare:104 | ||||
| chr6:158819316-158819429 | Common:2; Rare:47 | ||||
| chr6:158999761-158999886 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159000130-159000301 | Common:1; Rare:44 | ||||
| chr6:159693144-159693624 | Common:6; Rare:148 | ||||
| chr6:159726918-159727039 | Common:1; Rare:53 | ||||
| chr6:159727057-159727181 | Rare:41 | ||||
| chr6:159727314-159727637 | Common:6; Rare:136 | ||||
| chr6:159761807-159762073 | Common:5; Rare:129 |