| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:104959538-104959597 | Rare:13 | ||||
| chr6:106971775-106971909 | Common:1; Rare:16 | ||||
| chr6:106972332-106972385 | Common:1; Rare:7 | ||||
| chr6:107115869-107115978 | Common:1; Rare:31 | ||||
| chr6:107116161-107116262 | Rare:31 | ||||
| chr6:107458994-107459049 | Rare:19; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:107829424-107829555 | Common:1; Rare:13 | ||||
| chr6:108004417-108004647 | Common:3; Rare:33 | ||||
| chr6:108781427-108781760 | Common:2; Rare:62 | ||||
| chr6:109109682-109109713 | Rare:11 | ||||
| chr6:109167537-109167747 | Common:4; Rare:50 | ||||
| chr6:109251251-109251468 | Common:3; Rare:53 | ||||
| chr6:113858767-113858914 | Rare:30 | ||||
| chr6:114082007-114082203 | Rare:31 | ||||
| chr6:114340967-114341325 | Common:5; Rare:59 |