| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106086213-106086390 | Rare:46 | ||||
| chr6:106325526-106325875 | Common:1; Rare:114 | ||||
| chr6:106629443-106629624 | Common:1; Rare:38 | ||||
| chr6:107957244-107957424 | Rare:38 | ||||
| chr6:107957901-107958407 | Common:2; Rare:159; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108260764-108260813 | Rare:13 | ||||
| chr6:108260913-108261308 | Common:2; Rare:162 | ||||
| chr6:109094832-109095188 | Common:4; Rare:107 | ||||
| chr6:109382208-109382624 | Common:5; Rare:170; Clinvar (benign):2 | ||||
| chr6:109440604-109440965 | Common:2; Rare:117 | ||||
| chr6:109449780-109450083 | Common:3; Rare:79 | ||||
| chr6:109452213-109452617 | Common:3; Rare:150 | ||||
| chr6:109455569-109455788 | Common:3; Rare:57 | ||||
| chr6:109483138-109483280 | Rare:61 | ||||
| chr6:109691142-109691334 | Common:3; Rare:46; Clinvar:4; Clinvar (benign):3 |