| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136275668-136275985 | Common:1; Rare:133 | ||||
| chr6:137218046-137218332 | Common:2; Rare:52 | ||||
| chr6:137218705-137218815 | Rare:18 | ||||
| chr6:137868151-137868236 | Rare:15 | ||||
| chr6:138464021-138464066 | Rare:8 | ||||
| chr6:144286386-144286450 | Common:1; Rare:11 | ||||
| chr6:145890794-145890966 | Common:2; Rare:34 | ||||
| chr6:148507848-148508088 | Common:3; Rare:44 | ||||
| chr6:150683353-150683625 | Common:1; Rare:50 | ||||
| chr6:157954232-157954413 | Rare:34 | ||||
| chr6:158232988-158233146 | Rare:34 | ||||
| chr6:158303272-158303383 | Rare:25 | ||||
| chr6:158627986-158628164 | Common:2; Rare:48 | ||||
| chr6:158752107-158752388 | Rare:50 | ||||
| chr6:158767064-158767509 | Common:4; Rare:186; Clinvar:2; Clinvar (benign):3 |