| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116254058-116254222 | Common:4; Rare:44 | ||||
| chr6:122471762-122471921 | Common:2; Rare:47 | ||||
| chr6:127343349-127343551 | Common:1; Rare:39 | ||||
| chr6:136289779-136290024 | Common:1; Rare:107 | ||||
| chr6:138773651-138773795 | Common:1; Rare:66 | ||||
| chr6:143060724-143060919 | Common:7; Rare:67 | ||||
| chr6:143450778-143450884 | Common:1; Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:145814723-145814906 | Common:1; Rare:88 | ||||
| chr6:151452051-151452477 | Common:4; Rare:138 | ||||
| chr6:158168225-158168382 | Common:2; Rare:55 | ||||
| chr6:159727052-159727155 | Rare:34 | ||||
| chr6:159789553-159789947 | Common:3; Rare:134 | ||||
| chr7:1570018-1570142 | Common:1; Rare:41 | ||||
| chr7:2242178-2242241 | Common:2; Rare:39 | ||||
| chr7:6009029-6009277 | Common:3; Rare:95; Clinvar:3; Clinvar (benign):14 |