| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43207333-43207552 | Rare:34 | ||||
| chr6:44249789-44250081 | Common:3; Rare:106 | ||||
| chr6:44251031-44251429 | Common:2; Rare:117 | ||||
| chr6:44251730-44252287 | Common:3; Rare:191 | ||||
| chr6:44253269-44253681 | Common:7; Rare:176 | ||||
| chr6:44253871-44254147 | Common:1; Rare:91 | ||||
| chr6:47606250-47606541 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr6:50133852-50133953 | Common:1; Rare:18 | ||||
| chr6:52420877-52421077 | Common:1; Rare:43 | ||||
| chr6:52664234-52664431 | Common:3; Rare:59 | ||||
| chr6:54367053-54367306 | Rare:50 | ||||
| chr6:56460129-56460496 | Common:1; Rare:74 | ||||
| chr6:56463072-56463233 | Rare:53; Clinvar:1 | ||||
| chr6:56463323-56463649 | Common:2; Rare:81 | ||||
| chr6:56579646-56579858 | Common:1; Rare:41 |