| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34425970-34426182 | Common:5; Rare:86; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696703-34696988 | Common:1; Rare:65 | ||||
| chr6:34757302-34757554 | Common:1; Rare:72 | ||||
| chr6:34791992-34792136 | Common:3; Rare:45 | ||||
| chr6:35213543-35214068 | Common:1; Rare:120 | ||||
| chr6:35214280-35214436 | Common:1; Rare:43 | ||||
| chr6:35259378-35259797 | Common:3; Rare:132 | ||||
| chr6:35468228-35468451 | Common:3; Rare:80 | ||||
| chr6:35921042-35921271 | Common:1; Rare:93 | ||||
| chr6:36442870-36443087 | Common:2; Rare:86 | ||||
| chr6:36547334-36547593 | Common:1; Rare:113 | ||||
| chr6:36594122-36594382 | Common:4; Rare:99 | ||||
| chr6:36676320-36676533 | Common:2; Rare:31 | ||||
| chr6:36678500-36678748 | Common:1; Rare:64 | ||||
| chr6:36839438-36839566 | Common:1; Rare:16 |