| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34248977-34249242 | Common:1; Rare:58 | ||||
| chr6:34392265-34392665 | Rare:151 | ||||
| chr6:34425984-34426155 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696142-34696433 | Common:1; Rare:46 | ||||
| chr6:34696437-34696517 | Rare:14 | ||||
| chr6:34696590-34697008 | Common:1; Rare:107 | ||||
| chr6:34756982-34757115 | Common:1; Rare:21 | ||||
| chr6:34757320-34757556 | Common:1; Rare:69 | ||||
| chr6:34887922-34888124 | Common:1; Rare:56 | ||||
| chr6:34889143-34889277 | Common:1; Rare:33 | ||||
| chr6:35213601-35214071 | Common:1; Rare:111 | ||||
| chr6:35214162-35214436 | Common:2; Rare:73 | ||||
| chr6:35259365-35259797 | Common:3; Rare:134 | ||||
| chr6:35468254-35468462 | Common:3; Rare:82 | ||||
| chr6:35688809-35688950 | Rare:53 |