| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2245567-2245833 | Rare:90 | ||||
| chr6:3068249-3068610 | Common:1; Rare:116 | ||||
| chr6:3157512-3157681 | Common:6; Rare:62 | ||||
| chr6:3751711-3751766 | Rare:15 | ||||
| chr6:3751837-3752078 | Common:4; Rare:81 | ||||
| chr6:4021103-4021467 | Common:1; Rare:135 | ||||
| chr6:5003608-5003837 | Common:6; Rare:72 | ||||
| chr6:5260663-5261032 | Common:5; Rare:129; Clinvar (benign):4 | ||||
| chr6:5261271-5261577 | Common:9; Rare:80 | ||||
| chr6:7108587-7108665 | Rare:27 | ||||
| chr6:8435391-8435631 | Common:3; Rare:85 | ||||
| chr6:10412359-10412557 | Common:2; Rare:34 | ||||
| chr6:10694603-10694991 | Common:4; Rare:104 | ||||
| chr6:10722847-10723241 | Common:6; Rare:134 | ||||
| chr6:12012279-12012293 | Rare:3 |