| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:98576760-98576841 | Common:1; Rare:18 | ||||
| chr13:98576970-98577427 | Common:3; Rare:147 | ||||
| chr13:98577482-98577728 | Common:1; Rare:67 | ||||
| chr13:98577849-98577926 | Rare:18 | ||||
| chr13:98978036-98978195 | Common:1; Rare:29 | ||||
| chr13:98978348-98978640 | Common:3; Rare:42 | ||||
| chr13:99086115-99086509 | Common:4; Rare:111 | ||||
| chr13:99086512-99086867 | Common:3; Rare:125 | ||||
| chr13:99200433-99200595 | Common:1; Rare:44 | ||||
| chr13:99200599-99200962 | Common:7; Rare:157 | ||||
| chr13:99201244-99201671 | Common:1; Rare:151 | ||||
| chr13:99501198-99501554 | Common:1; Rare:108 | ||||
| chr13:99501633-99501816 | Rare:74 | ||||
| chr13:99606640-99607093 | Common:4; Rare:164 | ||||
| chr13:99982155-99982451 | Rare:73; Clinvar:1; Clinvar (benign):2 |