| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:77429630-77430030 | Common:26; Rare:240 | ||||
| chr13:77430477-77430779 | Rare:47 | ||||
| chr13:77431529-77431751 | Common:1; Rare:24 | ||||
| chr13:77472037-77472437 | Common:6; Rare:110 | ||||
| chr13:77477990-77478697 | Common:12; Rare:256 | ||||
| chr13:77699626-77700026 | Common:3; Rare:63 | ||||
| chr13:77724092-77724492 | Common:2; Rare:94 | ||||
| chr13:77730050-77730330 | Rare:50 | ||||
| chr13:77898024-77898424 | Rare:154; Clinvar:2; Clinvar (benign):4 | ||||
| chr13:78201381-78202213 | Common:13; Rare:296 | ||||
| chr13:78399168-78399380 | Common:4; Rare:66 | ||||
| chr13:78420830-78421230 | Common:1; Rare:142 | ||||
| chr13:78596053-78596189 | Rare:57 | ||||
| chr13:78660040-78660550 | Common:2; Rare:117 | ||||
| chr13:79194280-79194700 | Rare:84 |