| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:58749592-58750063 | Common:4; Rare:149 | ||||
| chr15:58770987-58771317 | Common:3; Rare:132 | ||||
| chr15:59372794-59373038 | Common:2; Rare:79 | ||||
| chr15:59689270-59689456 | Common:7; Rare:106 | ||||
| chr15:60479060-60479207 | Common:2; Rare:61 | ||||
| chr15:63042445-63042832 | Common:6; Rare:129; Clinvar:5; Clinvar (benign):2 | ||||
| chr15:63157411-63157563 | Common:2; Rare:67 | ||||
| chr15:63189316-63189627 | Common:2; Rare:103 | ||||
| chr15:63277373-63277626 | Common:3; Rare:48 | ||||
| chr15:63504373-63504734 | Common:2; Rare:124 | ||||
| chr15:64093780-64094127 | Common:1; Rare:98 | ||||
| chr15:64162939-64163286 | Common:4; Rare:117; Clinvar:6; Clinvar (benign):4 | ||||
| chr15:64381424-64381666 | Rare:46 | ||||
| chr15:64387670-64387876 | Common:2; Rare:78 | ||||
| chr15:64989757-64990079 | Common:4; Rare:107; Clinvar:2; Clinvar (benign):1 |