| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43510688-43510954 | Rare:85 | ||||
| chr15:43648834-43649025 | Common:2; Rare:78 | ||||
| chr15:43746282-43746702 | Common:2; Rare:169 | ||||
| chr15:43774739-43775055 | Rare:68 | ||||
| chr15:43776885-43777075 | Common:1; Rare:59 | ||||
| chr15:43777114-43777408 | Rare:65 | ||||
| chr15:43792724-43793092 | Rare:107 | ||||
| chr15:43826933-43827007 | Rare:28 | ||||
| chr15:44288394-44288743 | Common:38; Rare:216 | ||||
| chr15:44536663-44537425 | Common:3; Rare:246 | ||||
| chr15:44572696-44572925 | Common:3; Rare:70; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:44711346-44711612 | Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45023051-45023334 | Common:3; Rare:85 | ||||
| chr15:45129837-45130013 | Rare:39 | ||||
| chr15:45139126-45139438 | Rare:97 |