| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72375958-72376124 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:73926357-73926486 | Rare:36 | ||||
| chr15:73994587-73994716 | Rare:20 | ||||
| chr15:74202755-74202983 | Rare:59; Clinvar:2 | ||||
| chr15:74461107-74461314 | Rare:64 | ||||
| chr15:74541045-74541276 | Common:4; Rare:84 | ||||
| chr15:74615521-74615898 | Common:4; Rare:116 | ||||
| chr15:74826353-74826682 | Common:1; Rare:82 | ||||
| chr15:74843106-74843318 | Common:1; Rare:64 | ||||
| chr15:74995379-74995615 | Common:5; Rare:91 | ||||
| chr15:75451677-75451930 | Common:1; Rare:68 | ||||
| chr15:77420091-77420467 | Common:2; Rare:111 | ||||
| chr15:78149132-78149410 | Common:1; Rare:95 | ||||
| chr15:79923653-79923814 | Common:2; Rare:80 | ||||
| chr15:82262682-82262818 | Common:1; Rare:38 |