| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72118164-72118425 | Common:2; Rare:82 | ||||
| chr15:72231080-72231516 | Common:3; Rare:136 | ||||
| chr15:72375951-72376103 | Common:2; Rare:66; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:73633189-73633595 | Common:2; Rare:161 | ||||
| chr15:73926322-73926476 | Rare:45 | ||||
| chr15:73994587-73994801 | Rare:46 | ||||
| chr15:74461100-74461314 | Rare:66 | ||||
| chr15:74540971-74541291 | Common:4; Rare:116 | ||||
| chr15:74843113-74843339 | Common:1; Rare:64 | ||||
| chr15:74906753-74906878 | Common:1; Rare:53 | ||||
| chr15:74938007-74938247 | Common:2; Rare:85 | ||||
| chr15:75201754-75201904 | Rare:46 | ||||
| chr15:75335973-75336091 | Common:1; Rare:53 | ||||
| chr15:75455802-75455935 | Rare:42 | ||||
| chr15:75625612-75625846 | Common:2; Rare:56 |