| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70763389-70763840 | Common:2; Rare:141 | ||||
| chr15:70892403-70892711 | Common:1; Rare:68 | ||||
| chr15:72117966-72118425 | Common:5; Rare:157 | ||||
| chr15:72230204-72230474 | Rare:70 | ||||
| chr15:72231102-72231523 | Common:3; Rare:134 | ||||
| chr15:72375915-72376156 | Common:3; Rare:95; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72473984-72474357 | Rare:107 | ||||
| chr15:72475156-72475280 | Common:1; Rare:35 | ||||
| chr15:72686122-72686220 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:72783481-72783844 | Common:2; Rare:140 | ||||
| chr15:73633139-73633323 | Rare:75 | ||||
| chr15:73633325-73633446 | Common:1; Rare:48 | ||||
| chr15:73926382-73926466 | Rare:26 | ||||
| chr15:73994583-73994806 | Common:1; Rare:47 | ||||
| chr15:74433788-74434127 | Common:5; Rare:108 |