| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70763405-70763715 | Common:4; Rare:190 | ||||
| chr15:70853219-70853382 | Rare:23 | ||||
| chr15:70854067-70854309 | Rare:134 | ||||
| chr15:70892304-70892880 | Common:3; Rare:201 | ||||
| chr15:72117722-72118435 | Common:8; Rare:365 | ||||
| chr15:72197758-72197944 | Common:3; Rare:75 | ||||
| chr15:72206744-72207279 | Common:4; Rare:201 | ||||
| chr15:72208351-72209250 | Common:10; Rare:342 | ||||
| chr15:72230120-72230680 | Common:6; Rare:273 | ||||
| chr15:72231044-72231529 | Common:6; Rare:289 | ||||
| chr15:72231543-72231738 | Common:4; Rare:79 | ||||
| chr15:72272469-72272929 | Common:3; Rare:208 | ||||
| chr15:72375864-72376171 | Common:6; Rare:211; Clinvar:21; Clinvar (benign):4; Clinvar (pathogenic):11 | ||||
| chr15:72474161-72474731 | Common:1; Rare:284 | ||||
| chr15:72474710-72475070 | Common:3; Rare:191; Clinvar (benign):2 |