| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:84748265-84748644 | Rare:102 | ||||
| chr15:85380392-85380690 | Common:1; Rare:94 | ||||
| chr15:85543940-85544102 | Common:2; Rare:55 | ||||
| chr15:85582853-85583021 | Rare:37 | ||||
| chr15:85689765-85690101 | Common:2; Rare:75 | ||||
| chr15:85692955-85693448 | Common:2; Rare:125 | ||||
| chr15:88467363-88467746 | Common:5; Rare:115 | ||||
| chr15:88635519-88635672 | Rare:34 | ||||
| chr15:88636215-88636323 | Common:2; Rare:29 | ||||
| chr15:88638661-88639417 | Common:4; Rare:216 | ||||
| chr15:89088305-89088558 | Common:2; Rare:58 | ||||
| chr15:89243910-89244044 | Rare:42; Clinvar:3 | ||||
| chr15:89328694-89328994 | Common:1; Rare:96; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr15:89334787-89335069 | Common:3; Rare:107 | ||||
| chr15:89690692-89690761 | Common:1; Rare:23 |