| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122383190-122383351 | Common:2; Rare:49 | ||||
| chr3:122384122-122384268 | Rare:59 | ||||
| chr3:122564264-122564441 | Common:1; Rare:55 | ||||
| chr3:122793755-122793859 | Common:2; Rare:35 | ||||
| chr3:123201617-123201962 | Common:1; Rare:90 | ||||
| chr3:123585043-123585317 | Common:1; Rare:82 | ||||
| chr3:123585502-123585553 | Rare:8 | ||||
| chr3:125375255-125375426 | Rare:50 | ||||
| chr3:125520149-125520288 | Rare:48 | ||||
| chr3:126704090-126704278 | Common:2; Rare:51 | ||||
| chr3:127598217-127598458 | Common:3; Rare:72 | ||||
| chr3:128052155-128052520 | Common:3; Rare:123 | ||||
| chr3:128123760-128124026 | Rare:73 | ||||
| chr3:128879434-128879675 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183806-129184069 | Common:2; Rare:88 |