| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122383180-122383354 | Common:2; Rare:53 | ||||
| chr3:122384011-122384268 | Rare:91 | ||||
| chr3:122514873-122514997 | Common:1; Rare:38 | ||||
| chr3:122564147-122564231 | Common:1; Rare:20 | ||||
| chr3:122564281-122564421 | Common:1; Rare:41 | ||||
| chr3:122793773-122793917 | Common:3; Rare:38 | ||||
| chr3:123201815-123201967 | Common:1; Rare:49 | ||||
| chr3:123585023-123585317 | Common:1; Rare:91 | ||||
| chr3:123585491-123585590 | Rare:19 | ||||
| chr3:124730324-124730474 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:125375236-125375426 | Rare:57 | ||||
| chr3:125520129-125520297 | Rare:61 | ||||
| chr3:126084099-126084236 | Common:1; Rare:59 | ||||
| chr3:126703965-126704302 | Common:4; Rare:102 | ||||
| chr3:127598223-127598467 | Common:3; Rare:73 |