| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121894343-121894498 | Common:1; Rare:40 | ||||
| chr3:122383183-122383283 | Common:1; Rare:34 | ||||
| chr3:122384054-122384268 | Rare:79 | ||||
| chr3:122416039-122416227 | Common:1; Rare:61 | ||||
| chr3:122514853-122515029 | Common:1; Rare:50 | ||||
| chr3:122564243-122564426 | Common:3; Rare:54 | ||||
| chr3:122793762-122793958 | Common:3; Rare:51 | ||||
| chr3:123201733-123201970 | Common:1; Rare:72 | ||||
| chr3:123585036-123585179 | Common:1; Rare:53 | ||||
| chr3:123585495-123585590 | Rare:19 | ||||
| chr3:123700975-123701293 | Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:124730376-124730474 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:125375236-125375422 | Rare:55 | ||||
| chr3:125520142-125520267 | Rare:47 | ||||
| chr3:126084098-126084450 | Common:3; Rare:109 |