| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119463598-119463780 | Common:3; Rare:52 | ||||
| chr3:119468837-119469010 | Rare:63 | ||||
| chr3:119677344-119677519 | Common:1; Rare:61 | ||||
| chr3:120094429-120094790 | Common:4; Rare:115 | ||||
| chr3:120596140-120596451 | Common:2; Rare:119 | ||||
| chr3:120742511-120742777 | Common:2; Rare:74 | ||||
| chr3:120908029-120908244 | Rare:59 | ||||
| chr3:121545980-121546059 | Common:1; Rare:20 | ||||
| chr3:121834983-121835234 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383283 | Common:1; Rare:32 | ||||
| chr3:122384054-122384268 | Rare:79 | ||||
| chr3:122416053-122416250 | Rare:64 | ||||
| chr3:122564261-122564422 | Common:2; Rare:48 | ||||
| chr3:123201858-123201967 | Common:1; Rare:36 | ||||
| chr3:123585028-123585284 | Common:1; Rare:81 |