| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88058953-88059260 | Common:2; Rare:95 | ||||
| chr3:99817581-99817920 | Rare:99 | ||||
| chr3:99876142-99876276 | Common:1; Rare:32 | ||||
| chr3:108589422-108589704 | Common:3; Rare:69 | ||||
| chr3:112561607-112561706 | Rare:35 | ||||
| chr3:112561905-112562072 | Rare:54 | ||||
| chr3:113746789-113747071 | Common:4; Rare:63 | ||||
| chr3:114056492-114056801 | Common:2; Rare:117 | ||||
| chr3:119498375-119498578 | Common:4; Rare:66 | ||||
| chr3:120742511-120742772 | Common:2; Rare:73 | ||||
| chr3:121835048-121835209 | Common:2; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:122383199-122383345 | Common:2; Rare:42 | ||||
| chr3:122514878-122515026 | Common:1; Rare:38 | ||||
| chr3:122564243-122564443 | Common:3; Rare:62 | ||||
| chr3:123585036-123585317 | Common:1; Rare:85 |