| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119498349-119498958 | Common:5; Rare:211 | ||||
| chr3:119660335-119660692 | Common:5; Rare:74 | ||||
| chr3:119660836-119661129 | Rare:47 | ||||
| chr3:120094341-120094514 | Common:1; Rare:69 | ||||
| chr3:120450791-120451105 | Common:2; Rare:104 | ||||
| chr3:120596180-120596492 | Common:1; Rare:121 | ||||
| chr3:120742503-120742777 | Common:2; Rare:77 | ||||
| chr3:121545941-121546080 | Common:1; Rare:41 | ||||
| chr3:121592993-121593115 | Rare:22 | ||||
| chr3:121593230-121593524 | Common:1; Rare:47 | ||||
| chr3:121749140-121749293 | Rare:27 | ||||
| chr3:121749463-121749522 | Rare:12 | ||||
| chr3:121749647-121750036 | Common:1; Rare:90 | ||||
| chr3:121834977-121835254 | Common:3; Rare:95; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383178-122383345 | Common:2; Rare:51 |