| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113746969-113747104 | Common:3; Rare:21 | ||||
| chr3:114056473-114056860 | Common:2; Rare:142 | ||||
| chr3:114624186-114624323 | Rare:18 | ||||
| chr3:114624910-114625048 | Common:1; Rare:18 | ||||
| chr3:119294060-119294465 | Rare:84; Clinvar:1 | ||||
| chr3:119468837-119469009 | Rare:63 | ||||
| chr3:120094276-120094570 | Common:3; Rare:107 | ||||
| chr3:120450902-120451085 | Rare:63 | ||||
| chr3:120596122-120596451 | Common:2; Rare:128 | ||||
| chr3:120742503-120742783 | Common:2; Rare:78 | ||||
| chr3:121545939-121546059 | Common:1; Rare:36 | ||||
| chr3:121749646-121749994 | Common:1; Rare:79 | ||||
| chr3:121834983-121835248 | Common:3; Rare:91; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383183-122383323 | Common:1; Rare:43 | ||||
| chr3:122384068-122384227 | Rare:60 |