| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120691278-120691336 | Rare:13 | ||||
| chr3:122442042-122442207 | Rare:30 | ||||
| chr3:122725769-122725840 | Rare:16 | ||||
| chr3:123592917-123593244 | Common:2; Rare:45 | ||||
| chr3:123739961-123740258 | Common:3; Rare:56; Clinvar:2; Clinvar (benign):5 | ||||
| chr3:123950119-123950230 | Rare:18 | ||||
| chr3:123950825-123951275 | Common:3; Rare:66 | ||||
| chr3:124773848-124773988 | Common:1; Rare:36 | ||||
| chr3:125362503-125362543 | Rare:8 | ||||
| chr3:125928581-125928663 | Common:1; Rare:13 | ||||
| chr3:125990503-125990586 | Common:3; Rare:26 | ||||
| chr3:128065813-128065903 | Rare:16 | ||||
| chr3:129387690-129387863 | Common:3; Rare:38 | ||||
| chr3:130960712-130960908 | Common:1; Rare:23 | ||||
| chr3:130991496-130991608 | Rare:20 |