| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100709207-100709716 | Common:9; Rare:153; Clinvar (benign):1 | ||||
| chr3:101513129-101513343 | Common:8; Rare:46 | ||||
| chr3:101561746-101561931 | Common:2; Rare:66 | ||||
| chr3:101573995-101574262 | Common:1; Rare:95 | ||||
| chr3:101724405-101724639 | Common:1; Rare:54 | ||||
| chr3:101779079-101779261 | Common:4; Rare:55 | ||||
| chr3:101779616-101779686 | Common:1; Rare:17 | ||||
| chr3:105366534-105366956 | Common:4; Rare:122 | ||||
| chr3:105367154-105367420 | Common:2; Rare:73 | ||||
| chr3:105868924-105869184 | Common:5; Rare:99 | ||||
| chr3:107522832-107523011 | Common:1; Rare:44 | ||||
| chr3:108222294-108222569 | Common:2; Rare:74 | ||||
| chr3:108589390-108589561 | Common:2; Rare:55 | ||||
| chr3:108589567-108589745 | Common:1; Rare:55 | ||||
| chr3:111859418-111859774 | Common:2; Rare:100 |