| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14943433-14943505 | Rare:20 | ||||
| chr3:40453163-40453422 | Common:6; Rare:57 | ||||
| chr3:47871018-47871179 | Rare:42 | ||||
| chr3:71064148-71064292 | Common:2; Rare:32 | ||||
| chr3:75435097-75435386 | Common:3; Rare:97 | ||||
| chr3:75641103-75641279 | Rare:29 | ||||
| chr3:75671712-75671795 | Common:1; Rare:1 | ||||
| chr3:81761515-81761571 | Common:4; Rare:13; Clinvar (benign):1 | ||||
| chr3:101576981-101576991 | |||||
| chr3:101676308-101676507 | Rare:66 | ||||
| chr3:107240586-107240800 | Rare:84 | ||||
| chr3:157174861-157175223 | Common:3; Rare:157 | ||||
| chr3:165192636-165192791 | Common:1; Rare:30 | ||||
| chr3:169765038-169765181 | Rare:64; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:181056341-181056627 | Rare:27 |