| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:81761635-81761735 | Common:1; Rare:37; Clinvar:1 | ||||
| chr3:86991070-86991287 | Common:1; Rare:58 | ||||
| chr3:87227221-87227424 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058186-88058458 | Common:1; Rare:61 | ||||
| chr3:88058917-88059320 | Common:3; Rare:156 | ||||
| chr3:88149613-88150043 | Common:6; Rare:130 | ||||
| chr3:94062897-94063093 | Rare:47 | ||||
| chr3:96814388-96814626 | Rare:86 | ||||
| chr3:97764496-97764569 | Rare:11 | ||||
| chr3:97764706-97764814 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821747-97822132 | Common:1; Rare:125 | ||||
| chr3:98522601-98522739 | Rare:32 | ||||
| chr3:98732492-98732532 | Rare:4 | ||||
| chr3:98732610-98732711 | Rare:22 | ||||
| chr3:99638423-99638634 | Common:1; Rare:48 |