| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:73624142-73624477 | Common:5; Rare:102 | ||||
| chr3:75785500-75785702 | Common:4; Rare:27 | ||||
| chr3:75906581-75906839 | Common:2; Rare:73 | ||||
| chr3:77039967-77040155 | Common:1; Rare:47 | ||||
| chr3:79018997-79019023 | Rare:7 | ||||
| chr3:81761446-81761801 | Common:8; Rare:127; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:87227186-87227417 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058186-88058539 | Common:1; Rare:89 | ||||
| chr3:88058837-88059332 | Common:5; Rare:181 | ||||
| chr3:88149617-88149750 | Rare:32 | ||||
| chr3:88149857-88150276 | Common:6; Rare:151 | ||||
| chr3:93979947-93980242 | Common:4; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062872-94063111 | Rare:64 | ||||
| chr3:94063351-94063462 | Rare:25 | ||||
| chr3:97439485-97439661 | Rare:26 |