| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:71130531-71130720 | Common:1; Rare:69; Clinvar:2 | ||||
| chr3:71360715-71360913 | Common:2; Rare:28 | ||||
| chr3:71581927-71582353 | Common:1; Rare:114 | ||||
| chr3:71582370-71582481 | Rare:36 | ||||
| chr3:71583630-71584095 | Common:2; Rare:164; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:71753570-71753705 | Common:3; Rare:65 | ||||
| chr3:71754756-71754832 | Rare:12 | ||||
| chr3:79018988-79019106 | Rare:37 | ||||
| chr3:81761432-81761828 | Common:8; Rare:139; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:86991091-86991330 | Common:1; Rare:60 | ||||
| chr3:87227032-87227477 | Common:3; Rare:123; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:87227634-87227704 | Rare:17 | ||||
| chr3:88058447-88058735 | Common:1; Rare:96 | ||||
| chr3:88058923-88059322 | Common:3; Rare:152 | ||||
| chr3:88149649-88149764 | Rare:24 |