| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12004284-12004428 | Common:2; Rare:46 | ||||
| chr3:12158907-12159048 | Rare:46 | ||||
| chr3:12287712-12287930 | Common:6; Rare:48 | ||||
| chr3:12484371-12484606 | Common:2; Rare:64; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12663489-12663666 | Common:4; Rare:53 | ||||
| chr3:12664027-12664345 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:12796435-12796786 | Common:5; Rare:90 | ||||
| chr3:12797013-12797188 | Common:2; Rare:29 | ||||
| chr3:12840439-12840528 | Rare:26 | ||||
| chr3:12841492-12841826 | Common:2; Rare:116 | ||||
| chr3:13420162-13420443 | Common:1; Rare:84 | ||||
| chr3:13480060-13480339 | Common:1; Rare:66 | ||||
| chr3:14124723-14125173 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178881 | Common:2; Rare:169; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402487-14402695 | Rare:50 |