| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12560630-12560813 | Rare:29 | ||||
| chr3:12663625-12663937 | Common:5; Rare:81; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:12664027-12664423 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:12841433-12841951 | Common:2; Rare:156 | ||||
| chr3:12967717-12968013 | Common:4; Rare:105 | ||||
| chr3:12994989-12995248 | Common:1; Rare:61 | ||||
| chr3:13073411-13073584 | Common:5; Rare:56 | ||||
| chr3:13419818-13419993 | Common:2; Rare:42 | ||||
| chr3:13420137-13420537 | Common:1; Rare:123 | ||||
| chr3:13479945-13480337 | Common:3; Rare:98 | ||||
| chr3:14124223-14124472 | Common:3; Rare:62 | ||||
| chr3:14124581-14124679 | Common:1; Rare:34 | ||||
| chr3:14124694-14125166 | Common:4; Rare:139; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14125205-14125336 | Common:1; Rare:40 | ||||
| chr3:14177790-14178121 | Common:2; Rare:68 |