| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13420150-13420463 | Common:3; Rare:232 | ||||
| chr3:13479216-13479686 | Common:2; Rare:162 | ||||
| chr3:13479896-13480515 | Common:11; Rare:380 | ||||
| chr3:14016900-14017290 | Common:2; Rare:62 | ||||
| chr3:14124164-14124564 | Common:5; Rare:146 | ||||
| chr3:14124678-14125203 | Common:11; Rare:409; Clinvar:20; Clinvar (benign):5 | ||||
| chr3:14177591-14178024 | Common:8; Rare:160 | ||||
| chr3:14178497-14178915 | Common:8; Rare:565; Clinvar:15; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr3:14402262-14402798 | Common:12; Rare:315 | ||||
| chr3:14402800-14403090 | Common:2; Rare:76 | ||||
| chr3:14651365-14651848 | Common:2; Rare:402 | ||||
| chr3:14947099-14947639 | Common:13; Rare:511 | ||||
| chr3:14947938-14948233 | Rare:284 | ||||
| chr3:14948211-14948728 | Common:6; Rare:439 | ||||
| chr3:15034110-15034510 | Common:5; Rare:121 |