| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185282838-185283003 | Common:1; Rare:45 | ||||
| chr3:185498975-185499172 | Rare:68 | ||||
| chr3:185586026-185586343 | Common:1; Rare:68 | ||||
| chr3:186783281-186783606 | Common:1; Rare:134 | ||||
| chr3:194135949-194136212 | Rare:66 | ||||
| chr3:195543221-195543473 | Common:3; Rare:97 | ||||
| chr3:195876698-195876932 | Common:3; Rare:89 | ||||
| chr3:196082080-196082259 | Common:2; Rare:70 | ||||
| chr3:196287686-196287831 | Common:1; Rare:46 | ||||
| chr3:196568527-196568641 | Common:1; Rare:28 | ||||
| chr3:197298580-197298689 | Rare:39 | ||||
| chr3:197749815-197749995 | Rare:73 | ||||
| chr3:197949894-197950298 | Common:4; Rare:121; Clinvar (benign):2 | ||||
| chr4:499149-499257 | Common:2; Rare:32 | ||||
| chr4:674248-674507 | Rare:120 |