| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:187742018-187742261 | Common:2; Rare:47 | ||||
| chr3:187742398-187742416 | Rare:1 | ||||
| chr3:187742439-187742712 | Common:1; Rare:49 | ||||
| chr3:187742802-187743073 | Common:3; Rare:63 | ||||
| chr3:187743089-187743345 | Rare:55 | ||||
| chr3:187744406-187744689 | Common:3; Rare:115 | ||||
| chr3:188266079-188266285 | Rare:39 | ||||
| chr3:188854031-188854084 | Rare:11 | ||||
| chr3:188951066-188951170 | Rare:18 | ||||
| chr3:189099095-189099491 | Rare:93 | ||||
| chr3:191380096-191380192 | Common:4; Rare:29; Clinvar (benign):2 | ||||
| chr3:192515234-192515423 | Common:2; Rare:43 | ||||
| chr3:194583888-194584027 | Common:11; Rare:48 | ||||
| chr3:195657920-195658137 | Common:12; Rare:37 | ||||
| chr3:197627806-197628006 | Common:6; Rare:70 |