| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:19946974-19947412 | Common:5; Rare:164 | ||||
| chr3:20186176-20186418 | Common:2; Rare:77 | ||||
| chr3:23202926-23203198 | Common:1; Rare:98 | ||||
| chr3:23916863-23917204 | Rare:132 | ||||
| chr3:23917645-23918031 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr3:24494725-24494880 | Rare:38 | ||||
| chr3:25428098-25428284 | Rare:34 | ||||
| chr3:25783392-25783627 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr3:25790008-25790118 | Common:3; Rare:42 | ||||
| chr3:28241433-28241683 | Common:1; Rare:85 | ||||
| chr3:28348592-28348639 | Rare:9 | ||||
| chr3:28348644-28348741 | Rare:21 | ||||
| chr3:28348762-28349185 | Common:3; Rare:136 | ||||
| chr3:29280864-29281081 | Common:3; Rare:41 | ||||
| chr3:31532383-31532654 | Common:4; Rare:75 |