| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:24494722-24494909 | Rare:50 | ||||
| chr3:24494927-24495255 | Common:2; Rare:92 | ||||
| chr3:25428103-25428398 | Rare:67 | ||||
| chr3:25428406-25428731 | Common:1; Rare:71 | ||||
| chr3:25664874-25665127 | Common:2; Rare:86 | ||||
| chr3:25783371-25783641 | Common:2; Rare:91; Clinvar (benign):3 | ||||
| chr3:25790008-25790126 | Common:4; Rare:45 | ||||
| chr3:28241538-28241660 | Common:1; Rare:41 | ||||
| chr3:28348471-28348747 | Common:1; Rare:60 | ||||
| chr3:28348756-28349253 | Common:4; Rare:168 | ||||
| chr3:29280831-29281433 | Common:15; Rare:115 | ||||
| chr3:29281768-29282048 | Common:1; Rare:66 | ||||
| chr3:30606296-30606554 | Common:1; Rare:65; Clinvar:2 | ||||
| chr3:30606572-30606975 | Common:1; Rare:123; Clinvar:7; Clinvar (benign):7 | ||||
| chr3:31532077-31532168 | Common:2; Rare:26 |