| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:92892916-92893128 | Common:2; Rare:45 | ||||
| chr15:92893175-92893310 | Common:2; Rare:30 | ||||
| chr15:92894709-92894886 | Common:1; Rare:46 | ||||
| chr15:92897657-92897701 | Rare:12 | ||||
| chr15:92897758-92897800 | Rare:5 | ||||
| chr15:92897846-92897923 | Common:2; Rare:12 | ||||
| chr15:92897988-92898181 | Common:2; Rare:31 | ||||
| chr15:92920736-92920792 | Rare:11 | ||||
| chr15:92932220-92932283 | Rare:8 | ||||
| chr15:92981387-92981726 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:92981857-92981975 | Rare:18 | ||||
| chr15:93000407-93000652 | Rare:59; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr15:96268266-96268442 | Common:2; Rare:35 | ||||
| chr15:96268568-96268625 | Rare:13 | ||||
| chr15:96285365-96285723 | Common:2; Rare:67 |