| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64381383-64381763 | Common:1; Rare:88 | ||||
| chr15:64387592-64387936 | Common:3; Rare:120 | ||||
| chr15:64460159-64460354 | Rare:45 | ||||
| chr15:64460414-64460628 | Rare:55 | ||||
| chr15:64460896-64461040 | Common:1; Rare:10 | ||||
| chr15:64461163-64461385 | Common:2; Rare:34 | ||||
| chr15:64703143-64703553 | Common:3; Rare:139 | ||||
| chr15:64825494-64825926 | Common:4; Rare:76 | ||||
| chr15:64841298-64842004 | Common:2; Rare:182 | ||||
| chr15:64911698-64911924 | Common:4; Rare:53 | ||||
| chr15:64989433-64989581 | Common:1; Rare:24 | ||||
| chr15:64989746-64990269 | Common:7; Rare:160; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:65029436-65029718 | Common:4; Rare:99; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:65133566-65133995 | Common:1; Rare:136 | ||||
| chr15:65184454-65184628 | Rare:51 |