| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39590129-39590406 | Common:2; Rare:40 | ||||
| chr15:39609238-39609445 | Rare:34 | ||||
| chr15:39629559-39629631 | Rare:17 | ||||
| chr15:40346269-40346484 | Common:2; Rare:49 | ||||
| chr15:40352738-40353065 | Common:3; Rare:67 | ||||
| chr15:40353777-40353809 | Rare:3 | ||||
| chr15:40354134-40354349 | Common:2; Rare:36 | ||||
| chr15:40354647-40354956 | Common:1; Rare:42 | ||||
| chr15:40845975-40846153 | Rare:26 | ||||
| chr15:40847482-40847561 | Common:1; Rare:23 | ||||
| chr15:40932736-40933034 | Common:1; Rare:56 | ||||
| chr15:41302646-41302785 | Common:1; Rare:40 | ||||
| chr15:41527906-41528189 | Common:1; Rare:71 | ||||
| chr15:44659170-44659474 | Rare:70; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:44726773-44727072 | Common:1; Rare:41 |