| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89135679-89135808 | Common:1; Rare:20 | ||||
| chr15:89176225-89176531 | Common:1; Rare:52 | ||||
| chr15:89177659-89177737 | Common:3; Rare:15 | ||||
| chr15:89663039-89663216 | Common:1; Rare:27 | ||||
| chr15:90076126-90076236 | Common:1; Rare:16 | ||||
| chr15:90084885-90085141 | Rare:83; Clinvar:2 | ||||
| chr15:90085273-90085602 | Common:5; Rare:70; Clinvar:2; Clinvar (benign):3 | ||||
| chr15:90088359-90088620 | Common:1; Rare:89; Clinvar (benign):1 | ||||
| chr15:90211937-90212317 | Common:5; Rare:72 | ||||
| chr15:90877003-90877211 | Common:1; Rare:55 | ||||
| chr15:92820380-92820556 | Rare:46 | ||||
| chr15:92882385-92882743 | Common:3; Rare:115 | ||||
| chr15:92952988-92953310 | Common:1; Rare:53 | ||||
| chr15:93000318-93000637 | Rare:73; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr15:93002059-93002282 | Common:2; Rare:49; Clinvar (benign):6; Clinvar (pathogenic):2 |