| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70763403-70763703 | Common:2; Rare:99 | ||||
| chr15:70853936-70854263 | Rare:96 | ||||
| chr15:70892561-70892868 | Common:1; Rare:68 | ||||
| chr15:71547259-71547276 | Rare:4 | ||||
| chr15:72118167-72118423 | Common:2; Rare:79 | ||||
| chr15:72231123-72231520 | Common:3; Rare:127 | ||||
| chr15:72375951-72376103 | Common:2; Rare:66; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:72474215-72474333 | Rare:40 | ||||
| chr15:72686146-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633123-73633465 | Common:1; Rare:135 | ||||
| chr15:73926322-73926467 | Rare:42 | ||||
| chr15:73994587-73994801 | Rare:46 | ||||
| chr15:74202424-74202705 | Common:2; Rare:58 | ||||
| chr15:74202739-74202995 | Rare:62; Clinvar:2 | ||||
| chr15:74461106-74461323 | Rare:66 |