| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:79896897-79897243 | Common:4; Rare:119 | ||||
| chr15:79897465-79897577 | Common:1; Rare:25 | ||||
| chr15:79922987-79923390 | Common:4; Rare:173 | ||||
| chr15:79923409-79923463 | Rare:23 | ||||
| chr15:79923588-79924122 | Common:9; Rare:195 | ||||
| chr15:79970712-79970923 | Common:2; Rare:47 | ||||
| chr15:79971044-79971392 | Common:2; Rare:61 | ||||
| chr15:80059331-80059754 | Common:1; Rare:138 | ||||
| chr15:80060129-80060293 | Common:2; Rare:60 | ||||
| chr15:80152915-80153078 | Common:2; Rare:44; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:80694914-80695386 | Common:3; Rare:147 | ||||
| chr15:80989539-80989633 | Common:1; Rare:30 | ||||
| chr15:80989661-80990144 | Common:5; Rare:207 | ||||
| chr15:81000542-81000578 | Rare:5 | ||||
| chr15:81000682-81001260 | Common:2; Rare:170 |