| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72118731-72118862 | Common:2; Rare:22 | ||||
| chr15:72231120-72231720 | Common:6; Rare:181 | ||||
| chr15:72272714-72273002 | Common:3; Rare:74 | ||||
| chr15:72320137-72320349 | Common:1; Rare:69 | ||||
| chr15:72375919-72376176 | Common:3; Rare:99; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72473681-72473833 | Common:1; Rare:25 | ||||
| chr15:72474153-72474402 | Rare:93 | ||||
| chr15:72686108-72686468 | Common:2; Rare:115; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:72783666-72783917 | Common:2; Rare:112 | ||||
| chr15:72784270-72784600 | Common:5; Rare:50 | ||||
| chr15:73051077-73051874 | Common:8; Rare:301 | ||||
| chr15:73051924-73052176 | Common:1; Rare:77 | ||||
| chr15:73052731-73052881 | Rare:50 | ||||
| chr15:73633228-73633613 | Common:2; Rare:149 | ||||
| chr15:73684059-73684447 | Rare:106 |