| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64387598-64387914 | Common:3; Rare:114 | ||||
| chr15:64460188-64460324 | Rare:32 | ||||
| chr15:64460525-64460595 | Rare:18 | ||||
| chr15:64460903-64460924 | Rare:1 | ||||
| chr15:64461135-64461275 | Common:1; Rare:24 | ||||
| chr15:64703122-64703514 | Common:2; Rare:139 | ||||
| chr15:64775562-64775788 | Common:4; Rare:40 | ||||
| chr15:64825470-64826075 | Common:4; Rare:106 | ||||
| chr15:64826077-64826243 | Rare:23 | ||||
| chr15:64841410-64841574 | Common:1; Rare:40 | ||||
| chr15:64841584-64841983 | Common:1; Rare:114 | ||||
| chr15:64911733-64911912 | Common:4; Rare:40 | ||||
| chr15:64989762-64990194 | Common:6; Rare:133; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:65029442-65029725 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:65133669-65134006 | Common:1; Rare:96 |