| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67543091-67543151 | Rare:14 | ||||
| chr15:67543568-67543789 | Common:2; Rare:33 | ||||
| chr15:68054011-68054453 | Rare:139 | ||||
| chr15:68054739-68054815 | Common:2; Rare:13 | ||||
| chr15:68054821-68054884 | Common:1; Rare:13 | ||||
| chr15:68229290-68229568 | Common:4; Rare:88; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr15:68229646-68229914 | Common:2; Rare:107; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:68257124-68257349 | Common:2; Rare:65 | ||||
| chr15:68277214-68277476 | Common:1; Rare:62 | ||||
| chr15:68277559-68278162 | Common:7; Rare:188 | ||||
| chr15:68278213-68278334 | Rare:40 | ||||
| chr15:68817559-68817965 | Common:3; Rare:121 | ||||
| chr15:68818151-68818295 | Common:1; Rare:56 | ||||
| chr15:68818374-68818924 | Common:4; Rare:162 | ||||
| chr15:68820367-68820518 | Rare:33 |