| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64841594-64841992 | Common:1; Rare:114 | ||||
| chr15:64911778-64911954 | Common:4; Rare:50 | ||||
| chr15:64989430-64989577 | Common:1; Rare:23 | ||||
| chr15:64989745-64990155 | Common:6; Rare:136; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:65028879-65029210 | Common:5; Rare:65 | ||||
| chr15:65029431-65029702 | Common:4; Rare:96; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:65044912-65045418 | Rare:95 | ||||
| chr15:65067947-65068196 | Common:1; Rare:58 | ||||
| chr15:65132920-65133356 | Rare:163 | ||||
| chr15:65133751-65133997 | Common:1; Rare:72 | ||||
| chr15:65184451-65184636 | Rare:53 | ||||
| chr15:65184923-65185213 | Common:4; Rare:127 | ||||
| chr15:65185268-65185775 | Common:2; Rare:187 | ||||
| chr15:65286396-65286474 | Rare:32 | ||||
| chr15:65286628-65286701 | Common:1; Rare:12 |