| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43746263-43746692 | Common:2; Rare:171 | ||||
| chr15:43770161-43770276 | Rare:21 | ||||
| chr15:43776886-43777127 | Common:1; Rare:77 | ||||
| chr15:43824632-43824789 | Common:2; Rare:41 | ||||
| chr15:44427269-44427660 | Common:1; Rare:98 | ||||
| chr15:44536657-44536697 | Rare:6 | ||||
| chr15:44536852-44537235 | Common:3; Rare:141 | ||||
| chr15:44711301-44711612 | Rare:92; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711794-44711982 | Rare:35 | ||||
| chr15:45200483-45200656 | Common:1; Rare:50 | ||||
| chr15:45378482-45378725 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
| chr15:45397159-45397473 | Common:1; Rare:62 | ||||
| chr15:45402186-45402360 | Common:2; Rare:52 | ||||
| chr15:45586891-45587230 | Common:1; Rare:60 | ||||
| chr15:45587288-45587454 | Common:1; Rare:51; Clinvar:6; Clinvar (benign):1 |