| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43776911-43777416 | Common:1; Rare:131 | ||||
| chr15:43824616-43824818 | Common:2; Rare:53 | ||||
| chr15:43826905-43827065 | Rare:70 | ||||
| chr15:44427031-44427230 | Common:1; Rare:54 | ||||
| chr15:44427255-44427653 | Common:1; Rare:98 | ||||
| chr15:44536852-44537192 | Common:1; Rare:119 | ||||
| chr15:44663591-44663845 | Rare:121; Clinvar:8; Clinvar (benign):4 | ||||
| chr15:44711314-44711611 | Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728869-44729140 | Common:1; Rare:54 | ||||
| chr15:45023052-45023233 | Common:3; Rare:47 | ||||
| chr15:45200489-45200658 | Common:1; Rare:48 | ||||
| chr15:45201106-45201132 | Common:1; Rare:14 | ||||
| chr15:45587110-45587274 | Rare:28 | ||||
| chr15:45587281-45587469 | Common:1; Rare:55; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:48330810-48331123 | Common:2; Rare:68 |