| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43776964-43777079 | Rare:33 | ||||
| chr15:43777114-43777409 | Rare:65 | ||||
| chr15:43826870-43827007 | Rare:48 | ||||
| chr15:44427434-44427699 | Rare:64 | ||||
| chr15:44536862-44537401 | Common:3; Rare:198 | ||||
| chr15:44663556-44663842 | Rare:142; Clinvar:11; Clinvar (benign):6 | ||||
| chr15:44711341-44711612 | Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44712001 | Rare:28 | ||||
| chr15:44728832-44729188 | Common:1; Rare:72 | ||||
| chr15:45378494-45378658 | Common:3; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr15:45587156-45587668 | Common:1; Rare:157; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:45634921-45635090 | Rare:48 | ||||
| chr15:47717195-47717522 | Common:1; Rare:70 | ||||
| chr15:48331383-48331461 | Rare:26 | ||||
| chr15:48645685-48645938 | Common:2; Rare:80; Clinvar (benign):1 |