| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42035473-42035684 | Common:1; Rare:43 | ||||
| chr15:42046664-42046972 | Common:2; Rare:43 | ||||
| chr15:42057138-42057285 | Common:2; Rare:35 | ||||
| chr15:42057438-42057802 | Common:1; Rare:83 | ||||
| chr15:42392458-42392901 | Common:3; Rare:112; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr15:42890537-42890758 | Rare:17 | ||||
| chr15:43127807-43127967 | Rare:23 | ||||
| chr15:43877503-43877672 | Common:2; Rare:29 | ||||
| chr15:44287899-44288080 | Rare:35 | ||||
| chr15:44536057-44536157 | Common:1; Rare:16 | ||||
| chr15:44683387-44683499 | Rare:24 | ||||
| chr15:44707358-44707386 | Rare:6 | ||||
| chr15:44726776-44727116 | Common:3; Rare:48 | ||||
| chr15:44784334-44784474 | Common:1; Rare:23 | ||||
| chr15:44979694-44980005 | Common:1; Rare:52 |