| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34318759-34318933 | Common:2; Rare:39 | ||||
| chr15:34336366-34336499 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:34336996-34337281 | Common:2; Rare:69 | ||||
| chr15:34337674-34337841 | Rare:55 | ||||
| chr15:34337910-34338212 | Common:1; Rare:95 | ||||
| chr15:34343018-34343298 | Common:5; Rare:87; Clinvar:4; Clinvar (benign):2 | ||||
| chr15:34367104-34367469 | Common:3; Rare:130 | ||||
| chr15:34367471-34367938 | Rare:101 | ||||
| chr15:34437750-34437883 | Common:6; Rare:38 | ||||
| chr15:34582812-34583027 | Common:3; Rare:68 | ||||
| chr15:34583598-34583838 | Common:6; Rare:84 | ||||
| chr15:34584031-34584221 | Common:1; Rare:47 | ||||
| chr15:34588415-34588575 | Rare:45 | ||||
| chr15:34969614-34969967 | Common:6; Rare:100 | ||||
| chr15:34988002-34988118 | Rare:28 |