| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44728716-44729205 | Common:1; Rare:98 | ||||
| chr15:45114139-45114326 | Common:2; Rare:40 | ||||
| chr15:45129821-45130289 | Common:1; Rare:105 | ||||
| chr15:45138494-45138679 | Rare:33 | ||||
| chr15:45147145-45147658 | Rare:120 | ||||
| chr15:45147753-45147824 | Rare:14 | ||||
| chr15:45147975-45148374 | Common:1; Rare:107 | ||||
| chr15:45150480-45150726 | Common:3; Rare:58 | ||||
| chr15:45151685-45152044 | Common:1; Rare:109 | ||||
| chr15:45201124-45201153 | Rare:15 | ||||
| chr15:45378488-45378717 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr15:45402211-45402360 | Common:2; Rare:43 | ||||
| chr15:45587177-45587474 | Common:1; Rare:80; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:45587769-45587815 | Common:1; Rare:8 | ||||
| chr15:45634673-45634912 | Common:1; Rare:56 |