| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:58987894-58988174 | Common:3; Rare:82 | ||||
| chr15:59372541-59372641 | Common:1; Rare:21 | ||||
| chr15:59372692-59373028 | Common:3; Rare:113 | ||||
| chr15:59689182-59689456 | Common:7; Rare:129 | ||||
| chr15:60397901-60398133 | Common:2; Rare:52 | ||||
| chr15:60479031-60479207 | Common:2; Rare:76 | ||||
| chr15:63042440-63042940 | Common:6; Rare:154; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63048242-63048589 | Common:5; Rare:137; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:63157402-63157550 | Common:2; Rare:64 | ||||
| chr15:63189316-63189648 | Common:2; Rare:111 | ||||
| chr15:63277320-63277638 | Common:3; Rare:63 | ||||
| chr15:63504373-63504827 | Common:2; Rare:151 | ||||
| chr15:63833903-63834020 | Common:1; Rare:47 | ||||
| chr15:64093780-64094304 | Common:3; Rare:128 | ||||
| chr15:64151407-64151739 | Common:1; Rare:92 |