| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:59372528-59372697 | Common:1; Rare:45 | ||||
| chr15:59372775-59373052 | Common:2; Rare:96 | ||||
| chr15:60397943-60398134 | Common:2; Rare:37 | ||||
| chr15:60479050-60479213 | Common:2; Rare:69 | ||||
| chr15:63042378-63042943 | Common:8; Rare:174; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63048335-63048677 | Common:4; Rare:130; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63189224-63189614 | Common:3; Rare:120 | ||||
| chr15:63277278-63277626 | Common:4; Rare:73 | ||||
| chr15:63504384-63504639 | Common:2; Rare:84 | ||||
| chr15:63833879-63834053 | Common:1; Rare:68 | ||||
| chr15:64093780-64094123 | Common:1; Rare:97 | ||||
| chr15:64151413-64151731 | Common:1; Rare:89 | ||||
| chr15:64162871-64163358 | Common:5; Rare:156; Clinvar:7; Clinvar (benign):5 | ||||
| chr15:64387670-64387857 | Common:2; Rare:64 | ||||
| chr15:64703122-64703411 | Common:2; Rare:108 |