| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:55916683-55916815 | Common:2; Rare:42 | ||||
| chr15:55993557-55993825 | Common:1; Rare:84 | ||||
| chr15:56733462-56733755 | Common:2; Rare:140 | ||||
| chr15:56918409-56918809 | Common:3; Rare:138 | ||||
| chr15:58770897-58771323 | Common:5; Rare:161 | ||||
| chr15:59104886-59105146 | Common:1; Rare:81 | ||||
| chr15:59372541-59372689 | Common:1; Rare:36 | ||||
| chr15:59372775-59373028 | Common:2; Rare:87 | ||||
| chr15:60479065-60479173 | Common:2; Rare:42 | ||||
| chr15:62060364-62060509 | Rare:59 | ||||
| chr15:62165281-62165378 | Rare:28 | ||||
| chr15:62390445-62390634 | Common:1; Rare:83 | ||||
| chr15:63042658-63042966 | Rare:93; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63048359-63048680 | Common:4; Rare:119; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63156478-63156795 | Common:1; Rare:77 |