| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72736528-72736815 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr15:73927684-73927860 | Common:1; Rare:52 | ||||
| chr15:80507142-80507472 | Common:6; Rare:48 | ||||
| chr15:82750453-82750591 | Common:2; Rare:35 | ||||
| chr15:83164044-83164359 | Common:2; Rare:53 | ||||
| chr15:90230990-90231098 | Common:1; Rare:37 | ||||
| chr15:96327307-96327582 | Common:3; Rare:38 | ||||
| chr15:96331474-96331686 | Common:1; Rare:62 | ||||
| chr15:96337149-96337489 | Common:5; Rare:95; Clinvar (pathogenic):1 | ||||
| chr15:98650852-98650920 | Rare:16 | ||||
| chr16:11841726-11841911 | Common:1; Rare:74 | ||||
| chr16:29809889-29810207 | Common:6; Rare:173 | ||||
| chr16:30875331-30875434 | Rare:28 | ||||
| chr16:64971456-64971598 | Common:2; Rare:29 | ||||
| chr16:67843921-67843969 | Rare:5 |