| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99651544-99651666 | Common:2; Rare:21 | ||||
| chr7:99655510-99655703 | Rare:44 | ||||
| chr7:99658028-99658336 | Common:2; Rare:55 | ||||
| chr7:99658343-99658442 | Rare:24 | ||||
| chr7:99673373-99673678 | Common:2; Rare:40 | ||||
| chr7:99675949-99676051 | Rare:16 | ||||
| chr7:99761126-99761255 | Rare:19 | ||||
| chr7:99763853-99764148 | Common:1; Rare:64 | ||||
| chr7:99768388-99768605 | Common:1; Rare:75 | ||||
| chr7:99768642-99768761 | Common:1; Rare:17 | ||||
| chr7:99772592-99772829 | Rare:54 | ||||
| chr7:100113662-100113949 | Common:4; Rare:136; Clinvar (pathogenic):1 | ||||
| chr7:100222350-100222384 | Rare:8 | ||||
| chr7:100226837-100227067 | Rare:35 | ||||
| chr7:100335881-100336194 | Common:1; Rare:97 |