| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:95434895-95435213 | Common:1; Rare:128; Clinvar (benign):1 | ||||
| chr7:96709772-96709915 | Rare:52 | ||||
| chr7:97117414-97117792 | Common:2; Rare:160 | ||||
| chr7:98252208-98252372 | Rare:37 | ||||
| chr7:99325801-99325963 | Common:1; Rare:64 | ||||
| chr7:99408536-99409081 | Common:3; Rare:154 | ||||
| chr7:99438691-99439002 | Common:1; Rare:101 | ||||
| chr7:99466127-99466287 | Rare:55 | ||||
| chr7:99472625-99472942 | Common:4; Rare:100 | ||||
| chr7:99500244-99500405 | Common:2; Rare:46 | ||||
| chr7:99505117-99505275 | Common:4; Rare:59 | ||||
| chr7:99552083-99552182 | Rare:36 | ||||
| chr7:99558507-99558715 | Common:2; Rare:72 | ||||
| chr7:99616810-99617013 | Common:2; Rare:71 | ||||
| chr7:100015504-100015635 | Common:1; Rare:34 |