| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113463545-113463800 | Common:2; Rare:86 | ||||
| chr9:114387949-114388111 | Common:1; Rare:51 | ||||
| chr9:115117985-115118188 | Common:3; Rare:47 | ||||
| chr9:115118193-115118252 | Rare:12 | ||||
| chr9:116687221-116687361 | Common:3; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793237-120793475 | Common:1; Rare:83 | ||||
| chr9:120842901-120843283 | Common:1; Rare:123 | ||||
| chr9:120868818-120869069 | Common:2; Rare:55 | ||||
| chr9:120929091-120929202 | Common:3; Rare:26 | ||||
| chr9:121074819-121074981 | Rare:81 | ||||
| chr9:121075104-121075240 | Rare:33 | ||||
| chr9:121201829-121202151 | Common:2; Rare:96 | ||||
| chr9:121268000-121268214 | Common:1; Rare:71 | ||||
| chr9:121281640-121281892 | Rare:68 | ||||
| chr9:121286007-121286146 | Common:1; Rare:37 |