| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:134626520-134626951 | Common:2; Rare:141 | ||||
| chr9:134690551-134691057 | Common:6; Rare:236; Clinvar:12; Clinvar (benign):25 | ||||
| chr9:135126460-135126790 | Common:3; Rare:78 | ||||
| chr9:135130156-135130497 | Common:4; Rare:116 | ||||
| chr9:135134358-135134570 | Rare:113 | ||||
| chr9:135137490-135137921 | Common:2; Rare:157 | ||||
| chr9:135152650-135153051 | Common:7; Rare:152 | ||||
| chr9:135468887-135469181 | Common:2; Rare:68 | ||||
| chr9:136052510-136052890 | Common:5; Rare:98 | ||||
| chr9:136094040-136094319 | Common:1; Rare:115 | ||||
| chr9:136094300-136094510 | Common:3; Rare:95 | ||||
| chr9:136109151-136110056 | Common:16; Rare:356 | ||||
| chr9:136311624-136311860 | Common:1; Rare:63 | ||||
| chr9:136400116-136400370 | Common:5; Rare:156 | ||||
| chr9:136438939-136439099 | Rare:62; Clinvar (pathogenic):1 |