| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:88534470-88535070 | Common:4; Rare:64 | ||||
| chr9:89310742-89311286 | Common:12; Rare:366 | ||||
| chr9:89318374-89318576 | Common:11; Rare:170 | ||||
| chr9:89318600-89319020 | Common:1; Rare:154 | ||||
| chr9:89498057-89498277 | Common:2; Rare:111 | ||||
| chr9:91361756-91362026 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr9:91423781-91424063 | Common:2; Rare:160 | ||||
| chr9:92115346-92115524 | Common:1; Rare:51; Clinvar:1 | ||||
| chr9:92293561-92293985 | Common:13; Rare:232 | ||||
| chr9:92325250-92326022 | Common:16; Rare:381 | ||||
| chr9:92669977-92670429 | Common:2; Rare:256 | ||||
| chr9:92764798-92765186 | Common:4; Rare:207 | ||||
| chr9:92877926-92878214 | Common:4; Rare:132 | ||||
| chr9:93095440-93095880 | Common:24; Rare:218 | ||||
| chr9:93134206-93134373 | Common:4; Rare:100 |