| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:18474003-18474195 | Rare:50 | ||||
| chr9:19049337-19049423 | Rare:35 | ||||
| chr9:33025071-33025304 | Common:6; Rare:96 | ||||
| chr9:33290377-33290565 | Common:2; Rare:71 | ||||
| chr9:34178952-34179058 | Common:1; Rare:28 | ||||
| chr9:34329195-34329593 | Rare:126 | ||||
| chr9:34620472-34620597 | Common:1; Rare:32 | ||||
| chr9:35657855-35658322 | Common:7; Rare:407; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35689761-35690114 | Common:4; Rare:113; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35732096-35732320 | Rare:65 | ||||
| chr9:35732373-35732631 | Common:2; Rare:63 | ||||
| chr9:36258404-36258607 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37904091-37904222 | Rare:40 | ||||
| chr9:65675700-65675957 | Rare:59 | ||||
| chr9:68779966-68780079 | Common:1; Rare:33 |