| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34329203-34329606 | Rare:127 | ||||
| chr9:34637725-34637950 | Rare:66 | ||||
| chr9:35072507-35072675 | Rare:46; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:35161773-35162062 | Common:4; Rare:82 | ||||
| chr9:35657970-35658389 | Common:7; Rare:312; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):34 | ||||
| chr9:35665187-35665361 | Common:2; Rare:65 | ||||
| chr9:35689861-35690102 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:35732083-35732334 | Common:2; Rare:70 | ||||
| chr9:35732373-35732684 | Common:3; Rare:79 | ||||
| chr9:35748982-35749377 | Common:2; Rare:146 | ||||
| chr9:35814983-35815231 | Rare:69 | ||||
| chr9:36190690-36191000 | Common:1; Rare:105 | ||||
| chr9:36258404-36258579 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37785004-37785115 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37904091-37904222 | Rare:40 |