| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33264706-33265091 | Rare:103 | ||||
| chr9:34048873-34048971 | Rare:37 | ||||
| chr9:34329216-34329593 | Rare:117 | ||||
| chr9:34612078-34612223 | Common:8; Rare:50 | ||||
| chr9:34637739-34637927 | Rare:55 | ||||
| chr9:34652036-34652222 | Rare:55 | ||||
| chr9:35658018-35658337 | Common:6; Rare:210; Clinvar:15; Clinvar (benign):10; Clinvar (pathogenic):24 | ||||
| chr9:35685064-35685554 | Rare:125; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:35732079-35732356 | Common:2; Rare:83 | ||||
| chr9:35732369-35732711 | Common:3; Rare:85 | ||||
| chr9:35748985-35749316 | Common:2; Rare:113 | ||||
| chr9:35814998-35815275 | Rare:66 | ||||
| chr9:36258446-36258524 | Rare:18; Clinvar:1 | ||||
| chr9:36572773-36572941 | Rare:47 | ||||
| chr9:37800689-37800903 | Common:2; Rare:72 |