| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34612079-34612238 | Common:8; Rare:58 | ||||
| chr9:34652010-34652207 | Rare:56 | ||||
| chr9:34665373-34665655 | Rare:92 | ||||
| chr9:34666024-34666130 | Common:1; Rare:21 | ||||
| chr9:34989587-34989754 | Rare:40 | ||||
| chr9:35072500-35072746 | Rare:62; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35103090-35103296 | Common:1; Rare:67 | ||||
| chr9:35161788-35162186 | Common:4; Rare:113 | ||||
| chr9:35162277-35162319 | Rare:12 | ||||
| chr9:35618354-35618671 | Common:3; Rare:72 | ||||
| chr9:35646823-35646981 | Common:1; Rare:36 | ||||
| chr9:35657836-35658409 | Common:12; Rare:466; Clinvar:44; Clinvar (benign):17; Clinvar (pathogenic):40 | ||||
| chr9:35665165-35665324 | Common:2; Rare:61 | ||||
| chr9:35689702-35690130 | Common:4; Rare:133; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35691067-35691212 | Common:1; Rare:29 |