| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34329185-34329620 | Common:1; Rare:137 | ||||
| chr9:34458546-34458826 | Rare:64 | ||||
| chr9:34620457-34620575 | Common:1; Rare:35 | ||||
| chr9:34637715-34638153 | Common:3; Rare:113 | ||||
| chr9:34646519-34646804 | Common:1; Rare:91; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr9:34652001-34652223 | Rare:66 | ||||
| chr9:34665363-34665654 | Rare:94 | ||||
| chr9:35072461-35072884 | Rare:99; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35103048-35103204 | Common:1; Rare:62 | ||||
| chr9:35161773-35162119 | Common:4; Rare:99 | ||||
| chr9:35162262-35162338 | Rare:30 | ||||
| chr9:35657841-35658322 | Common:8; Rare:415; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35689840-35690120 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:35731955-35732334 | Common:2; Rare:97 | ||||
| chr9:35732358-35732676 | Common:2; Rare:81 |