| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121161756-121161904 | Rare:33 | ||||
| chr9:121201097-121201150 | Common:1; Rare:17 | ||||
| chr9:121269040-121269109 | Rare:9 | ||||
| chr9:121289157-121289394 | Rare:53 | ||||
| chr9:121289784-121290101 | Common:2; Rare:54 | ||||
| chr9:121318668-121319159 | Common:2; Rare:143; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:121324266-121324644 | Common:2; Rare:77 | ||||
| chr9:121324650-121324923 | Common:4; Rare:59 | ||||
| chr9:121331288-121331446 | Rare:30 | ||||
| chr9:121332252-121332645 | Common:4; Rare:100; Clinvar (benign):2 | ||||
| chr9:121341365-121341473 | Rare:25 | ||||
| chr9:121467914-121467924 | Rare:2 | ||||
| chr9:121479241-121479275 | Rare:3 | ||||
| chr9:121479291-121479391 | Common:2; Rare:6 | ||||
| chr9:121499650-121499827 | Rare:55 |