| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:593848-594051 | Common:3; Rare:46 | ||||
| chr9:738043-738387 | Common:3; Rare:134; Clinvar:1 | ||||
| chr9:2494679-2494763 | Common:1; Rare:21 | ||||
| chr9:2570667-2571031 | Common:3; Rare:74 | ||||
| chr9:2623579-2623677 | Common:1; Rare:25 | ||||
| chr9:5438471-5438553 | Common:2; Rare:17 | ||||
| chr9:13787646-13787808 | Common:1; Rare:53 | ||||
| chr9:14031250-14031385 | Rare:35 | ||||
| chr9:14316740-14317115 | Common:3; Rare:79 | ||||
| chr9:14993193-14993318 | Common:2; Rare:42 | ||||
| chr9:15486004-15486168 | Rare:50 | ||||
| chr9:18437501-18437795 | Common:2; Rare:59 | ||||
| chr9:20684746-20684975 | Rare:50 | ||||
| chr9:25677372-25677666 | Common:3; Rare:116 | ||||
| chr9:32550822-32551103 | Common:1; Rare:115; Clinvar:2; Clinvar (benign):2 |