| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144901400-144901708 | Common:1; Rare:88 | ||||
| chr8:145052085-145052494 | Common:11; Rare:101 | ||||
| chr9:178975-179320 | Common:5; Rare:54 | ||||
| chr9:2015048-2015387 | Common:3; Rare:100 | ||||
| chr9:2017497-2017787 | Rare:84 | ||||
| chr9:2621344-2621814 | Common:5; Rare:188; Clinvar:1 | ||||
| chr9:2621844-2622180 | Common:6; Rare:119; Clinvar:9; Clinvar (benign):3 | ||||
| chr9:2844043-2844338 | Common:5; Rare:109 | ||||
| chr9:3525779-3526119 | Common:1; Rare:129 | ||||
| chr9:3526428-3526541 | Common:1; Rare:57 | ||||
| chr9:4299934-4300257 | Common:5; Rare:126; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:4666345-4666520 | Common:1; Rare:44 | ||||
| chr9:4666522-4666541 | Rare:6 | ||||
| chr9:4679428-4679824 | Common:1; Rare:173 | ||||
| chr9:4741082-4741385 | Common:5; Rare:142 |