| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143281630-143281799 | Common:3; Rare:41 | ||||
| chr8:143874252-143874537 | Common:3; Rare:76 | ||||
| chr8:143929956-143930249 | Common:3; Rare:126; Clinvar:17; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr8:143934892-143935203 | Common:1; Rare:127; Clinvar:8; Clinvar (benign):12 | ||||
| chr8:144313648-144314332 | Common:6; Rare:300 | ||||
| chr8:144700499-144700686 | Common:2; Rare:41 | ||||
| chr8:145002816-145003038 | Common:2; Rare:82 | ||||
| chr9:684139-684336 | Common:5; Rare:54 | ||||
| chr9:686515-686809 | Common:4; Rare:78 | ||||
| chr9:693561-693752 | Rare:52 | ||||
| chr9:738046-738435 | Common:5; Rare:156; Clinvar:1 | ||||
| chr9:14317006-14317107 | Rare:19 | ||||
| chr9:16726911-16726934 | Rare:7 | ||||
| chr9:17906467-17906861 | Common:1; Rare:140 | ||||
| chr9:17907194-17907429 | Rare:59 |