| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:145052198-145052504 | Common:10; Rare:87 | ||||
| chr9:214635-214879 | Common:5; Rare:144; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:215065-215220 | Common:3; Rare:88; Clinvar (benign):1 | ||||
| chr9:504402-504742 | Common:4; Rare:165 | ||||
| chr9:841462-841697 | Common:1; Rare:68 | ||||
| chr9:2015040-2015380 | Common:3; Rare:100 | ||||
| chr9:2017679-2017725 | Rare:14 | ||||
| chr9:2844036-2844349 | Common:5; Rare:120 | ||||
| chr9:3525972-3526087 | Common:1; Rare:40 | ||||
| chr9:3526366-3526526 | Common:5; Rare:83 | ||||
| chr9:4490209-4490222 | Rare:3 | ||||
| chr9:4662178-4662348 | Common:3; Rare:66 | ||||
| chr9:4679423-4679775 | Common:1; Rare:154 | ||||
| chr9:4741083-4741373 | Common:4; Rare:136 | ||||
| chr9:4792779-4793050 | Common:2; Rare:104 |