| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:470123-470350 | Common:16; Rare:99 | ||||
| chr9:2015060-2015366 | Common:3; Rare:90 | ||||
| chr9:2181888-2182194 | Common:1; Rare:111; Clinvar:1 | ||||
| chr9:2621288-2621585 | Common:4; Rare:118 | ||||
| chr9:2621848-2622208 | Common:6; Rare:131; Clinvar:9; Clinvar (benign):4 | ||||
| chr9:2622223-2622264 | Rare:20; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:2844047-2844329 | Common:5; Rare:104 | ||||
| chr9:4662188-4662323 | Common:3; Rare:44 | ||||
| chr9:4679423-4679738 | Common:1; Rare:138 | ||||
| chr9:4741091-4741365 | Common:4; Rare:126 | ||||
| chr9:4792674-4793037 | Common:2; Rare:134 | ||||
| chr9:5304157-5304378 | Rare:68 | ||||
| chr9:5437817-5438040 | Common:2; Rare:71 | ||||
| chr9:5628989-5629215 | Common:1; Rare:103 | ||||
| chr9:6015603-6015719 | Rare:50 |