| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97922173-97922349 | Common:1; Rare:62 | ||||
| chr9:97922463-97922673 | Common:4; Rare:99 | ||||
| chr9:98056550-98056732 | Common:1; Rare:56 | ||||
| chr9:98119181-98119274 | Common:1; Rare:26 | ||||
| chr9:98255563-98255904 | Common:3; Rare:105 | ||||
| chr9:99221976-99222301 | Common:2; Rare:106 | ||||
| chr9:99821628-99822008 | Rare:113 | ||||
| chr9:100098948-100099220 | Common:2; Rare:77 | ||||
| chr9:100352911-100352978 | Rare:21 | ||||
| chr9:101398585-101398917 | Common:1; Rare:107 | ||||
| chr9:104747476-104747767 | Rare:72 | ||||
| chr9:107283348-107283650 | Common:3; Rare:66 | ||||
| chr9:107488326-107488561 | Common:1; Rare:62 | ||||
| chr9:108934040-108934477 | Common:7; Rare:171; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:111631204-111631369 | Common:1; Rare:51 |