| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104747608-104747745 | Rare:32 | ||||
| chr9:104928153-104928347 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:105245098-105245261 | Rare:42 | ||||
| chr9:106862431-106862800 | Common:4; Rare:93 | ||||
| chr9:106862973-106863186 | Rare:74 | ||||
| chr9:106863286-106863660 | Common:1; Rare:78 | ||||
| chr9:107282972-107283292 | Common:2; Rare:108 | ||||
| chr9:107284015-107284316 | Common:1; Rare:81 | ||||
| chr9:108933999-108934493 | Common:7; Rare:193; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109013438-109013779 | Common:2; Rare:119 | ||||
| chr9:109498255-109498375 | Rare:40 | ||||
| chr9:110125340-110125509 | Rare:31 | ||||
| chr9:110256414-110256725 | Common:5; Rare:109 | ||||
| chr9:111484138-111484479 | Common:1; Rare:170 | ||||
| chr9:111525082-111525237 | Common:5; Rare:55 |