| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:182142447-182142688 | Common:2; Rare:56 | ||||
| chr4:183504243-183504324 | Common:2; Rare:20 | ||||
| chr4:183765676-183765712 | Common:1; Rare:8 | ||||
| chr4:183798105-183798356 | Common:3; Rare:54 | ||||
| chr4:184813487-184813695 | Common:2; Rare:41 | ||||
| chr4:184815058-184815275 | Common:2; Rare:46 | ||||
| chr4:185384866-185385139 | Common:3; Rare:51 | ||||
| chr4:185504474-185504696 | Common:1; Rare:69; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:185817505-185817736 | Common:3; Rare:57 | ||||
| chr5:91953-92214 | Rare:90 | ||||
| chr5:784692-784842 | Common:2; Rare:46 | ||||
| chr5:1633910-1634083 | Common:2; Rare:64 | ||||
| chr5:8457562-8457765 | Common:2; Rare:72 | ||||
| chr5:10702004-10702255 | Rare:44 | ||||
| chr5:10748210-10748538 | Common:1; Rare:61 |