| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:91040786-91041074 | Common:3; Rare:83 | ||||
| chr8:91069979-91070382 | Common:1; Rare:143 | ||||
| chr8:92095212-92095345 | Rare:36 | ||||
| chr8:92966071-92966229 | Common:1; Rare:36 | ||||
| chr8:93700426-93700665 | Common:1; Rare:92 | ||||
| chr8:93916637-93916993 | Common:4; Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:94262313-94262456 | Rare:36 | ||||
| chr8:94436916-94437085 | Rare:36 | ||||
| chr8:94475052-94475203 | Common:3; Rare:41 | ||||
| chr8:94553440-94553763 | Common:3; Rare:115 | ||||
| chr8:94719780-94719983 | Common:1; Rare:63 | ||||
| chr8:94895194-94895329 | Rare:46 | ||||
| chr8:94895626-94895822 | Common:1; Rare:53 | ||||
| chr8:95024905-95025164 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95133597-95133934 | Common:3; Rare:109 |