| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79078150-79078606 | Common:1; Rare:191 | ||||
| chr6:80106386-80106690 | Common:2; Rare:98 | ||||
| chr6:83193186-83193389 | Common:3; Rare:65 | ||||
| chr6:85449540-85449812 | Common:2; Rare:65 | ||||
| chr6:85449955-85449971 | Rare:3 | ||||
| chr6:85449994-85450445 | Common:1; Rare:139 | ||||
| chr6:85642798-85643066 | Common:3; Rare:96 | ||||
| chr6:87155279-87155618 | Rare:99 | ||||
| chr6:87589950-87590186 | Common:3; Rare:112; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:89819720-89819917 | Rare:66 | ||||
| chr6:95577386-95577597 | Common:6; Rare:59 | ||||
| chr6:96521781-96521866 | Common:3; Rare:44 | ||||
| chr6:96897796-96898047 | Common:4; Rare:92; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:100881265-100881505 | Common:5; Rare:96 | ||||
| chr6:105179961-105180052 | Common:1; Rare:22 |