| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:87589946-87590169 | Common:3; Rare:104; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87702228-87702481 | Common:1; Rare:75 | ||||
| chr6:88963585-88963830 | Common:2; Rare:83 | ||||
| chr6:89117937-89118103 | Common:2; Rare:73 | ||||
| chr6:89638724-89638837 | Common:3; Rare:37 | ||||
| chr6:89819720-89819868 | Rare:53 | ||||
| chr6:89829595-89829949 | Rare:93 | ||||
| chr6:90587018-90587449 | Common:5; Rare:113 | ||||
| chr6:93419538-93419837 | Common:1; Rare:81 | ||||
| chr6:96837417-96837706 | Common:6; Rare:94 | ||||
| chr6:96897817-96898086 | Common:4; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:96924347-96924683 | Common:4; Rare:92 | ||||
| chr6:97283135-97283413 | Common:3; Rare:81 | ||||
| chr6:99425219-99425486 | Common:2; Rare:80 | ||||
| chr6:100881201-100881495 | Common:5; Rare:108 |