| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:87589955-87590169 | Common:3; Rare:97; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702203-87702445 | Common:1; Rare:77 | ||||
| chr6:88963585-88963830 | Common:2; Rare:83 | ||||
| chr6:89080600-89080764 | Common:1; Rare:74 | ||||
| chr6:89638434-89638532 | Common:1; Rare:18 | ||||
| chr6:89638712-89638806 | Common:3; Rare:35 | ||||
| chr6:89819726-89819903 | Rare:62 | ||||
| chr6:89829614-89829949 | Rare:86 | ||||
| chr6:93419546-93419824 | Common:1; Rare:75 | ||||
| chr6:95577409-95577614 | Common:5; Rare:58 | ||||
| chr6:96521674-96521876 | Common:8; Rare:98 | ||||
| chr6:96897821-96898086 | Common:4; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283149-97283401 | Common:3; Rare:74 | ||||
| chr6:99424684-99424927 | Rare:64 | ||||
| chr6:99425253-99425496 | Common:2; Rare:68 |