| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89638439-89638845 | Common:6; Rare:124 | ||||
| chr6:89672662-89672795 | Rare:30 | ||||
| chr6:89829595-89829962 | Rare:98 | ||||
| chr6:93419557-93419821 | Common:1; Rare:71 | ||||
| chr6:95577359-95577571 | Common:5; Rare:57 | ||||
| chr6:96521687-96521879 | Common:6; Rare:90 | ||||
| chr6:96897827-96898044 | Common:4; Rare:75; Clinvar:3 | ||||
| chr6:99424706-99424963 | Rare:76 | ||||
| chr6:99425219-99425494 | Common:2; Rare:81 | ||||
| chr6:100881189-100881485 | Common:6; Rare:107 | ||||
| chr6:105137105-105137257 | Common:1; Rare:59 | ||||
| chr6:106629457-106629623 | Common:1; Rare:35 | ||||
| chr6:107459551-107459877 | Common:3; Rare:72 | ||||
| chr6:108074600-108074871 | Common:1; Rare:95; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:108260796-108261296 | Common:2; Rare:194 |