| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89819768-89819863 | Rare:28 | ||||
| chr6:89829614-89829909 | Rare:69 | ||||
| chr6:90587018-90587202 | Common:2; Rare:59 | ||||
| chr6:95577424-95577567 | Common:3; Rare:40 | ||||
| chr6:96521674-96521871 | Common:8; Rare:95 | ||||
| chr6:96897797-96898031 | Common:4; Rare:88; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:97283170-97283302 | Common:1; Rare:48 | ||||
| chr6:99425245-99425626 | Common:2; Rare:93 | ||||
| chr6:99515395-99515585 | Common:1; Rare:63 | ||||
| chr6:100881189-100881517 | Common:6; Rare:117 | ||||
| chr6:106325594-106325892 | Common:1; Rare:106 | ||||
| chr6:106629462-106629649 | Common:3; Rare:44 | ||||
| chr6:107459456-107459743 | Common:2; Rare:73; Clinvar:1 | ||||
| chr6:108260764-108260847 | Rare:23 | ||||
| chr6:108294802-108295103 | Common:1; Rare:84 |