| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89638434-89638538 | Common:1; Rare:23 | ||||
| chr6:89638721-89638845 | Common:3; Rare:42 | ||||
| chr6:89819673-89819917 | Rare:78 | ||||
| chr6:89829595-89829962 | Rare:98 | ||||
| chr6:90586986-90587334 | Common:3; Rare:95 | ||||
| chr6:93419552-93419802 | Common:1; Rare:67 | ||||
| chr6:95577357-95577591 | Common:6; Rare:65 | ||||
| chr6:96521674-96521892 | Common:8; Rare:106 | ||||
| chr6:96897803-96898042 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:98947843-98948255 | Rare:107 | ||||
| chr6:99424865-99424967 | Rare:39 | ||||
| chr6:99425245-99425515 | Common:2; Rare:75 | ||||
| chr6:99425659-99425760 | Rare:24 | ||||
| chr6:99515395-99515489 | Rare:35 | ||||
| chr6:100881084-100881482 | Common:7; Rare:130 |