| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44387407-44387753 | Common:4; Rare:87 | ||||
| chr6:46129805-46129964 | Common:3; Rare:37 | ||||
| chr6:46652718-46653022 | Rare:75 | ||||
| chr6:47477704-47478006 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:49463166-49463397 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52671039-52671167 | Rare:38 | ||||
| chr6:52995267-52995812 | Common:4; Rare:227 | ||||
| chr6:53065385-53065601 | Common:1; Rare:67 | ||||
| chr6:53665656-53665929 | Common:1; Rare:58 | ||||
| chr6:54846574-54846820 | Common:1; Rare:61 | ||||
| chr6:70413176-70413464 | Common:2; Rare:83 | ||||
| chr6:73518352-73519187 | Common:1; Rare:254 | ||||
| chr6:73653956-73654163 | Common:3; Rare:58; Clinvar:2 | ||||
| chr6:73695984-73696218 | Common:1; Rare:46 | ||||
| chr6:75205881-75206270 | Common:2; Rare:95 |