| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:117675203-117675477 | Common:3; Rare:70 | ||||
| chr6:119349672-119349909 | Common:2; Rare:75 | ||||
| chr6:125790830-125790992 | Common:2; Rare:59 | ||||
| chr6:127266787-127266975 | Common:1; Rare:77 | ||||
| chr6:127343149-127343645 | Common:3; Rare:123 | ||||
| chr6:136289778-136290054 | Common:2; Rare:119 | ||||
| chr6:138773677-138773809 | Common:3; Rare:66 | ||||
| chr6:143060752-143060921 | Common:6; Rare:61 | ||||
| chr6:143450624-143450937 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843222-143843460 | Common:2; Rare:78 | ||||
| chr6:144008228-144008625 | Common:2; Rare:132 | ||||
| chr6:144285149-144285339 | Common:2; Rare:59 | ||||
| chr6:145814696-145814917 | Common:1; Rare:106 | ||||
| chr6:149896086-149896181 | Rare:16 | ||||
| chr6:151452034-151452538 | Common:4; Rare:176 |