| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:131573009-131573232 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:131628172-131628447 | Common:2; Rare:73 | ||||
| chr6:131951354-131951528 | Common:1; Rare:38 | ||||
| chr6:133953023-133953277 | Common:2; Rare:79 | ||||
| chr6:134174841-134175105 | Common:1; Rare:124 | ||||
| chr6:135497603-135497874 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289756-136290054 | Common:2; Rare:128 | ||||
| chr6:136550385-136550687 | Common:2; Rare:89 | ||||
| chr6:137219284-137219527 | Common:4; Rare:87; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:138773646-138773809 | Common:3; Rare:75 | ||||
| chr6:142147094-142147284 | Common:3; Rare:65 | ||||
| chr6:143060724-143060919 | Common:7; Rare:67 | ||||
| chr6:143450660-143450956 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511659-143511855 | Common:4; Rare:45 | ||||
| chr6:143843232-143843398 | Common:2; Rare:52 |