| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125986330-125986736 | Common:1; Rare:265 | ||||
| chr6:126339974-126340253 | Common:1; Rare:83 | ||||
| chr6:127266767-127266916 | Common:4; Rare:126 | ||||
| chr6:127342990-127343190 | Common:5; Rare:76 | ||||
| chr6:127343272-127343660 | Common:3; Rare:155 | ||||
| chr6:128520410-128520770 | Common:5; Rare:216 | ||||
| chr6:129710021-129710417 | Common:6; Rare:216 | ||||
| chr6:130827270-130827599 | Common:9; Rare:196 | ||||
| chr6:131063137-131063464 | Rare:186 | ||||
| chr6:131135330-131135764 | Common:7; Rare:251 | ||||
| chr6:131628020-131628484 | Common:6; Rare:236 | ||||
| chr6:131807884-131808227 | Common:14; Rare:154; Clinvar:4; Clinvar (benign):6 | ||||
| chr6:131951265-131951460 | Rare:105 | ||||
| chr6:132798556-132798778 | Common:9; Rare:51 | ||||
| chr6:132814182-132814856 | Common:13; Rare:404 |