| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:131807892-131808023 | Common:4; Rare:39; Clinvar (benign):1 | ||||
| chr6:132513044-132513253 | Common:1; Rare:52 | ||||
| chr6:132798512-132798728 | Common:19; Rare:104 | ||||
| chr6:132814304-132814607 | Common:6; Rare:208 | ||||
| chr6:133240340-133240964 | Common:4; Rare:180 | ||||
| chr6:133241022-133241742 | Common:14; Rare:279; Clinvar:5; Clinvar (benign):3 | ||||
| chr6:133953020-133953304 | Common:4; Rare:151 | ||||
| chr6:134174647-134175142 | Common:2; Rare:417 | ||||
| chr6:134175651-134176016 | Common:4; Rare:160 | ||||
| chr6:134177753-134178100 | Common:2; Rare:122 | ||||
| chr6:134178218-134178527 | Common:2; Rare:104 | ||||
| chr6:135054784-135054992 | Common:12; Rare:122 | ||||
| chr6:135181010-135181410 | Common:4; Rare:216 | ||||
| chr6:135497561-135497912 | Common:8; Rare:199; Clinvar:3; Clinvar (benign):4 | ||||
| chr6:135851481-135851792 | Rare:50 |