| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132512644-132512890 | Common:2; Rare:61 | ||||
| chr6:132513006-132513231 | Common:1; Rare:55 | ||||
| chr6:132798765-132799034 | Common:1; Rare:41 | ||||
| chr6:132814270-132814781 | Common:7; Rare:213 | ||||
| chr6:133240507-133240661 | Common:1; Rare:29 | ||||
| chr6:133240805-133240910 | Rare:15 | ||||
| chr6:133240984-133241451 | Common:5; Rare:138 | ||||
| chr6:133953047-133953255 | Common:2; Rare:67 | ||||
| chr6:134174712-134175025 | Common:1; Rare:154 | ||||
| chr6:134175648-134175759 | Rare:40 | ||||
| chr6:134177714-134178091 | Common:1; Rare:78 | ||||
| chr6:134178359-134178409 | Rare:10 | ||||
| chr6:135054773-135055007 | Common:6; Rare:69 | ||||
| chr6:135497604-135497952 | Common:4; Rare:130; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136250272-136250543 | Common:2; Rare:81 |