| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:131063142-131063474 | Rare:97 | ||||
| chr6:131250378-131250574 | Common:1; Rare:50 | ||||
| chr6:131628108-131628463 | Common:3; Rare:93 | ||||
| chr6:131951368-131951625 | Common:2; Rare:51 | ||||
| chr6:132401177-132401663 | Common:3; Rare:145 | ||||
| chr6:132798560-132798673 | Common:3; Rare:22 | ||||
| chr6:133888998-133889217 | Common:1; Rare:38 | ||||
| chr6:133953047-133953291 | Common:2; Rare:80 | ||||
| chr6:134174710-134175128 | Common:1; Rare:197 | ||||
| chr6:134175648-134175765 | Rare:41 | ||||
| chr6:134175770-134176134 | Common:2; Rare:64 | ||||
| chr6:134177843-134178091 | Common:1; Rare:37 | ||||
| chr6:135054784-135054973 | Common:6; Rare:54 | ||||
| chr6:135497603-135497973 | Common:4; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289223-136289452 | Rare:88 |