| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132512663-132512890 | Common:2; Rare:57 | ||||
| chr6:132734762-132734912 | Rare:26 | ||||
| chr6:132814270-132814625 | Common:4; Rare:132 | ||||
| chr6:133889001-133889170 | Common:1; Rare:29 | ||||
| chr6:133953044-133953264 | Common:2; Rare:72 | ||||
| chr6:134174732-134175059 | Common:1; Rare:167 | ||||
| chr6:134175648-134175999 | Common:2; Rare:87 | ||||
| chr6:135497604-135497802 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289756-136290014 | Common:1; Rare:111 | ||||
| chr6:136550361-136550709 | Common:2; Rare:104 | ||||
| chr6:137044700-137044756 | Rare:8 | ||||
| chr6:137219111-137219192 | Rare:20 | ||||
| chr6:137219248-137219518 | Common:4; Rare:96; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:137866941-137867285 | Rare:81 | ||||
| chr6:138107125-138107485 | Common:2; Rare:117 |