| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:131063155-131063491 | Rare:99 | ||||
| chr6:131628113-131628416 | Common:3; Rare:86 | ||||
| chr6:131951370-131951642 | Common:2; Rare:56 | ||||
| chr6:132401452-132401579 | Common:1; Rare:36 | ||||
| chr6:132734724-132734908 | Common:1; Rare:35 | ||||
| chr6:132814318-132814612 | Common:3; Rare:112 | ||||
| chr6:133953040-133953246 | Common:2; Rare:62 | ||||
| chr6:134174847-134175121 | Common:1; Rare:123 | ||||
| chr6:134177843-134178040 | Rare:32 | ||||
| chr6:135054784-135055016 | Common:6; Rare:68 | ||||
| chr6:135497603-135497856 | Common:4; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289756-136290014 | Common:1; Rare:111 | ||||
| chr6:136550361-136550695 | Common:2; Rare:101 | ||||
| chr6:137219092-137219204 | Common:1; Rare:31 | ||||
| chr6:137219291-137219511 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |