| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132401245-132401632 | Common:3; Rare:115 | ||||
| chr6:132513011-132513240 | Common:1; Rare:57 | ||||
| chr6:132798568-132798728 | Common:9; Rare:46 | ||||
| chr6:133888958-133889170 | Common:1; Rare:35 | ||||
| chr6:133889305-133889604 | Common:4; Rare:100; Clinvar:1 | ||||
| chr6:133889724-133889785 | Rare:11 | ||||
| chr6:133953020-133953304 | Common:2; Rare:88 | ||||
| chr6:134174847-134175017 | Common:1; Rare:78 | ||||
| chr6:135497604-135497860 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289737-136290014 | Common:1; Rare:119 | ||||
| chr6:136550395-136550695 | Common:2; Rare:87 | ||||
| chr6:137219113-137219223 | Common:1; Rare:36 | ||||
| chr6:137219317-137219463 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138773646-138773855 | Common:3; Rare:93 | ||||
| chr6:139028641-139028842 | Common:1; Rare:43 |