| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132734758-132734956 | Rare:35 | ||||
| chr6:133888958-133889200 | Common:1; Rare:40 | ||||
| chr6:133889323-133889614 | Common:4; Rare:97; Clinvar:1 | ||||
| chr6:134174822-134175059 | Common:1; Rare:128 | ||||
| chr6:135054785-135054962 | Common:6; Rare:52 | ||||
| chr6:135497604-135497834 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136550401-136550687 | Common:2; Rare:80 | ||||
| chr6:137219113-137219189 | Rare:19 | ||||
| chr6:137219319-137219537 | Common:4; Rare:80; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138572518-138572723 | Common:1; Rare:45 | ||||
| chr6:138773646-138773813 | Common:3; Rare:77 | ||||
| chr6:138795960-138796105 | Common:1; Rare:31 | ||||
| chr6:139028442-139028846 | Common:2; Rare:79 | ||||
| chr6:142147140-142147290 | Rare:56 | ||||
| chr6:142301853-142302138 | Common:6; Rare:85 |