| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:128883002-128883224 | Common:2; Rare:49; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:129710160-129710346 | Rare:44 | ||||
| chr6:131063148-131063432 | Rare:80 | ||||
| chr6:131135488-131135758 | Common:4; Rare:118 | ||||
| chr6:131628101-131628433 | Common:3; Rare:89 | ||||
| chr6:132401422-132401609 | Common:1; Rare:55 | ||||
| chr6:132814276-132814781 | Common:6; Rare:213 | ||||
| chr6:133889002-133889160 | Common:1; Rare:27 | ||||
| chr6:134174859-134175053 | Common:1; Rare:93 | ||||
| chr6:135054769-135054990 | Common:6; Rare:69 | ||||
| chr6:135497588-135497897 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136289316-136289457 | Rare:71 | ||||
| chr6:136289747-136290063 | Common:2; Rare:141 | ||||
| chr6:137219111-137219153 | Rare:11 | ||||
| chr6:137219323-137219490 | Common:2; Rare:57; Clinvar (benign):2; Clinvar (pathogenic):1 |