| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:129710045-129710324 | Common:1; Rare:87 | ||||
| chr6:129710338-129710395 | Common:1; Rare:18 | ||||
| chr6:131013584-131013702 | Common:1; Rare:21 | ||||
| chr6:131063148-131063564 | Rare:119 | ||||
| chr6:131573141-131573239 | Common:1; Rare:17; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:131628051-131628461 | Common:3; Rare:111 | ||||
| chr6:132814276-132814611 | Common:3; Rare:122 | ||||
| chr6:132814729-132815114 | Common:5; Rare:180 | ||||
| chr6:133889002-133889203 | Common:1; Rare:35 | ||||
| chr6:133953026-133953278 | Common:2; Rare:79 | ||||
| chr6:134174475-134174665 | Rare:81 | ||||
| chr6:134174710-134175036 | Common:1; Rare:162 | ||||
| chr6:134175566-134175802 | Rare:82 | ||||
| chr6:134177810-134178091 | Common:1; Rare:50 | ||||
| chr6:135054784-135054973 | Common:6; Rare:54 |