| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132401428-132401622 | Common:1; Rare:57 | ||||
| chr6:132814304-132814611 | Common:3; Rare:116 | ||||
| chr6:133889048-133889194 | Rare:21 | ||||
| chr6:133953040-133953233 | Common:2; Rare:58 | ||||
| chr6:134174857-134175004 | Common:1; Rare:63 | ||||
| chr6:135497604-135497919 | Common:4; Rare:118; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289747-136290017 | Common:1; Rare:117 | ||||
| chr6:136550394-136550682 | Common:2; Rare:84 | ||||
| chr6:137044710-137045033 | Rare:76 | ||||
| chr6:137219129-137219199 | Common:1; Rare:19 | ||||
| chr6:137219310-137219527 | Common:4; Rare:78; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:137866941-137867227 | Rare:65 | ||||
| chr6:138404161-138404564 | Common:7; Rare:110 | ||||
| chr6:138773646-138773865 | Common:3; Rare:97 | ||||
| chr6:139028507-139028819 | Common:1; Rare:62 |