| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133953040-133953233 | Common:2; Rare:58 | ||||
| chr6:134174731-134174989 | Common:1; Rare:128 | ||||
| chr6:134177843-134178051 | Rare:32 | ||||
| chr6:135054763-135054990 | Common:6; Rare:70 | ||||
| chr6:135497604-135497834 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289767-136290063 | Common:2; Rare:132 | ||||
| chr6:136550346-136550669 | Common:2; Rare:100 | ||||
| chr6:137044658-137044754 | Rare:23 | ||||
| chr6:137044890-137045078 | Common:2; Rare:46 | ||||
| chr6:137219113-137219228 | Common:1; Rare:39; Clinvar:1 | ||||
| chr6:137219274-137219493 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:137866931-137867285 | Rare:81 | ||||
| chr6:137867486-137867489 | Rare:1 | ||||
| chr6:137867758-137867984 | Rare:44 | ||||
| chr6:138107029-138107572 | Common:5; Rare:175 |