| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219113-137219260 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:137219274-137219497 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:138773579-138773836 | Common:3; Rare:106 | ||||
| chr6:142147116-142147289 | Common:3; Rare:62 | ||||
| chr6:142301846-142302135 | Common:6; Rare:84 | ||||
| chr6:143060724-143060935 | Common:7; Rare:76 | ||||
| chr6:143450667-143450961 | Common:1; Rare:108; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511655-143511863 | Common:4; Rare:49 | ||||
| chr6:144150236-144150529 | Common:5; Rare:82 | ||||
| chr6:145814664-145814927 | Common:1; Rare:118 | ||||
| chr6:145964291-145964553 | Common:1; Rare:90 | ||||
| chr6:149746480-149746627 | Common:2; Rare:69 | ||||
| chr6:149749617-149749796 | Rare:98 | ||||
| chr6:151452062-151452548 | Common:4; Rare:174 | ||||
| chr6:153002582-153002861 | Common:4; Rare:103 |