| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:135497604-135497971 | Common:4; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289322-136289467 | Rare:75 | ||||
| chr6:136289767-136290063 | Common:2; Rare:132 | ||||
| chr6:136550395-136550751 | Common:2; Rare:93 | ||||
| chr6:136792543-136792654 | Rare:36 | ||||
| chr6:136793002-136793250 | Common:1; Rare:68 | ||||
| chr6:137219111-137219229 | Common:1; Rare:40; Clinvar:1 | ||||
| chr6:137219262-137219521 | Common:4; Rare:90; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:137219557-137219638 | Common:1; Rare:14; Clinvar:1 | ||||
| chr6:137866939-137867281 | Rare:81 | ||||
| chr6:137870842-137871106 | Common:1; Rare:53 | ||||
| chr6:138107383-138107673 | Common:5; Rare:74 | ||||
| chr6:138404003-138404569 | Common:8; Rare:166 | ||||
| chr6:138545641-138545871 | Common:1; Rare:43 | ||||
| chr6:138773646-138773846 | Common:3; Rare:90 |