| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133953044-133953306 | Common:2; Rare:84 | ||||
| chr6:134174803-134175032 | Common:1; Rare:127 | ||||
| chr6:135054785-135054916 | Common:3; Rare:38 | ||||
| chr6:135497618-135497897 | Common:4; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289756-136289860 | Rare:41 | ||||
| chr6:136550379-136550691 | Common:2; Rare:94 | ||||
| chr6:137219289-137219463 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138773646-138773836 | Common:3; Rare:88 | ||||
| chr6:142147140-142147300 | Rare:63 | ||||
| chr6:142301853-142302018 | Common:3; Rare:48 | ||||
| chr6:143060700-143060919 | Common:7; Rare:73 | ||||
| chr6:143450660-143450941 | Common:1; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511655-143511952 | Common:4; Rare:63 | ||||
| chr6:143843196-143843398 | Common:2; Rare:64 | ||||
| chr6:144285171-144285501 | Common:3; Rare:88 |