| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219319-137219496 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:137866941-137867233 | Rare:66 | ||||
| chr6:138773646-138773813 | Common:3; Rare:77 | ||||
| chr6:139028553-139028826 | Common:1; Rare:54 | ||||
| chr6:142147140-142147304 | Rare:67 | ||||
| chr6:143060724-143060954 | Common:7; Rare:81 | ||||
| chr6:143450667-143450971 | Common:1; Rare:108; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843196-143843409 | Common:2; Rare:69 | ||||
| chr6:144150297-144150529 | Common:5; Rare:65 | ||||
| chr6:144285174-144285372 | Common:3; Rare:60 | ||||
| chr6:144286181-144286546 | Common:4; Rare:72 | ||||
| chr6:145814664-145814927 | Common:1; Rare:118 | ||||
| chr6:148342942-148343089 | Rare:31 | ||||
| chr6:149718059-149718151 | Common:1; Rare:30 | ||||
| chr6:149746496-149746642 | Common:2; Rare:72 |