| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136250272-136250506 | Common:2; Rare:70 | ||||
| chr6:136289774-136290081 | Common:2; Rare:137 | ||||
| chr6:136550394-136550687 | Common:2; Rare:84 | ||||
| chr6:137219319-137219509 | Common:4; Rare:66; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138107118-138107237 | Rare:38 | ||||
| chr6:138107245-138107681 | Common:5; Rare:131 | ||||
| chr6:138773646-138773813 | Common:3; Rare:77 | ||||
| chr6:139028628-139028842 | Common:1; Rare:44 | ||||
| chr6:139029041-139029146 | Common:4; Rare:24 | ||||
| chr6:142147128-142147300 | Common:1; Rare:65 | ||||
| chr6:142301858-142302161 | Common:6; Rare:89 | ||||
| chr6:142302395-142302703 | Common:1; Rare:62 | ||||
| chr6:143060391-143060488 | Rare:23 | ||||
| chr6:143060724-143060946 | Common:7; Rare:80 | ||||
| chr6:143450642-143450936 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):1 |