| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219113-137219229 | Common:1; Rare:40; Clinvar:1 | ||||
| chr6:137219284-137219527 | Common:4; Rare:87; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:137866719-137866773 | Rare:12 | ||||
| chr6:137866959-137867423 | Rare:107 | ||||
| chr6:138773646-138773831 | Common:3; Rare:86 | ||||
| chr6:139028616-139028836 | Common:1; Rare:47 | ||||
| chr6:139291979-139292051 | Rare:8 | ||||
| chr6:139374411-139374491 | Common:2; Rare:27 | ||||
| chr6:139374494-139374807 | Common:1; Rare:126 | ||||
| chr6:142147140-142147290 | Rare:56 | ||||
| chr6:143060663-143060697 | Common:2; Rare:16 | ||||
| chr6:143060707-143060928 | Common:7; Rare:76 | ||||
| chr6:143450642-143450950 | Common:1; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843179-143843465 | Common:2; Rare:95 | ||||
| chr6:144150372-144150537 | Common:4; Rare:51 |