| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137866959-137867237 | Rare:62 | ||||
| chr6:138107474-138107617 | Common:4; Rare:39 | ||||
| chr6:138403993-138404254 | Common:2; Rare:79 | ||||
| chr6:138773701-138773879 | Common:3; Rare:82 | ||||
| chr6:139028367-139028872 | Common:2; Rare:99 | ||||
| chr6:139028948-139029180 | Common:8; Rare:69 | ||||
| chr6:139374193-139374663 | Common:4; Rare:187 | ||||
| chr6:142147163-142147376 | Rare:97 | ||||
| chr6:142301830-142302143 | Common:6; Rare:91 | ||||
| chr6:142944479-142944726 | Rare:57 | ||||
| chr6:142945161-142945456 | Common:1; Rare:68 | ||||
| chr6:143060731-143061057 | Common:8; Rare:114 | ||||
| chr6:143450592-143450956 | Common:1; Rare:133; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511658-143512013 | Common:5; Rare:75 | ||||
| chr6:143677794-143678106 | Common:2; Rare:75 |