Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:139029026-139029191 | Common:5; Rare:43 | ||||
chr6:139374498-139374806 | Common:1; Rare:124 | ||||
chr6:142147140-142147294 | Rare:58 | ||||
chr6:143060618-143060686 | Common:2; Rare:23 | ||||
chr6:143060724-143060926 | Common:7; Rare:71 | ||||
chr6:143450660-143450999 | Common:1; Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
chr6:143843171-143843409 | Common:2; Rare:78 | ||||
chr6:144008247-144008506 | Rare:91 | ||||
chr6:144095477-144095831 | Common:6; Rare:105 | ||||
chr6:144285248-144285378 | Common:2; Rare:31 | ||||
chr6:144582980-144583190 | Rare:35 | ||||
chr6:144583224-144583525 | Common:1; Rare:52 | ||||
chr6:145734781-145734897 | Common:3; Rare:42 | ||||
chr6:145735987-145736049 | Rare:10 | ||||
chr6:145814690-145815118 | Common:2; Rare:171 |