Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:89083488-89083789 | Common:2; Rare:79 | ||||
chr6:108562699-108562743 | Common:1; Rare:15 | ||||
chr6:108589204-108589672 | Common:1; Rare:94 | ||||
chr6:108654085-108654351 | Common:3; Rare:44 | ||||
chr6:110876307-110876412 | Common:1; Rare:25 | ||||
chr6:111552383-111552610 | Common:2; Rare:46 | ||||
chr6:111559713-111559889 | Rare:33 | ||||
chr6:111694441-111694709 | Common:2; Rare:58 | ||||
chr6:117999195-117999323 | Common:3; Rare:33 | ||||
chr6:121437489-121437578 | Common:1; Rare:19 | ||||
chr6:129130435-129130455 | Rare:7 | ||||
chr6:129315545-129315852 | Rare:83; Clinvar:7; Clinvar (pathogenic):4 | ||||
chr6:129505090-129505322 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr6:132817022-132817158 | Common:1; Rare:46 | ||||
chr6:133891688-133891742 | Rare:17 |