Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:32844616-32844840 | Common:1; Rare:48 | ||||
chr6:32853660-32853819 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):3 | ||||
chr6:32853985-32854228 | Common:2; Rare:57 | ||||
chr6:32968801-32968933 | Common:4; Rare:40 | ||||
chr6:32970769-32970952 | Common:1; Rare:49 | ||||
chr6:33200356-33200457 | Rare:26 | ||||
chr6:33200656-33200976 | Common:3; Rare:93 | ||||
chr6:33271632-33272131 | Common:4; Rare:180 | ||||
chr6:33288985-33289106 | Rare:44 | ||||
chr6:33289514-33289644 | Rare:32 | ||||
chr6:33298876-33299022 | Rare:35 | ||||
chr6:33417879-33417959 | Rare:34 | ||||
chr6:33417989-33418455 | Common:2; Rare:116 | ||||
chr6:33454424-33454620 | Rare:50 | ||||
chr6:34236752-34236914 | Common:2; Rare:64 |