Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:17054102-17054395 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
chr1:17439649-17439892 | Rare:82 | ||||
chr1:18480832-18481020 | Common:2; Rare:41 | ||||
chr1:19210071-19210515 | Rare:148 | ||||
chr1:19240381-19240680 | Common:2; Rare:67 | ||||
chr1:19251494-19251857 | Common:6; Rare:123 | ||||
chr1:19311877-19312350 | Common:9; Rare:213 | ||||
chr1:19485420-19485737 | Common:1; Rare:103 | ||||
chr1:19596846-19597064 | Common:2; Rare:96 | ||||
chr1:19799670-19800011 | Common:5; Rare:107 | ||||
chr1:20486188-20486407 | Rare:52 | ||||
chr1:20508022-20508229 | Common:2; Rare:71 | ||||
chr1:20661346-20661682 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786564-20786780 | Rare:76 | ||||
chr1:20787196-20787416 | Rare:107 |