Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:184974302-184974678 | Rare:103 | ||||
chr1:185045277-185045637 | Common:2; Rare:121 | ||||
chr1:185156690-185156730 | Rare:19 | ||||
chr1:185156733-185157303 | Common:3; Rare:162 | ||||
chr1:185157422-185157533 | Common:1; Rare:37 | ||||
chr1:185316757-185316871 | Rare:30 | ||||
chr1:185317186-185317453 | Common:1; Rare:79 | ||||
chr1:186375087-186375936 | Common:1; Rare:238 | ||||
chr1:190475454-190475732 | Common:1; Rare:67 | ||||
chr1:190478003-190478334 | Rare:83 | ||||
chr1:192808746-192809070 | Common:4; Rare:128 | ||||
chr1:193059264-193059705 | Rare:212 | ||||
chr1:193105384-193105533 | Common:2; Rare:61 | ||||
chr1:193121743-193122194 | Common:2; Rare:163; Clinvar:5; Clinvar (benign):3 | ||||
chr1:193186544-193186698 | Rare:26 |