Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19312080-19312352 | Common:6; Rare:127 | ||||
chr1:19596869-19597064 | Common:2; Rare:91 | ||||
chr1:20661340-20661707 | Common:3; Rare:132; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786591-20786861 | Rare:102 | ||||
chr1:20787196-20787460 | Rare:125 | ||||
chr1:21345463-21345648 | Common:2; Rare:72 | ||||
chr1:21551122-21551279 | Rare:32 | ||||
chr1:21782915-21783272 | Common:2; Rare:118 | ||||
chr1:23019328-23019501 | Rare:50 | ||||
chr1:23368207-23368513 | Common:1; Rare:87 | ||||
chr1:23559434-23559643 | Common:1; Rare:92 | ||||
chr1:23800745-23800959 | Common:1; Rare:73 | ||||
chr1:23825405-23825572 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23980237-23980497 | Rare:78 | ||||
chr1:24502238-24502386 | Common:1; Rare:44 |