Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193105062-193105860 | Common:26; Rare:1090 | ||||
chr1:193121430-193122297 | Common:22; Rare:1395; Clinvar:35; Clinvar (benign):33; Clinvar (pathogenic):8 | ||||
chr1:193122209-193122710 | Rare:477; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:196608420-196609080 | Common:2; Rare:404 | ||||
chr1:196651883-196652288 | Common:6; Rare:184; Clinvar:6; Clinvar (benign):12 | ||||
chr1:197146151-197146270 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
chr1:197146174-197146957 | Common:2; Rare:562; Clinvar:22; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr1:197200289-197200886 | Common:9; Rare:235 | ||||
chr1:197774420-197775590 | Common:9; Rare:808 | ||||
chr1:197775850-197776250 | Common:1; Rare:86 | ||||
chr1:197901927-197902327 | Common:2; Rare:73 | ||||
chr1:197902457-197902673 | Common:1; Rare:137 | ||||
chr1:197902666-197903210 | Common:11; Rare:773 | ||||
chr1:198156780-198157865 | Common:20; Rare:1148 | ||||
chr1:198638757-198639302 | Common:14; Rare:154 |