Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23369935-23370280 | Rare:73 | ||||
chr1:23484176-23484515 | Common:1; Rare:98 | ||||
chr1:23484520-23484910 | Common:7; Rare:76 | ||||
chr1:23531184-23531517 | Common:3; Rare:50 | ||||
chr1:23558490-23558686 | Common:1; Rare:69 | ||||
chr1:23559423-23559704 | Common:2; Rare:116 | ||||
chr1:23691669-23691836 | Common:3; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
chr1:23743295-23743526 | Rare:86 | ||||
chr1:23743738-23744564 | Common:3; Rare:300 | ||||
chr1:23778227-23778452 | Common:6; Rare:110 | ||||
chr1:23791010-23791221 | Rare:67 | ||||
chr1:23800698-23800974 | Common:1; Rare:97 | ||||
chr1:23825334-23825599 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:23958984-23959234 | Common:3; Rare:42 | ||||
chr1:23959607-23959854 | Common:2; Rare:66 |