Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231528557-231528750 | Common:2; Rare:71 | ||||
chr1:234373392-234373835 | Common:2; Rare:194; Clinvar (benign):9 | ||||
chr1:235128674-235128964 | Rare:122 | ||||
chr1:235328241-235328636 | Common:2; Rare:116 | ||||
chr1:235504385-235504738 | Common:5; Rare:114 | ||||
chr1:236524524-236524608 | Common:1; Rare:18 | ||||
chr1:236795065-236795410 | Common:6; Rare:142; Clinvar:3 | ||||
chr1:241848100-241848236 | Common:2; Rare:30 | ||||
chr1:243255041-243255433 | Common:1; Rare:95 | ||||
chr1:243255741-243256188 | Common:1; Rare:135; Clinvar:5; Clinvar (benign):1 | ||||
chr1:244863746-244864128 | Common:1; Rare:124; Clinvar:6; Clinvar (benign):6 | ||||
chr1:244864149-244864327 | Rare:47; Clinvar:1; Clinvar (benign):3 | ||||
chr1:246566141-246566594 | Common:3; Rare:152 | ||||
chr1:247331208-247331327 | Rare:38 | ||||
chr1:247331825-247332056 | Rare:63 |