Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:217631001-217631371 | Common:2; Rare:104 | ||||
chr1:218346145-218346424 | Rare:46; Clinvar (benign):2 | ||||
chr1:219173518-219173938 | Common:1; Rare:139 | ||||
chr1:220272341-220272576 | Rare:64; Clinvar:5 | ||||
chr1:222589871-222589934 | Common:2; Rare:19 | ||||
chr1:222644066-222644407 | Common:3; Rare:100 | ||||
chr1:222712422-222712866 | Common:3; Rare:153 | ||||
chr1:222713243-222713408 | Common:1; Rare:50 | ||||
chr1:224183153-224183361 | Common:2; Rare:88 | ||||
chr1:224616175-224616515 | Common:3; Rare:90 | ||||
chr1:225427987-225428280 | Common:3; Rare:94; Clinvar:3; Clinvar (benign):2 | ||||
chr1:225777737-225777934 | Common:3; Rare:66 | ||||
chr1:225999316-225999616 | Common:2; Rare:100 | ||||
chr1:226062066-226062094 | Rare:6 | ||||
chr1:226062462-226062801 | Rare:123 |