Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207321444-207321742 | Common:1; Rare:76 | ||||
chr1:207751933-207752259 | Common:2; Rare:106; Clinvar:1 | ||||
chr1:209675265-209675472 | Common:1; Rare:50 | ||||
chr1:209784502-209784740 | Common:1; Rare:83 | ||||
chr1:209937987-209938267 | Common:3; Rare:98; Clinvar (pathogenic):1 | ||||
chr1:211675476-211675746 | Rare:58 | ||||
chr1:212035498-212035793 | Common:2; Rare:78 | ||||
chr1:212414788-212415019 | Common:3; Rare:81 | ||||
chr1:212608495-212608761 | Rare:66 | ||||
chr1:212791714-212791930 | Common:5; Rare:97 | ||||
chr1:212858057-212858308 | Common:5; Rare:68; Clinvar:2 | ||||
chr1:212950312-212950610 | Common:2; Rare:70 | ||||
chr1:213015697-213015915 | Rare:60 | ||||
chr1:217631015-217631385 | Common:3; Rare:107 | ||||
chr1:218285212-218285452 | Common:3; Rare:99 |