Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:229271020-229271293 | Rare:91 | ||||
chr1:229508293-229508439 | Common:1; Rare:57 | ||||
chr1:231241141-231241331 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
chr1:231528607-231528729 | Common:1; Rare:51 | ||||
chr1:234373398-234373525 | Common:1; Rare:59; Clinvar (benign):2 | ||||
chr1:234373645-234373775 | Rare:49; Clinvar (benign):3 | ||||
chr1:235128801-235128991 | Rare:74 | ||||
chr1:236065037-236065228 | Rare:81; Clinvar (pathogenic):1 | ||||
chr1:236795086-236795448 | Common:5; Rare:149; Clinvar:3 | ||||
chr1:243255227-243255280 | Common:1; Rare:16 | ||||
chr1:243255776-243256104 | Rare:89; Clinvar:4 | ||||
chr1:244451865-244452214 | Common:1; Rare:117 | ||||
chr1:244864391-244864786 | Common:1; Rare:167 | ||||
chr1:246566176-246566576 | Common:1; Rare:133 | ||||
chr10:988279-988477 | Common:2; Rare:77 |