Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236604469-236604626 | Common:4; Rare:47 | ||||
chr1:236795086-236795453 | Common:5; Rare:153; Clinvar:3 | ||||
chr1:241519682-241519985 | Common:2; Rare:89; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:241848129-241848232 | Rare:19 | ||||
chr1:243255040-243255422 | Common:1; Rare:89 | ||||
chr1:243255741-243256182 | Common:1; Rare:130; Clinvar:5; Clinvar (benign):1 | ||||
chr1:244864140-244864182 | Rare:14; Clinvar (benign):1 | ||||
chr1:244864185-244864677 | Rare:166; Clinvar:1; Clinvar (benign):1 | ||||
chr1:246566165-246566563 | Common:2; Rare:134 | ||||
chr1:247078760-247078917 | Rare:40 | ||||
chr1:247172007-247172045 | Common:1; Rare:6 | ||||
chr1:248838038-248838373 | Common:2; Rare:107 | ||||
chr1:248858941-248859195 | Rare:99 | ||||
chr1:248906115-248906312 | Common:1; Rare:86 | ||||
chr10:988314-988507 | Common:1; Rare:82 |