Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236604464-236604659 | Common:4; Rare:57 | ||||
chr1:236795086-236795420 | Common:5; Rare:139; Clinvar:3 | ||||
chr1:241519667-241519963 | Common:2; Rare:99; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr1:241848094-241848251 | Common:2; Rare:32 | ||||
chr1:243255047-243255433 | Common:1; Rare:92 | ||||
chr1:243255741-243256140 | Common:1; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451840-244452112 | Common:1; Rare:103 | ||||
chr1:244835602-244835747 | Common:1; Rare:69; Clinvar (benign):5 | ||||
chr1:244863994-244864285 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):5 | ||||
chr1:244864352-244864675 | Rare:120 | ||||
chr1:246566163-246566511 | Common:2; Rare:123 | ||||
chr1:247078765-247078877 | Rare:26 | ||||
chr1:247104334-247104570 | Common:2; Rare:67 | ||||
chr10:135354-135540 | Rare:52 | ||||
chr10:988305-988470 | Rare:61 |