Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244451813-244452027 | Rare:67 | ||||
chr1:244835575-244835729 | Common:2; Rare:67; Clinvar (benign):4 | ||||
chr1:244856455-244856857 | Common:1; Rare:80; Clinvar (benign):2 | ||||
chr1:244864056-244864665 | Rare:206; Clinvar:2; Clinvar (benign):3 | ||||
chr1:244969955-244969988 | Rare:7 | ||||
chr1:244969999-244970421 | Common:5; Rare:175 | ||||
chr1:246566209-246566599 | Common:2; Rare:126 | ||||
chr1:247104314-247104561 | Common:2; Rare:74 | ||||
chr1:248838040-248838347 | Common:1; Rare:102 | ||||
chr10:649942-650077 | Common:1; Rare:29 | ||||
chr10:931680-931994 | Rare:102 | ||||
chr10:988325-988470 | Rare:57 | ||||
chr10:1048871-1049086 | Common:2; Rare:114 | ||||
chr10:1056702-1056860 | Common:3; Rare:61 | ||||
chr10:3785120-3785554 | Common:4; Rare:166 |