Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373388-234373543 | Common:1; Rare:81; Clinvar (benign):3 | ||||
chr1:234373666-234373768 | Rare:41; Clinvar (benign):2 | ||||
chr1:235866910-235867226 | Common:2; Rare:94 | ||||
chr1:236795054-236795321 | Common:5; Rare:92; Clinvar:1 | ||||
chr1:241848123-241848233 | Common:1; Rare:20 | ||||
chr1:243255191-243255420 | Common:1; Rare:51 | ||||
chr1:243255776-243256113 | Rare:94; Clinvar:4 | ||||
chr1:244451807-244452212 | Common:1; Rare:136 | ||||
chr1:244835588-244835736 | Common:1; Rare:64; Clinvar (benign):4 | ||||
chr1:244864437-244864718 | Common:1; Rare:114 | ||||
chr1:244970211-244970414 | Common:4; Rare:99 | ||||
chr1:246566209-246566591 | Common:2; Rare:123 | ||||
chr10:988310-988468 | Rare:58 | ||||
chr10:1048878-1049099 | Common:2; Rare:112 | ||||
chr10:3067352-3067570 | Common:2; Rare:84 |