Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207751946-207752284 | Common:2; Rare:106; Clinvar:1 | ||||
chr1:209652395-209652571 | Rare:44; Clinvar:1 | ||||
chr1:209675264-209675530 | Common:2; Rare:70 | ||||
chr1:209806002-209806269 | Common:4; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827868-209828066 | Common:1; Rare:54 | ||||
chr1:212035510-212035762 | Common:1; Rare:63 | ||||
chr1:212608478-212608767 | Rare:73 | ||||
chr1:212791714-212791926 | Common:5; Rare:95 | ||||
chr1:212858089-212858273 | Common:3; Rare:47; Clinvar:1 | ||||
chr1:217631020-217631375 | Common:2; Rare:98 | ||||
chr1:219173766-219173905 | Common:1; Rare:75 | ||||
chr1:220046444-220046556 | Rare:39 | ||||
chr1:221742072-221742288 | Rare:59 | ||||
chr1:222589912-222589934 | Rare:4 | ||||
chr1:222712459-222712879 | Common:3; Rare:149 |