Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153670926-153671247 | Rare:109 | ||||
chr1:153678531-153678697 | Common:1; Rare:31 | ||||
chr1:153727765-153728082 | Common:1; Rare:96 | ||||
chr1:153945239-153945390 | Rare:22 | ||||
chr1:153963479-153963738 | Common:2; Rare:69 | ||||
chr1:153967623-153967954 | Common:1; Rare:59 | ||||
chr1:153986202-153986418 | Rare:58 | ||||
chr1:153990697-153990901 | Common:2; Rare:106 | ||||
chr1:154182987-154183277 | Rare:93 | ||||
chr1:154220515-154220973 | Common:1; Rare:154 | ||||
chr1:154956089-154956241 | Common:1; Rare:43 | ||||
chr1:154961712-154962029 | Common:1; Rare:110 | ||||
chr1:154970703-154970847 | Rare:29 | ||||
chr1:154974327-154974751 | Rare:111 | ||||
chr1:154983110-154983392 | Common:2; Rare:56; Clinvar (benign):1 |