Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231366394-231366555 | Common:7; Rare:50; Clinvar (benign):3 | ||||
chr1:231370596-231370866 | Common:2; Rare:55 | ||||
chr1:231395407-231395689 | Common:4; Rare:40 | ||||
chr1:231420992-231421478 | Common:1; Rare:153; Clinvar:5; Clinvar (benign):4 | ||||
chr1:234140064-234140269 | Common:2; Rare:42 | ||||
chr1:234144930-234145058 | Common:1; Rare:22 | ||||
chr1:234396142-234396244 | Common:1; Rare:17 | ||||
chr1:234610157-234610296 | Common:1; Rare:57 | ||||
chr1:234611471-234611719 | Common:1; Rare:55 | ||||
chr1:234723766-234723864 | Common:1; Rare:16 | ||||
chr1:234962592-234962926 | Rare:67 | ||||
chr1:234980747-234980876 | Rare:19 | ||||
chr1:234997266-234997580 | Common:1; Rare:59 | ||||
chr1:235131926-235132205 | Rare:75 | ||||
chr1:235908986-235909225 | Rare:41 |