Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150257958-150258071 | Common:2; Rare:30 | ||||
chr1:150268279-150268541 | Rare:52 | ||||
chr1:150282293-150282572 | Common:3; Rare:49 | ||||
chr1:150629549-150629819 | Rare:51 | ||||
chr1:151165851-151166157 | Common:3; Rare:86 | ||||
chr1:151346867-151347048 | Rare:48 | ||||
chr1:151611955-151612075 | Common:1; Rare:26 | ||||
chr1:151790458-151790837 | Common:2; Rare:87 | ||||
chr1:153608916-153609015 | Common:1; Rare:13 | ||||
chr1:153628231-153628444 | Common:1; Rare:50 | ||||
chr1:153634033-153634146 | Rare:38 | ||||
chr1:153658592-153658731 | Common:2; Rare:36 | ||||
chr1:153963484-153963672 | Common:2; Rare:49 | ||||
chr1:153967718-153967934 | Rare:39 | ||||
chr1:154170418-154170681 | Rare:56; Clinvar (benign):1 |