Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151281958-151282318 | Rare:103 | ||||
chr1:151346854-151347015 | Rare:47 | ||||
chr1:151399460-151399786 | Common:4; Rare:102; Clinvar (pathogenic):2 | ||||
chr1:151459166-151459257 | Rare:31 | ||||
chr1:151763426-151763570 | Common:2; Rare:55 | ||||
chr1:151790461-151790871 | Common:3; Rare:94 | ||||
chr1:151909397-151909710 | Common:4; Rare:112 | ||||
chr1:151992539-151992813 | Common:2; Rare:59 | ||||
chr1:151993750-151994008 | Common:4; Rare:93 | ||||
chr1:152036912-152037081 | Common:2; Rare:46 | ||||
chr1:153535903-153536099 | Common:2; Rare:45 | ||||
chr1:153544973-153545251 | Common:1; Rare:45 | ||||
chr1:153545751-153545870 | Rare:20 | ||||
chr1:153545877-153545926 | Rare:9 | ||||
chr1:153549039-153549209 | Common:2; Rare:25 |