Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151399378-151399635 | Common:3; Rare:82; Clinvar (pathogenic):2 | ||||
chr1:151612435-151612468 | Rare:10 | ||||
chr1:151716769-151717020 | Common:1; Rare:81 | ||||
chr1:151721218-151721539 | Common:2; Rare:78 | ||||
chr1:151763451-151763541 | Common:1; Rare:33 | ||||
chr1:151790426-151790876 | Common:3; Rare:111 | ||||
chr1:151909396-151909569 | Common:1; Rare:68 | ||||
chr1:153357667-153357881 | Common:1; Rare:39 | ||||
chr1:153535937-153536088 | Common:1; Rare:33 | ||||
chr1:153536217-153536282 | Rare:10 | ||||
chr1:153545787-153545862 | Rare:10 | ||||
chr1:153628236-153628456 | Common:1; Rare:51 | ||||
chr1:153633851-153634123 | Common:4; Rare:85 | ||||
chr1:153658416-153658773 | Common:2; Rare:75 | ||||
chr1:153727775-153728082 | Common:1; Rare:90 |