Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151346796-151347079 | Rare:77 | ||||
chr1:151347211-151347492 | Rare:66 | ||||
chr1:151347790-151347846 | Rare:11 | ||||
chr1:151399361-151399602 | Common:2; Rare:66; Clinvar (pathogenic):1 | ||||
chr1:151763497-151763551 | Common:1; Rare:15 | ||||
chr1:151790458-151790856 | Common:2; Rare:92 | ||||
chr1:151909400-151909662 | Common:3; Rare:100 | ||||
chr1:151993782-151993891 | Common:3; Rare:35 | ||||
chr1:153545748-153545772 | Rare:4 | ||||
chr1:153545804-153545888 | Rare:17 | ||||
chr1:153628189-153628411 | Common:1; Rare:53 | ||||
chr1:153633749-153634120 | Common:6; Rare:106 | ||||
chr1:153634331-153634498 | Common:1; Rare:53 | ||||
chr1:153670918-153671311 | Rare:165 | ||||
chr1:153941975-153942231 | Common:2; Rare:70 |