Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151372648-151372785 | Common:1; Rare:60 | ||||
chr1:151399280-151399594 | Common:3; Rare:119; Clinvar (pathogenic):2 | ||||
chr1:151459338-151459730 | Common:4; Rare:231 | ||||
chr1:151511129-151511436 | Common:8; Rare:129 | ||||
chr1:151611844-151612225 | Common:4; Rare:151; Clinvar (benign):1 | ||||
chr1:151763413-151763579 | Common:3; Rare:108 | ||||
chr1:151790458-151790874 | Common:3; Rare:98 | ||||
chr1:151909377-151909730 | Common:8; Rare:248 | ||||
chr1:151992440-151992800 | Common:5; Rare:117 | ||||
chr1:153608700-153609210 | Common:3; Rare:143 | ||||
chr1:153609230-153609540 | Common:4; Rare:71 | ||||
chr1:153628237-153628491 | Common:1; Rare:91 | ||||
chr1:153633820-153634153 | Common:8; Rare:187 | ||||
chr1:153634320-153634600 | Common:4; Rare:143 | ||||
chr1:153658551-153658738 | Common:4; Rare:91 |