Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155940734-155940959 | Rare:33 | ||||
chr1:155944825-155945064 | Common:1; Rare:52 | ||||
chr1:155979976-155980257 | Rare:61 | ||||
chr1:155983401-155984162 | Rare:170 | ||||
chr1:156001020-156001430 | Rare:129 | ||||
chr1:156104060-156104507 | Common:4; Rare:159 | ||||
chr1:156105014-156105459 | Common:5; Rare:180 | ||||
chr1:156115269-156115649 | Common:1; Rare:84; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:156115910-156116519 | Rare:239 | ||||
chr1:156123706-156124106 | Common:2; Rare:101 | ||||
chr1:156130121-156130790 | Common:8; Rare:289; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
chr1:156239251-156239938 | Common:3; Rare:181 | ||||
chr1:156310773-156311360 | Common:7; Rare:171 | ||||
chr1:156379603-156379749 | Common:1; Rare:30 | ||||
chr1:156456446-156457271 | Common:5; Rare:294 |