Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36397881-36398016 | Common:2; Rare:33 | ||||
chr1:36450423-36450564 | Rare:41 | ||||
chr1:36464230-36464468 | Common:2; Rare:69 | ||||
chr1:37690502-37690696 | Common:5; Rare:48 | ||||
chr1:37692193-37692577 | Common:4; Rare:92 | ||||
chr1:37859586-37859784 | Common:3; Rare:64 | ||||
chr1:37989961-37990218 | Rare:87 | ||||
chr1:38873309-38873554 | Common:3; Rare:84 | ||||
chr1:39026166-39026394 | Common:1; Rare:55 | ||||
chr1:39738734-39738898 | Common:2; Rare:33 | ||||
chr1:40040451-40040801 | Common:3; Rare:106 | ||||
chr1:40097228-40097319 | Rare:36; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:40161145-40161420 | Common:1; Rare:74 | ||||
chr1:40257903-40258255 | Common:4; Rare:91; Clinvar:6 | ||||
chr1:40450041-40450145 | Common:1; Rare:37 |