Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160262116-160262294 | Rare:50 | ||||
chr1:160343137-160343421 | Rare:109 | ||||
chr1:161021082-161021260 | Common:5; Rare:57 | ||||
chr1:161038744-161038836 | Common:1; Rare:22 | ||||
chr1:161038885-161039018 | Common:1; Rare:48 | ||||
chr1:161045860-161046057 | Common:1; Rare:51 | ||||
chr1:161098074-161098383 | Common:1; Rare:47 | ||||
chr1:161117977-161118146 | Rare:91 | ||||
chr1:161132417-161132681 | Common:1; Rare:91 | ||||
chr1:161215196-161215324 | Common:1; Rare:35 | ||||
chr1:161258653-161258745 | Common:1; Rare:18 | ||||
chr1:161314264-161314419 | Common:3; Rare:61; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161367839-161367905 | Rare:13 | ||||
chr1:161524393-161524540 | Common:3; Rare:47 | ||||
chr1:161749510-161749835 | Common:1; Rare:93 |