Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52366106-52366433 | Common:1; Rare:91 | ||||
chr1:52404398-52404637 | Common:1; Rare:71 | ||||
chr1:52553454-52553674 | Common:2; Rare:63 | ||||
chr1:52602306-52602433 | Common:2; Rare:45 | ||||
chr1:52698070-52698162 | Rare:19 | ||||
chr1:52698306-52698460 | Common:2; Rare:58; Clinvar (pathogenic):1 | ||||
chr1:53061540-53061780 | Common:2; Rare:40 | ||||
chr1:53062060-53062290 | Common:5; Rare:55 | ||||
chr1:53220586-53220746 | Common:2; Rare:69 | ||||
chr1:53238437-53238598 | Rare:69 | ||||
chr1:53238606-53238687 | Rare:23 | ||||
chr1:53889731-53889974 | Common:2; Rare:76 | ||||
chr1:53946262-53946509 | Common:2; Rare:88 | ||||
chr1:54053000-54053687 | Common:7; Rare:234 | ||||
chr1:54199985-54200246 | Rare:72 |