Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19294772-19294860 | Rare:9 | ||||
chr1:20651688-20651788 | Common:3; Rare:25 | ||||
chr1:20654223-20654705 | Common:5; Rare:150; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:20755078-20755279 | Rare:40 | ||||
chr1:20756428-20756716 | Common:1; Rare:64 | ||||
chr1:21084194-21084490 | Common:4; Rare:63 | ||||
chr1:21841304-21841591 | Common:2; Rare:60; Clinvar:1 | ||||
chr1:21851801-21852135 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
chr1:21855629-21855870 | Common:3; Rare:83; Clinvar:5; Clinvar (benign):3 | ||||
chr1:21872343-21872430 | Rare:25; Clinvar:1 | ||||
chr1:22025015-22025136 | Rare:25 | ||||
chr1:22025444-22025563 | Common:6; Rare:41 | ||||
chr1:22077100-22077140 | Rare:6 | ||||
chr1:22090981-22091018 | Rare:6 | ||||
chr1:22502012-22502313 | Rare:60 |