Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:50459302-50459537 | Common:2; Rare:111; Clinvar:4 | ||||
chr22:50462441-50462583 | Common:4; Rare:67; Clinvar (benign):1 | ||||
chr3:3152440-3152752 | Common:3; Rare:109; Clinvar:1 | ||||
chr3:4981030-4981138 | Rare:21 | ||||
chr3:4981193-4981773 | Common:6; Rare:136 | ||||
chr3:4982392-4982818 | Common:2; Rare:82 | ||||
chr3:8848672-8848937 | Rare:51 | ||||
chr3:9391244-9391295 | Rare:20 | ||||
chr3:9395649-9395862 | Common:1; Rare:65 | ||||
chr3:9396231-9396321 | Rare:40 | ||||
chr3:9443985-9444136 | Common:1; Rare:28 | ||||
chr3:9453804-9454082 | Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
chr3:9467826-9468152 | Common:2; Rare:55 | ||||
chr3:10279073-10279402 | Common:3; Rare:46 | ||||
chr3:10297000-10297277 | Common:3; Rare:52 |