Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37690479-37690736 | Common:6; Rare:69 | ||||
chr1:37692229-37692489 | Common:3; Rare:54 | ||||
chr1:37808176-37808296 | Rare:31 | ||||
chr1:37859553-37859780 | Common:3; Rare:74 | ||||
chr1:37989953-37990196 | Rare:83 | ||||
chr1:38859712-38859940 | Rare:84 | ||||
chr1:38873292-38873540 | Common:3; Rare:83 | ||||
chr1:39408769-39409083 | Common:5; Rare:111 | ||||
chr1:39883440-39883590 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
chr1:40039972-40040248 | Common:2; Rare:56 | ||||
chr1:40040457-40040807 | Common:3; Rare:107 | ||||
chr1:40161276-40161399 | Rare:31 | ||||
chr1:40257903-40258326 | Common:4; Rare:122; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40374600-40374645 | Common:7; Rare:13 | ||||
chr1:40508662-40508773 | Common:3; Rare:30 |