Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21852393-21852571 | Common:5; Rare:56 | ||||
chr1:21865740-21866070 | Common:2; Rare:83; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:21866090-21866490 | Common:1; Rare:153 | ||||
chr1:21900049-21900449 | Common:2; Rare:97 | ||||
chr1:21909750-21910130 | Common:8; Rare:112 | ||||
chr1:21957300-21957700 | Common:5; Rare:81 | ||||
chr1:22019060-22019330 | Common:2; Rare:86 | ||||
chr1:22024495-22024636 | Common:2; Rare:26 | ||||
chr1:22024930-22025245 | Rare:91 | ||||
chr1:22025185-22025640 | Common:30; Rare:286 | ||||
chr1:22025760-22026195 | Common:8; Rare:379 | ||||
chr1:22026226-22026401 | Rare:33 | ||||
chr1:22026941-22027542 | Common:16; Rare:159 | ||||
chr1:22031413-22031813 | Common:2; Rare:131 | ||||
chr1:22039820-22040190 | Common:13; Rare:164 |