Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42035810-42036185 | Common:3; Rare:253 | ||||
chr1:42335103-42335739 | Common:21; Rare:513 | ||||
chr1:42380624-42380884 | Common:2; Rare:131 | ||||
chr1:42380910-42381420 | Common:2; Rare:204 | ||||
chr1:42455978-42456330 | Rare:175 | ||||
chr1:42456253-42456746 | Common:7; Rare:383 | ||||
chr1:42456839-42457016 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
chr1:42462975-42463376 | Common:8; Rare:241 | ||||
chr1:42658229-42658594 | Common:6; Rare:241 | ||||
chr1:42658686-42659086 | Common:3; Rare:253 | ||||
chr1:42659030-42659290 | Common:1; Rare:65 | ||||
chr1:42682004-42682544 | Common:6; Rare:371 | ||||
chr1:42683031-42684051 | Common:6; Rare:557 | ||||
chr1:42766957-42767391 | Common:17; Rare:388; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:42816916-42817620 | Common:3; Rare:424 |