Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37692183-37692564 | Common:4; Rare:87 | ||||
chr1:37808284-37808667 | Common:1; Rare:87 | ||||
chr1:37859544-37859834 | Common:4; Rare:102 | ||||
chr1:37989914-37990173 | Rare:89 | ||||
chr1:38859686-38859940 | Rare:100 | ||||
chr1:38873292-38873554 | Common:3; Rare:87 | ||||
chr1:38941706-38941890 | Rare:43 | ||||
chr1:39026155-39026398 | Common:1; Rare:58 | ||||
chr1:39883428-39883594 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:40039937-40040268 | Common:3; Rare:72 | ||||
chr1:40040463-40040807 | Common:3; Rare:105 | ||||
chr1:40161276-40161405 | Rare:33 | ||||
chr1:40257898-40258309 | Common:4; Rare:113; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40344649-40344850 | Rare:32 | ||||
chr1:40373544-40373794 | Common:1; Rare:64 |