Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37807722-37807824 | Rare:41 | ||||
chr1:37808153-37808602 | Common:2; Rare:118 | ||||
chr1:37859581-37859797 | Common:3; Rare:71 | ||||
chr1:37989970-37990226 | Common:1; Rare:86 | ||||
chr1:38012524-38012856 | Rare:100 | ||||
chr1:38873293-38873540 | Common:3; Rare:83 | ||||
chr1:38941768-38941886 | Rare:24 | ||||
chr1:38991432-38991541 | Common:1; Rare:30 | ||||
chr1:39026246-39026401 | Common:1; Rare:41 | ||||
chr1:39788840-39789024 | Common:2; Rare:66 | ||||
chr1:39955004-39955152 | Common:1; Rare:35 | ||||
chr1:40040457-40040834 | Common:3; Rare:113 | ||||
chr1:40161255-40161399 | Rare:37 | ||||
chr1:40257898-40258384 | Common:4; Rare:141; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40508657-40508769 | Common:3; Rare:29 |