Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23434262-23434443 | Common:1; Rare:59 | ||||
chr1:23754206-23754376 | Rare:49 | ||||
chr1:23804386-23804625 | Rare:66; Clinvar:3; Clinvar (pathogenic):2 | ||||
chr1:23994497-23994744 | Common:2; Rare:7 | ||||
chr1:24321904-24321976 | Common:1; Rare:11 | ||||
chr1:25796688-25796733 | Common:2; Rare:4 | ||||
chr1:25808767-25809052 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):5 | ||||
chr1:25875493-25875780 | Rare:76 | ||||
chr1:26452683-26452770 | Rare:21 | ||||
chr1:26457494-26457828 | Common:4; Rare:60 | ||||
chr1:26697186-26697489 | Common:1; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
chr1:26698232-26698425 | Rare:48 | ||||
chr1:26941453-26941814 | Rare:109 | ||||
chr1:26942657-26943059 | Rare:128 | ||||
chr1:26945902-26946144 | Common:1; Rare:48 |