Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207589488-207589689 | Rare:41 | ||||
chr1:207784977-207785106 | Common:1; Rare:27; Clinvar (benign):1 | ||||
chr1:207822679-207822922 | Common:1; Rare:50 | ||||
chr1:207823965-207824018 | Rare:9 | ||||
chr1:207824028-207824102 | Common:1; Rare:11 | ||||
chr1:207848296-207848478 | Rare:30 | ||||
chr1:207863361-207863459 | Rare:10 | ||||
chr1:207867920-207868104 | Common:1; Rare:38 | ||||
chr1:207962836-207962932 | Common:1; Rare:22 | ||||
chr1:209762761-209763092 | Common:1; Rare:84 | ||||
chr1:209766119-209766244 | Rare:22 | ||||
chr1:211382730-211382854 | Common:1; Rare:51 | ||||
chr1:211577816-211577944 | Rare:27 | ||||
chr1:211578065-211578102 | Rare:12 | ||||
chr1:212138610-212138725 | Rare:27 |