Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23789900-23790502 | Common:1; Rare:194 | ||||
chr1:23790672-23791439 | Common:1; Rare:492 | ||||
chr1:23791727-23792127 | Common:1; Rare:113 | ||||
chr1:23799340-23800581 | Common:7; Rare:700; Clinvar:4; Clinvar (benign):2 | ||||
chr1:23800510-23801050 | Common:7; Rare:799 | ||||
chr1:23825300-23825780 | Common:26; Rare:501; Clinvar:7; Clinvar (benign):17; Clinvar (pathogenic):15 | ||||
chr1:23825802-23826394 | Common:6; Rare:166 | ||||
chr1:23838497-23838897 | Common:3; Rare:88 | ||||
chr1:23868237-23868688 | Common:29; Rare:434; Clinvar:8; Clinvar (benign):22 | ||||
chr1:23868750-23869170 | Common:9; Rare:143 | ||||
chr1:23958910-23960009 | Common:42; Rare:923 | ||||
chr1:23960020-23960969 | Common:20; Rare:515 | ||||
chr1:23976791-23978328 | Common:1; Rare:315 | ||||
chr1:23979371-23980100 | Common:13; Rare:327 | ||||
chr1:23980191-23980635 | Common:5; Rare:682 |