Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:200612767-200612871 | Common:1; Rare:19 | ||||
chr1:200762069-200762205 | Rare:25 | ||||
chr1:200768902-200768919 | Rare:1 | ||||
chr1:200776777-200776812 | Rare:4 | ||||
chr1:200782457-200782764 | Common:2; Rare:43 | ||||
chr1:200811711-200811999 | Rare:54 | ||||
chr1:200813855-200814178 | Common:5; Rare:54 | ||||
chr1:200845097-200845212 | Rare:12 | ||||
chr1:200864155-200864161 | |||||
chr1:201266868-201267040 | Common:1; Rare:39 | ||||
chr1:201308176-201308378 | Common:4; Rare:53 | ||||
chr1:201325674-201325848 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr1:201326136-201326192 | Rare:8 | ||||
chr1:201339664-201339747 | Rare:17 | ||||
chr1:201402568-201402613 | Common:1; Rare:5 |