Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:203448739-203449020 | Rare:60 | ||||
chr2:204997107-204997122 | Rare:3 | ||||
chr2:206085169-206085267 | Rare:23 | ||||
chr2:214937586-214937645 | Rare:21; Clinvar (pathogenic):1 | ||||
chr2:214954774-214954920 | Common:2; Rare:21 | ||||
chr2:214966902-214967146 | Common:2; Rare:47; Clinvar (pathogenic):1 | ||||
chr2:214974815-214975146 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr2:214988527-214988732 | Common:1; Rare:35 | ||||
chr2:215000971-215001092 | Rare:33; Clinvar:1 | ||||
chr2:215004351-215004448 | Rare:12 | ||||
chr2:215006988-215007009 | Rare:2 | ||||
chr2:215012026-215012331 | Rare:60; Clinvar:1 | ||||
chr2:215015521-215015827 | Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
chr2:215030550-215030679 | Common:1; Rare:22 | ||||
chr2:215048639-215048741 | Common:3; Rare:18 |