Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:201118615-201118800 | Rare:26 | ||||
chr2:201260420-201260585 | Rare:35 | ||||
chr2:201642637-201642996 | Rare:115 | ||||
chr2:201780887-201781186 | Common:2; Rare:92; Clinvar:3; Clinvar (benign):2 | ||||
chr2:202238498-202238687 | Common:1; Rare:65 | ||||
chr2:202912127-202912303 | Common:2; Rare:58 | ||||
chr2:203014676-203014877 | Common:1; Rare:49 | ||||
chr2:203238836-203239026 | Rare:73 | ||||
chr2:203328187-203328443 | Common:2; Rare:97 | ||||
chr2:206159380-206159695 | Common:3; Rare:101; Clinvar (benign):1 | ||||
chr2:206274916-206275018 | Rare:40 | ||||
chr2:206765288-206765674 | Common:3; Rare:103; Clinvar:5; Clinvar (benign):5 | ||||
chr2:207165943-207166142 | Rare:38 | ||||
chr2:207529774-207530001 | Common:3; Rare:70 | ||||
chr2:207625226-207625378 | Common:1; Rare:44 |