Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193105326-193105524 | Common:5; Rare:156 | ||||
chr1:193121709-193122215 | Common:5; Rare:338; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr1:196651637-196651893 | Common:2; Rare:50 | ||||
chr1:196651933-196652118 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):6 | ||||
chr1:197146165-197146302 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
chr1:197146572-197146883 | Rare:140; Clinvar:6 | ||||
chr1:197774888-197775288 | Common:2; Rare:153 | ||||
chr1:197775202-197775974 | Common:3; Rare:319 | ||||
chr1:197902854-197902997 | Common:3; Rare:135 | ||||
chr1:198156929-198157175 | Rare:168 | ||||
chr1:198157547-198157867 | Common:2; Rare:177 | ||||
chr1:200409944-200410151 | Rare:125 | ||||
chr1:200620646-200620890 | Common:4; Rare:115 | ||||
chr1:200669240-200669651 | Common:5; Rare:161 | ||||
chr1:200669789-200670243 | Common:24; Rare:234 |