Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244863558-244863682 | Rare:53; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:244864346-244864825 | Common:1; Rare:194 | ||||
chr1:244969611-244970036 | Rare:115 | ||||
chr1:244970045-244970452 | Common:5; Rare:179 | ||||
chr1:244970492-244971156 | Common:8; Rare:218 | ||||
chr1:245154514-245154629 | Rare:25 | ||||
chr1:245154808-245155136 | Common:2; Rare:74 | ||||
chr1:246506693-246506941 | Common:3; Rare:55 | ||||
chr1:246507207-246507442 | Common:2; Rare:84 | ||||
chr1:246565835-246566022 | Common:2; Rare:82 | ||||
chr1:246566124-246566608 | Common:3; Rare:161 | ||||
chr1:246566941-246567061 | Rare:31 | ||||
chr1:246724032-246724105 | Common:1; Rare:18 | ||||
chr1:246724166-246724519 | Common:2; Rare:121 | ||||
chr1:246931027-246931194 | Common:2; Rare:62 |