Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243255783-243256107 | Rare:86; Clinvar:4 | ||||
chr1:243487674-243487853 | Common:3; Rare:48 | ||||
chr1:244451686-244452005 | Rare:96 | ||||
chr1:244835566-244835736 | Common:2; Rare:72; Clinvar (benign):4 | ||||
chr1:244864185-244864686 | Rare:173; Clinvar:1; Clinvar (benign):1 | ||||
chr1:244970249-244970420 | Common:3; Rare:78 | ||||
chr1:246566209-246566563 | Common:1; Rare:114 | ||||
chr1:247007993-247008263 | Common:2; Rare:63 | ||||
chr1:247078728-247078896 | Common:1; Rare:51 | ||||
chr1:248825857-248826030 | Common:3; Rare:51 | ||||
chr1:248837998-248838303 | Common:1; Rare:115 | ||||
chr1:248906585-248906843 | Common:4; Rare:77 | ||||
chr10:988272-988482 | Common:3; Rare:82 | ||||
chr10:1048874-1049108 | Common:2; Rare:118 | ||||
chr10:1056702-1056878 | Common:3; Rare:63 |