Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244863982-244864686 | Common:1; Rare:243; Clinvar:3; Clinvar (benign):5 | ||||
chr1:244969450-244969818 | Common:1; Rare:99 | ||||
chr1:244969991-244970418 | Common:5; Rare:174 | ||||
chr1:246566155-246566591 | Common:3; Rare:148 | ||||
chr1:246566980-246567243 | Common:1; Rare:57 | ||||
chr1:247078753-247078877 | Rare:35 | ||||
chr1:247331173-247331325 | Rare:41 | ||||
chr1:247331679-247331807 | Rare:35 | ||||
chr1:248825848-248826021 | Common:3; Rare:51 | ||||
chr1:248838053-248838373 | Common:2; Rare:102 | ||||
chr1:248838759-248838822 | Rare:12 | ||||
chr1:248858919-248859168 | Rare:96 | ||||
chr10:134614-134806 | Rare:52 | ||||
chr10:649745-650008 | Common:1; Rare:63 | ||||
chr10:650022-650143 | Rare:29 |