Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111200121-111200327 | Common:3; Rare:30 | ||||
chr1:111200629-111200770 | Rare:31 | ||||
chr1:111204321-111204603 | Rare:66 | ||||
chr1:111473766-111474010 | Common:2; Rare:54 | ||||
chr1:111619559-111619918 | Common:2; Rare:110 | ||||
chr1:111739339-111739560 | Common:2; Rare:57 | ||||
chr1:112396003-112396265 | Common:1; Rare:82 | ||||
chr1:112619075-112619236 | Rare:61 | ||||
chr1:112619642-112619877 | Common:2; Rare:84 | ||||
chr1:112707080-112707230 | Rare:52 | ||||
chr1:112956150-112956496 | Common:5; Rare:144; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073081-113073250 | Common:1; Rare:63 | ||||
chr1:113390205-113390532 | Common:1; Rare:82 | ||||
chr1:113759524-113759572 | Common:1; Rare:11 | ||||
chr1:113812228-113812551 | Common:2; Rare:137 |