Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:107825192-107825242 | Rare:9 | ||||
chr4:107989663-107989979 | Common:6; Rare:136; Clinvar:4; Clinvar (benign):5 | ||||
chr4:108620373-108620717 | Common:6; Rare:156 | ||||
chr4:109433756-109433930 | Common:1; Rare:60 | ||||
chr4:109729600-109729789 | Rare:68 | ||||
chr4:109815475-109815804 | Common:1; Rare:88 | ||||
chr4:110623067-110623282 | Common:1; Rare:46 | ||||
chr4:112231586-112231897 | Common:2; Rare:95 | ||||
chr4:112285761-112285978 | Rare:67 | ||||
chr4:112297227-112297448 | Common:1; Rare:35 | ||||
chr4:112636862-112637187 | Common:1; Rare:90 | ||||
chr4:112637394-112637576 | Common:3; Rare:49 | ||||
chr4:113049616-113049706 | Rare:17; Clinvar (benign):1 | ||||
chr4:113761113-113761243 | Common:1; Rare:33 | ||||
chr4:113761268-113761357 | Rare:15 |