Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:100088948-100089117 | Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
chr13:100674787-100675060 | Common:3; Rare:110 | ||||
chr13:102596792-102597035 | Common:1; Rare:115 | ||||
chr13:102773725-102773879 | Rare:67 | ||||
chr13:102798991-102799168 | Rare:39 | ||||
chr13:102845734-102846103 | Common:8; Rare:97; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106568078-106568278 | Rare:62 | ||||
chr13:108218307-108218520 | Rare:82 | ||||
chr13:110713018-110713263 | Common:2; Rare:106 | ||||
chr13:111153610-111153714 | Common:2; Rare:45 | ||||
chr13:113208627-113208741 | Rare:66 | ||||
chr13:113490699-113491170 | Common:4; Rare:176 | ||||
chr13:114234761-114235065 | Common:15; Rare:113 | ||||
chr13:114281501-114281654 | Common:2; Rare:82 | ||||
chr14:20343219-20343655 | Common:12; Rare:246 |