Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:45341170-45341451 | Common:4; Rare:116 | ||||
chr13:49247816-49247947 | Rare:35 | ||||
chr13:49444005-49444274 | Common:1; Rare:91 | ||||
chr13:102596782-102597017 | Common:1; Rare:103 | ||||
chr13:102798922-102799180 | Common:1; Rare:53 | ||||
chr13:108218313-108218520 | Rare:80 | ||||
chr13:110307155-110307296 | Rare:47 | ||||
chr13:113208638-113208694 | Rare:37 | ||||
chr14:20455051-20455259 | Common:2; Rare:61 | ||||
chr14:20684490-20684618 | Common:1; Rare:21; Clinvar (benign):1 | ||||
chr14:22766545-22766716 | Common:1; Rare:91 | ||||
chr14:24232321-24232465 | Common:6; Rare:35 | ||||
chr14:24442767-24443010 | Common:5; Rare:70 | ||||
chr14:34982727-34983011 | Common:4; Rare:78 | ||||
chr14:35122269-35122574 | Common:1; Rare:93 |