Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:100088941-100089126 | Rare:71; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:102402351-102402439 | Rare:14 | ||||
chr13:102596773-102597028 | Common:1; Rare:116 | ||||
chr13:102798906-102799124 | Common:1; Rare:46 | ||||
chr13:106568097-106568267 | Rare:53 | ||||
chr13:108218347-108218511 | Rare:64 | ||||
chr13:110307110-110307488 | Common:6; Rare:121; Clinvar (benign):8 | ||||
chr13:110915011-110915239 | Common:3; Rare:93 | ||||
chr13:112588130-112588276 | Rare:35 | ||||
chr13:113208610-113208743 | Rare:83 | ||||
chr13:113490676-113491170 | Common:5; Rare:183 | ||||
chr13:113759155-113759227 | Rare:18 | ||||
chr13:113863940-113864183 | Common:2; Rare:62 | ||||
chr14:20343415-20343647 | Common:6; Rare:107 | ||||
chr14:20454804-20455337 | Common:7; Rare:137 |