Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:96053327-96053592 | Common:2; Rare:114 | ||||
chr13:99200674-99200907 | Common:6; Rare:111 | ||||
chr13:100088859-100089207 | Rare:136; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr13:101452309-101452723 | Common:4; Rare:78 | ||||
chr13:102596785-102597039 | Common:1; Rare:119 | ||||
chr13:102798933-102799211 | Common:1; Rare:58 | ||||
chr13:102845933-102846129 | Common:3; Rare:49; Clinvar:3; Clinvar (benign):1 | ||||
chr13:106567576-106567869 | Rare:86 | ||||
chr13:106568105-106568278 | Rare:54 | ||||
chr13:108218307-108218512 | Rare:77 | ||||
chr13:110307110-110307512 | Common:6; Rare:125; Clinvar (benign):8 | ||||
chr13:110307590-110307927 | Common:3; Rare:98 | ||||
chr13:112588130-112588214 | Rare:21 | ||||
chr13:113208626-113208756 | Rare:75 | ||||
chr13:113209456-113209633 | Common:3; Rare:54 |