Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:98142246-98142694 | Common:1; Rare:117 | ||||
chr13:98576219-98576293 | Common:1; Rare:20 | ||||
chr13:98977898-98978181 | Common:2; Rare:63 | ||||
chr13:99200667-99200915 | Common:6; Rare:116 | ||||
chr13:99307339-99307591 | Common:2; Rare:35 | ||||
chr13:99312582-99312837 | Rare:36 | ||||
chr13:99606531-99606713 | Common:5; Rare:60 | ||||
chr13:100088894-100089167 | Rare:102; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr13:100674774-100675060 | Common:3; Rare:117 | ||||
chr13:102402416-102402446 | Rare:8 | ||||
chr13:102596761-102597057 | Common:1; Rare:133; Clinvar (benign):1 | ||||
chr13:102773716-102773879 | Rare:69 | ||||
chr13:102798933-102799363 | Common:1; Rare:87 | ||||
chr13:102845734-102846286 | Common:10; Rare:145; Clinvar:5; Clinvar (benign):6 | ||||
chr13:106567583-106568267 | Rare:196 |