Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:98142368-98142662 | Common:1; Rare:80 | ||||
chr13:99200668-99200900 | Common:6; Rare:109 | ||||
chr13:99307397-99307523 | Common:1; Rare:16 | ||||
chr13:99606475-99606704 | Common:6; Rare:71 | ||||
chr13:100088745-100089230 | Rare:181; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr13:100674778-100675156 | Common:4; Rare:157 | ||||
chr13:102596773-102597102 | Common:1; Rare:134; Clinvar (benign):1 | ||||
chr13:102773709-102773847 | Rare:62 | ||||
chr13:102798915-102799302 | Common:1; Rare:74 | ||||
chr13:102845749-102846162 | Common:8; Rare:102; Clinvar:4; Clinvar (benign):4 | ||||
chr13:106567841-106568267 | Rare:117 | ||||
chr13:108218256-108218538 | Common:2; Rare:100 | ||||
chr13:110507482-110507634 | Rare:22 | ||||
chr13:110561664-110561900 | Common:5; Rare:83 | ||||
chr13:110615517-110615723 | Rare:81 |