Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:94601600-94601948 | Common:3; Rare:112 | ||||
chr13:95301389-95301561 | Rare:48 | ||||
chr13:95676936-95677256 | Common:4; Rare:111 | ||||
chr13:96053353-96053603 | Common:2; Rare:101 | ||||
chr13:97222154-97222458 | Rare:55 | ||||
chr13:98978352-98978610 | Common:3; Rare:40 | ||||
chr13:99200668-99200900 | Common:6; Rare:109 | ||||
chr13:100088901-100089117 | Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
chr13:100674774-100675156 | Common:4; Rare:159 | ||||
chr13:102596782-102597041 | Common:1; Rare:120 | ||||
chr13:102773716-102773842 | Rare:59 | ||||
chr13:102798920-102799201 | Common:1; Rare:58 | ||||
chr13:102845689-102846116 | Common:9; Rare:118; Clinvar:3; Clinvar (benign):4 | ||||
chr13:106568038-106568267 | Rare:64 | ||||
chr13:108218321-108218520 | Rare:78 |