Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:30616959-30617141 | Rare:32 | ||||
chr13:30617479-30618046 | Common:1; Rare:184 | ||||
chr13:33205992-33206146 | Rare:32 | ||||
chr13:33285670-33286018 | Common:1; Rare:72 | ||||
chr13:33818045-33818190 | Rare:66 | ||||
chr13:35476687-35476822 | Common:1; Rare:21 | ||||
chr13:36346270-36346454 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr13:36999302-36999457 | Rare:59 | ||||
chr13:37059600-37059726 | Common:1; Rare:45 | ||||
chr13:37598607-37598836 | Common:2; Rare:71 | ||||
chr13:38349676-38349932 | Common:3; Rare:95; Clinvar (pathogenic):1 | ||||
chr13:38350215-38350422 | Rare:66 | ||||
chr13:39038087-39038482 | Common:1; Rare:97 | ||||
chr13:40771138-40771344 | Common:3; Rare:67 | ||||
chr13:40982860-40983032 | Common:3; Rare:27 |