Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:75636013-75636363 | Common:2; Rare:85 | ||||
chr13:76992023-76992175 | Rare:67; Clinvar:10; Clinvar (benign):6 | ||||
chr13:77918800-77918932 | Common:1; Rare:30 | ||||
chr13:79405785-79405880 | Rare:37 | ||||
chr13:94601646-94601918 | Common:3; Rare:76 | ||||
chr13:95676918-95677182 | Common:3; Rare:94 | ||||
chr13:96053336-96053477 | Common:1; Rare:64 | ||||
chr13:98977961-98978209 | Common:2; Rare:44 | ||||
chr13:99200668-99200900 | Common:6; Rare:109 | ||||
chr13:100088920-100089117 | Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596785-102597041 | Common:1; Rare:120 | ||||
chr13:102773725-102773842 | Rare:57 | ||||
chr13:102798962-102799150 | Rare:40 | ||||
chr13:108218339-108218520 | Rare:71 | ||||
chr13:110307204-110307486 | Common:5; Rare:82; Clinvar (benign):6 |