Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:77027136-77027293 | Common:5; Rare:50 | ||||
chr13:77919390-77919704 | Common:1; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
chr13:79405776-79405898 | Rare:43 | ||||
chr13:79406219-79406325 | Common:2; Rare:32 | ||||
chr13:79481174-79481467 | Common:1; Rare:128 | ||||
chr13:93227263-93227328 | Rare:12; Clinvar:2 | ||||
chr13:94601548-94601907 | Common:4; Rare:105 | ||||
chr13:95301417-95301566 | Rare:38 | ||||
chr13:95552560-95552806 | Common:1; Rare:83 | ||||
chr13:95552909-95552958 | Rare:20 | ||||
chr13:95676918-95677205 | Common:3; Rare:104 | ||||
chr13:96053239-96053477 | Common:1; Rare:102 | ||||
chr13:97222185-97222402 | Rare:36 | ||||
chr13:99200668-99200900 | Common:6; Rare:109 | ||||
chr13:99307397-99307420 | Rare:2 |