Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:8390043-8390412 | Common:1; Rare:105 | ||||
chr19:8514112-8514226 | Common:2; Rare:34 | ||||
chr19:9140319-9140428 | Rare:30 | ||||
chr19:9538581-9538745 | Common:1; Rare:49 | ||||
chr19:9621178-9621562 | Common:3; Rare:109 | ||||
chr19:9827819-9827948 | Common:1; Rare:46 | ||||
chr19:10315994-10316286 | Common:1; Rare:88; Clinvar (benign):4 | ||||
chr19:10333508-10333715 | Rare:69 | ||||
chr19:10653841-10654128 | Common:1; Rare:109 | ||||
chr19:10836268-10836577 | Common:3; Rare:79 | ||||
chr19:10928538-10928873 | Common:2; Rare:110 | ||||
chr19:11197489-11197637 | Common:1; Rare:42 | ||||
chr19:11435122-11435459 | Common:3; Rare:86; Clinvar (benign):1 | ||||
chr19:11559207-11559413 | Common:1; Rare:63 | ||||
chr19:12610807-12610989 | Rare:67 |