Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:2950602-2950927 | Common:2; Rare:96 | ||||
chr19:3984208-3984599 | Common:5; Rare:154; Clinvar:2; Clinvar (benign):2 | ||||
chr19:4280258-4280356 | Rare:38 | ||||
chr19:7198101-7198295 | Common:3; Rare:69 | ||||
chr19:8161253-8161454 | Common:3; Rare:41 | ||||
chr19:8506253-8506381 | Common:1; Rare:30 | ||||
chr19:9406975-9407345 | Common:5; Rare:104 | ||||
chr19:11639428-11639862 | Common:4; Rare:102 | ||||
chr19:12194827-12195040 | Common:2; Rare:75 | ||||
chr19:12788684-12788807 | Rare:24 | ||||
chr19:12793469-12793749 | Common:3; Rare:75 | ||||
chr19:12810131-12810331 | Common:1; Rare:71; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:13152710-13152742 | Rare:7 | ||||
chr19:13152856-13153056 | Rare:62 | ||||
chr19:13155508-13155758 | Common:1; Rare:53 |