chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 30439381 30439382 G A 16 GENIC heterozygous 50170474 12 30439471 30439472 T G 7 GENIC heterozygous 50170476 12 30439473 30439474 T C 8 GENIC heterozygous 50170478 12 30440672 30440673 T - 30 GENIC heterozygous 50170480 12 30555767 30555768 G A 15 GENIC heterozygous 50410999 12 30572445 30572446 C G 34 GENIC heterozygous 50590445 12 30582452 30582453 C T 10 GENIC heterozygous 50411042 12 30603801 30603802 A G 45 GENIC heterozygous 50590485 12 30667663 30667664 C A 16 GENIC heterozygous 50590662 12 30667734 30667735 A G 32 GENIC heterozygous 50171785 12 30682651 30682652 C T 38 GENIC heterozygous 50590676 12 30683935 30683936 A G 14 GENIC heterozygous 50171876 12 30695664 30695665 C CT 53 GENIC heterozygous 50376551 12 30703058 30703059 T C 23 GENIC heterozygous 50376615 12 30725914 30725928 GGAAGAGGTCTGCC -------------- 20 GENIC heterozygous 50376975 12 30725934 30725935 A - 16 GENIC heterozygous 50376977 12 30771414 30771415 G A 33 GENIC heterozygous 50172076 12 30771499 30771500 C A 27 GENIC heterozygous 50172077 12 30771522 30771523 G GT 30 GENIC heterozygous 50377131 12 30771751 30771752 A T 14 GENIC heterozygous 50172079 12 30785559 30785560 T C 33 GENIC heterozygous 50377196 12 30787454 30787455 G C 34 GENIC heterozygous 50172168 12 30799411 30799412 G C 27 GENIC heterozygous 50377222 12 30799595 30799596 C T 16 GENIC heterozygous 50377224 12 30804180 30804181 T C 33 GENIC heterozygous 50172251 12 30827757 30827758 A G 13 GENIC heterozygous 50377264 12 30827799 30827800 A G 11 GENIC heterozygous 50377266