chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 52775783 52775784 G A 34 GENIC homozygous 560919411 9 52775878 52775879 A T 25 GENIC homozygous 560919412 9 52778921 52778922 A - 33 GENIC homozygous 707512855 9 52778988 52778989 G C 33 GENIC homozygous 560919413 9 52780477 52780478 T C 19 GENIC homozygous 560919414 9 52780870 52780871 G A 15 GENIC homozygous 560919415 9 52780926 52780927 A G 13 GENIC homozygous 559898884 9 52780940 52780941 A G 13 GENIC homozygous 559898885 9 52781031 52781032 C T 13 GENIC homozygous 560919416 9 52781073 52781074 T C 7 GENIC homozygous 559898886 9 52781534 52781537 ATC --- 37 GENIC homozygous 707512856 9 52782297 52782298 C A 46 GENIC homozygous 560919417 9 52783384 52783385 G - 17 GENIC possibly homozygous 707512857 9 52783602 52783603 T C 28 GENIC homozygous 559898887 9 52783858 52783859 C CGGGGG 11 GENIC homozygous 707512859 9 52784099 52784100 A G 10 GENIC homozygous 559898888