chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 59331098 59331099 A G 17 GENIC homozygous 579797911 8 59331528 59331529 T C 28 GENIC homozygous 579797912 8 59333429 59333430 A G 20 GENIC homozygous 579797913 8 59335154 59335155 A G 26 GENIC homozygous 579797914 8 59336407 59336408 C T 19 GENIC possibly homozygous 581350255 8 59339280 59339281 A G 24 GENIC possibly homozygous 579797915 8 59340035 59340036 C T 14 GENIC homozygous 581350256 8 59341967 59341968 A G 3 GENIC heterozygous 579797916 8 59342127 59342128 T C 16 GENIC possibly homozygous 579797917 8 59342724 59342725 G A 23 GENIC possibly homozygous 579797918 8 59346334 59346335 G GAGC 10 GENIC homozygous 717793226 8 59350439 59350440 G A 9 GENIC possibly homozygous 579797919 8 59356424 59356425 C - 4 GENIC homozygous 717793227 8 59357717 59357718 G A 19 GENIC possibly homozygous 579797920 8 59357827 59357831 CTCT ---- 2 GENIC heterozygous 717793228 8 59364716 59364717 T C 20 GENIC homozygous 579797921 8 59365391 59365392 T C 22 GENIC homozygous 579797922 8 59365714 59365715 G A 22 GENIC possibly homozygous 581350257 8 59365914 59365915 C A 18 GENIC possibly homozygous 579797923 8 59368350 59368351 C T 24 GENIC possibly homozygous 581350258