chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 46485711 46485712 T G 9 GENIC homozygous 563279861 6 46485907 46485908 A T 20 GENIC homozygous 563279862 6 46486115 46486116 T TC 5 GENIC heterozygous 708338111 6 46486543 46486544 G C 9 GENIC possibly homozygous 563279863 6 46487298 46487299 C T 18 GENIC possibly homozygous 563279864 6 46487401 46487402 C T 19 GENIC possibly homozygous 563279865 6 46487709 46487710 C CT 2 GENIC homozygous 708338113 6 46487787 46487788 A G 8 GENIC homozygous 563279866 6 46487854 46487855 G - 10 GENIC possibly homozygous 708338114 6 46488146 46488147 C A 5 GENIC homozygous 565202515 6 46488589 46488590 A G 12 GENIC possibly homozygous 563279867 6 46488649 46488650 C G 14 GENIC possibly homozygous 563279868 6 46488948 46488949 G A 9 GENIC possibly homozygous 563279869 6 46489100 46489101 G C 14 GENIC homozygous 563279870 6 46489719 46489720 C T 21 GENIC homozygous 563279871 6 46489750 46489751 C G 12 GENIC heterozygous 563279872 6 46489800 46489801 A G 16 GENIC homozygous 563279873 6 46489815 46489816 C T 18 GENIC homozygous 563279874 6 46489905 46489906 G - 10 GENIC homozygous 708338115 6 46489926 46489927 C T 14 GENIC homozygous 563279875