chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 46485711 46485712 T G 11 GENIC homozygous 54876787 6 46485907 46485908 A T 16 GENIC homozygous 54876788 6 46486115 46486116 T TC 20 GENIC homozygous 54876789 6 46486543 46486544 G C 12 GENIC homozygous 54876790 6 46487298 46487299 C T 29 GENIC homozygous 54876791 6 46487401 46487402 C T 22 GENIC homozygous 54876792 6 46487709 46487710 C CT 6 GENIC homozygous 54876793 6 46487787 46487788 A G 16 GENIC homozygous 54876794 6 46487854 46487855 G - 22 GENIC homozygous 54876795 6 46488142 46488143 C T 21 GENIC homozygous 54876798 6 46488589 46488590 A G 14 GENIC homozygous 54876799 6 46488649 46488650 C G 20 GENIC homozygous 54876800 6 46488701 46488702 T C 17 GENIC homozygous 54876801 6 46488948 46488949 G A 23 GENIC homozygous 54876802 6 46489100 46489101 G C 20 GENIC homozygous 54876803 6 46489719 46489720 C T 21 GENIC homozygous 54876804 6 46489750 46489751 C G 27 GENIC homozygous 54876805 6 46489800 46489801 A G 30 GENIC homozygous 54876806 6 46489815 46489816 C T 28 GENIC homozygous 54876807 6 46489905 46489906 G - 22 GENIC homozygous 54876808 6 46489926 46489927 C T 28 GENIC homozygous 54876809 6 46488137 46488138 A ACGCG 23 GENIC homozygous 55497711