chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 40518598 40518599 T C 29 GENIC homozygous 52593154 8 40518628 40518629 A G 27 GENIC homozygous 52964367 8 40518631 40518632 G C 27 GENIC homozygous 52593155 8 40518635 40518636 A C 26 GENIC homozygous 52593156 8 40518688 40518689 T C 33 GENIC heterozygous 52593158 8 40518694 40518695 C A 38 GENIC heterozygous 52593159 8 40518697 40518698 G A 41 GENIC heterozygous 52593160 8 40518700 40518701 T C 44 GENIC heterozygous 52593161 8 40518701 40518702 A G 45 GENIC heterozygous 52593162 8 40518717 40518718 A G 62 GENIC heterozygous 52964368 8 40518745 40518746 C T 86 GENIC heterozygous 52964369 8 40518781 40518782 C T 103 GENIC heterozygous 53203414 8 40518785 40518786 A T 98 GENIC heterozygous 53203415 8 40518795 40518796 C T 98 GENIC heterozygous 52964370 8 40518839 40518840 C T 57 GENIC heterozygous 52964371 8 40518847 40518848 G A 54 GENIC heterozygous 52593166 8 40518857 40518858 C - 32 GENIC heterozygous 52964372 8 40518877 40518878 T C 41 GENIC heterozygous 52964373 8 40518898 40518899 C T 32 GENIC heterozygous 52593169 8 40518902 40518903 C T 31 GENIC heterozygous 52593170 8 40519063 40519064 T C 33 GENIC possibly homozygous 52593171 8 40519279 40519280 C G 30 GENIC possibly homozygous 52964374 8 40519372 40519373 A T 24 GENIC homozygous 52964375