chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 43473470 43473471 C T 50 GENIC homozygous 930638776 17 43473617 43473618 G A 47 GENIC homozygous 930638777 17 43473858 43473859 C T 33 GENIC homozygous 930638778 17 43474733 43474734 G T 43 GENIC homozygous 930638779 17 43474889 43474890 G C 42 GENIC homozygous 930638780 17 43475678 43475679 G A 32 GENIC homozygous 930638781 17 43476436 43476437 T C 23 GENIC homozygous 930638782 17 43476918 43476919 T C 39 GENIC homozygous 930638783 17 43477293 43477294 G C 44 GENIC homozygous 930638784 17 43477452 43477453 G T 34 GENIC possibly homozygous 930638785 17 43479123 43479124 C T 17 GENIC homozygous 930638786 17 43479298 43479299 G A 32 GENIC homozygous 930638787 17 43479968 43479969 T A 37 GENIC homozygous 930638788 17 43481525 43481526 C A 39 GENIC homozygous 930638789 17 43482535 43482536 T C 19 GENIC homozygous 930638790 17 43484390 43484391 C G 14 GENIC homozygous 930638791 17 43486914 43486915 A G 17 GENIC homozygous 930638792 17 43489046 43489047 A G 25 GENIC homozygous 930638793 17 43489575 43489576 G T 6 GENIC homozygous 930638794 17 43489582 43489583 G T 8 GENIC homozygous 930638795 17 43490998 43490999 T C 23 GENIC homozygous 930638796 17 43491143 43491144 G T 36 GENIC homozygous 930638797 17 43493277 43493278 G A 40 GENIC homozygous 930638798 17 43493579 43493580 C T 24 GENIC homozygous 930638799 17 43495561 43495562 G C 41 GENIC homozygous 930638800 17 43495805 43495806 C T 44 GENIC homozygous 930638801 17 43496905 43496906 T C 26 GENIC homozygous 930638802 17 43497448 43497449 T G 28 GENIC homozygous 930638803 17 43500771 43500772 T A 7 GENIC homozygous 930638804