chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 11462277 11462278 T G 29 GENIC homozygous 110957768 17 11462986 11462987 T C 4 GENIC homozygous 111557951 17 11462992 11462993 G C 2 GENIC homozygous 111557953 17 11464855 11464856 C T 24 GENIC homozygous 110957770 17 11465381 11465382 G A 34 GENIC possibly homozygous 110957774 17 11468231 11468232 T C 23 GENIC homozygous 110957782 17 11468436 11468437 T G 11 GENIC homozygous 110957784 17 11468540 11468541 G A 13 GENIC homozygous 110957786 17 11468851 11468852 T C 15 GENIC homozygous 110957789 17 11469260 11469261 G A 20 GENIC homozygous 110957791 17 11469792 11469793 G A 7 GENIC homozygous 110957793 17 11470007 11470008 G A 6 GENIC homozygous 111412950 17 11470008 11470009 A G 6 GENIC homozygous 111381229 17 11470407 11470408 T C 17 GENIC homozygous 110957795 17 11470661 11470662 G A 19 GENIC possibly homozygous 110957797 17 11470786 11470787 G A 13 GENIC homozygous 110957799 17 11470812 11470813 T C 13 GENIC homozygous 110957801 17 11470862 11470863 G A 18 GENIC homozygous 110957803 17 11470943 11470944 T C 14 GENIC homozygous 110957806 17 11472172 11472173 A G 17 GENIC homozygous 110957808 17 11473065 11473066 C T 15 GENIC homozygous 110957810 17 11473076 11473077 C G 16 GENIC possibly homozygous 110957812 17 11473663 11473664 A G 6 GENIC homozygous 110957814 17 11474475 11474476 C T 12 GENIC homozygous 110957816 17 11470018 11470019 T C 5 GENIC homozygous 111495754