chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 10067544 10067545 A G 11 GENIC homozygous 138000991 7 10067829 10067830 G A 12 GENIC homozygous 138000992 7 10068674 10068675 C T 20 GENIC homozygous 138000993 7 10068861 10068862 A C 14 GENIC homozygous 138000994 7 10069702 10069703 C G 22 GENIC homozygous 138000995 7 10071487 10071487 CATCCACCCACC 1 GENIC homozygous 137934950 7 10071687 10071688 T C 2 GENIC homozygous 138000996 7 10073090 10073091 C G 22 GENIC homozygous 138000997 7 10073320 10073321 G A 15 GENIC homozygous 138000998 7 10073635 10073636 T C 23 GENIC homozygous 138000999 7 10074103 10074104 G A 23 GENIC homozygous 138001000 7 10075796 10075796 A 12 GENIC homozygous 137934951 7 10076644 10076645 G A 19 GENIC homozygous 138001001 7 10076925 10076926 G A 20 GENIC homozygous 138001002 7 10077388 10077389 T A 15 GENIC homozygous 138001003 7 10078189 10078190 C T 19 GENIC possibly homozygous 138001004 7 10078298 10078298 CGG 3 GENIC homozygous 137934952 7 10078938 10078939 A T 25 GENIC possibly homozygous 138001005 7 10081486 10081487 G A 13 GENIC homozygous 138001006 7 10083443 10083444 C T 23 GENIC homozygous 138001007 7 10084050 10084051 C T 26 GENIC homozygous 138001008 7 10084845 10084846 C A 6 GENIC heterozygous 138001009 7 10085532 10085533 T C 5 GENIC homozygous 138001010 7 10085603 10085604 T C 6 GENIC homozygous 138001011 7 10085652 10085653 A C 14 GENIC homozygous 138001012 7 10087192 10087193 A G 18 GENIC homozygous 138001013 7 10087270 10087271 A C 21 GENIC homozygous 138001014 7 10087292 10087293 G A 24 GENIC homozygous 138001015 7 10087685 10087685 AG 9 GENIC homozygous 137934953 7 10088339 10088340 A G 19 GENIC homozygous 138001016 7 10088550 10088551 C T 10 GENIC homozygous 138001017