chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 137148586 137148587 C T 10 GENIC homozygous 822834907 7 137148798 137148799 A G 8 GENIC homozygous 822834908 7 137148956 137148957 T A 10 GENIC homozygous 822834909 7 137149347 137149349 AA -- 8 GENIC homozygous 822834910 7 137149410 137149411 A T 13 GENIC homozygous 822834911 7 137149534 137149535 G A 18 GENIC homozygous 822834912 7 137149644 137149645 G A 11 GENIC homozygous 822834913 7 137149935 137149936 A T 15 GENIC homozygous 822834914 7 137149997 137149998 C CTTGTTTGT 13 GENIC homozygous 822834915 7 137150134 137150135 T - 19 GENIC homozygous 822834916 7 137150351 137150352 A G 17 GENIC homozygous 822834917 7 137151268 137151269 G A 13 GENIC homozygous 822834918 7 137151311 137151312 G GTGTC 8 GENIC homozygous 822834919 7 137151732 137151733 G A 10 GENIC homozygous 822834920 7 137152162 137152163 T C 8 GENIC homozygous 822834921 7 137152728 137152729 A G 14 GENIC homozygous 822834922 7 137152946 137152947 A G 15 GENIC homozygous 822834923 7 137153127 137153128 G A 13 GENIC homozygous 822834924 7 137153658 137153659 C A 17 GENIC homozygous 822834925 7 137153697 137153698 T A 14 GENIC homozygous 822834926 7 137153848 137153849 G A 12 GENIC homozygous 822834927 7 137154398 137154399 C T 12 GENIC homozygous 822834928 7 137154438 137154439 T G 19 GENIC homozygous 822834929