chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 129795360 129795361 T C 3 GENIC homozygous 614687928 7 129795406 129795407 A - 17 GENIC possibly homozygous 737649903 7 129795959 129795960 T TTGGG 1 GENIC homozygous 737649904 7 129795961 129795962 A ATTTAGCTCAGTGGTAGAGCGCTTGCCTAG 1 GENIC homozygous 737649905 7 129796093 129796094 A T 26 GENIC homozygous 614687929 7 129796800 129796803 ACC --- 9 GENIC heterozygous 737649906 7 129796801 129796803 CC -- 9 GENIC heterozygous 737649907 7 129796802 129796803 C - 9 GENIC heterozygous 737649908 7 129797073 129797074 G A 27 GENIC homozygous 614687930 7 129798576 129798577 A AAAGC 5 GENIC homozygous 737649911 7 129799664 129799665 C T 30 GENIC homozygous 615234843 7 129800366 129800367 T - 19 GENIC homozygous 737649912 7 129800826 129800827 C CAT 21 GENIC homozygous 737649914 7 129801566 129801568 GG -- 8 GENIC heterozygous 737649915 7 129801567 129801568 G - 8 GENIC possibly homozygous 737649916 7 129802532 129802533 T C 23 GENIC homozygous 614687931 7 129803707 129803708 T A 33 GENIC homozygous 614687932 7 129803754 129803755 A C 22 GENIC homozygous 614687933 7 129804462 129804465 CAC --- 13 GENIC homozygous 737649917