chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 129795360 129795361 T C 20 GENIC homozygous 574142733 7 129795406 129795407 A - 18 GENIC homozygous 714576945 7 129795959 129795960 T TTGGG 8 GENIC homozygous 714576946 7 129795961 129795962 A ATTTAGCTCAGTGGTAGAGCGCTTGCCTAG 8 GENIC homozygous 714576947 7 129796093 129796094 A T 16 GENIC homozygous 574142734 7 129796801 129796803 CC -- 11 GENIC heterozygous 714576948 7 129796802 129796803 C - 11 GENIC heterozygous 714576949 7 129797073 129797074 G A 34 GENIC homozygous 574142735 7 129798576 129798577 A AAAGC 16 GENIC homozygous 714576952 7 129798798 129798802 GAAG ---- 11 GENIC homozygous 714576954 7 129800366 129800367 T - 21 GENIC possibly homozygous 714576956 7 129800826 129800827 C CAT 2 GENIC homozygous 714576958 7 129801566 129801568 GG -- 21 GENIC heterozygous 714576959 7 129801567 129801568 G - 21 GENIC possibly homozygous 714576960 7 129802532 129802533 T C 25 GENIC homozygous 574142736 7 129803707 129803708 T A 43 GENIC homozygous 574142737 7 129803754 129803755 A C 32 GENIC homozygous 574142738 7 129804462 129804465 CAC --- 17 GENIC homozygous 714576961