chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 90958090 90958091 A AG 25 GENIC homozygous 712996749 10 90960440 90960441 C T 32 GENIC homozygous 573535577 10 90963310 90963311 G C 41 GENIC homozygous 575288313 10 90963374 90963375 G C 48 GENIC homozygous 573535578 10 90964012 90964016 AAAA ---- 37 GENIC homozygous 712996750 10 90964015 90964016 A AGTG 22 GENIC homozygous 712996751 10 90964017 90964018 A T 35 GENIC homozygous 575288314 10 90964062 90964063 T G 36 GENIC homozygous 573535579 10 90965013 90965014 C CTGTGTG 10 GENIC heterozygous 712996755 10 90965013 90965014 C CTGTGTGTG 10 GENIC possibly homozygous 712996756 10 90965092 90965093 G A 28 GENIC homozygous 575288315 10 90965149 90965150 T C 42 GENIC homozygous 573535580 10 90965236 90965240 TTGT ---- 18 GENIC homozygous 712996757 10 90965577 90965578 T TCA 19 GENIC homozygous 712996758 10 90965616 90965617 T TACACACACACACACACACAC 19 GENIC homozygous 712996761 10 90966365 90966366 G GT 4 GENIC homozygous 712996763 10 90966431 90966432 C CT 1 GENIC homozygous 712996764 10 90966997 90966998 A - 19 GENIC homozygous 712996767 10 90967787 90967788 G A 28 GENIC homozygous 573535581 10 90967887 90967888 T C 32 GENIC homozygous 575288316 10 90967951 90967952 T G 35 GENIC homozygous 573535582 10 90968077 90968078 A G 30 GENIC homozygous 573535583