chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 143820831 143820832 A G 23 GENIC homozygous 115944684 7 143820870 143820871 G T 27 GENIC homozygous 116100797 7 143823699 143823700 A G 25 GENIC homozygous 115944685 7 143826120 143826121 G T 35 GENIC homozygous 115944687 7 143826140 143826141 C T 32 GENIC homozygous 116100799 7 143826854 143826855 G A 25 GENIC homozygous 115944688 7 143827261 143827262 A G 18 GENIC homozygous 115944690 7 143828599 143828600 G A 32 GENIC homozygous 115944691 7 143829200 143829201 G A 29 GENIC possibly homozygous 115944692 7 143829430 143829431 A G 21 GENIC homozygous 116100801 7 143829503 143829504 G A 20 GENIC possibly homozygous 116100803 7 143829736 143829737 A G 10 GENIC homozygous 115944693 7 143829920 143829921 G A 26 GENIC heterozygous 115944697 7 143829924 143829925 G A 25 GENIC heterozygous 115944698 7 143830114 143830115 T C 24 GENIC homozygous 115944701 7 143830866 143830867 G A 26 GENIC homozygous 115944703 7 143832105 143832106 T C 28 GENIC heterozygous 116100807 7 143836286 143836287 C A 14 GENIC homozygous 116100809 7 143836445 143836446 C T 28 GENIC homozygous 116100811 7 143836849 143836850 G A 30 GENIC homozygous 116100813