chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 227052063 227052064 G T 26 GENIC homozygous 581168612 1 227052132 227052133 A G 18 GENIC possibly homozygous 581168613 1 227052161 227052162 T C 17 GENIC heterozygous 581168614 1 227052456 227052457 A G 6 GENIC heterozygous 581168615 1 227053226 227053227 T G 11 GENIC heterozygous 581168616 1 227053481 227053482 T C 29 GENIC homozygous 581168617 1 227054276 227054277 A G 19 GENIC homozygous 581168618 1 227054307 227054308 T C 13 GENIC homozygous 581168619 1 227054702 227054703 C A 16 GENIC homozygous 581168620 1 227054824 227054825 T - 6 GENIC homozygous 716942983 1 227054848 227054849 T - 5 GENIC heterozygous 716942984 1 227054862 227054863 C T 10 GENIC homozygous 581168621 1 227056560 227056561 C T 15 GENIC possibly homozygous 581168622 1 227056646 227056647 A G 8 GENIC heterozygous 581168623 1 227056865 227056866 C T 1 GENIC homozygous 581168624 1 227057105 227057106 C CT 3 GENIC heterozygous 716942985 1 227057578 227057579 C G 8 GENIC homozygous 581168625 1 227059813 227059814 C T 5 GENIC heterozygous 581168626 1 227060252 227060253 G A 21 GENIC homozygous 581168627 1 227060697 227060698 C A 15 GENIC homozygous 581168628 1 227060713 227060714 G T 14 GENIC homozygous 581168629 1 227060832 227060833 G C 13 GENIC heterozygous 581168630 1 227060931 227060932 T C 17 GENIC possibly homozygous 581168631 1 227061388 227061389 A G 5 GENIC homozygous 581168632 1 227061763 227061764 T C 27 GENIC possibly homozygous 581168633 1 227062085 227062086 T TG 19 GENIC possibly homozygous 716942987 1 227062103 227062104 G A 23 GENIC homozygous 581168634 1 227065309 227065310 G C 19 GENIC homozygous 581168635 1 227065396 227065397 A T 8 GENIC heterozygous 581168636 1 227066147 227066148 T C 20 GENIC homozygous 581168637 1 227066210 227066212 GG -- 3 GENIC homozygous 716942988 1 227067008 227067009 C A 14 GENIC homozygous 581168638