chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 47400244 47400245 T C 72 GENIC homozygous 116773595 10 47401181 47401182 T C 39 GENIC homozygous 116773597 10 47402668 47402669 T G 54 GENIC homozygous 116773599 10 47402874 47402875 T C 58 GENIC homozygous 116773601 10 47401387 47401388 G C 23 GENIC homozygous 117008804 10 47401415 47401416 A G 23 GENIC homozygous 118036496 10 47403590 47403591 T C 23 GENIC heterozygous 117218325 10 47401470 47401473 TGG 44 GENIC homozygous 133228307 10 47404637 47404641 CTAT 54 GENIC possibly homozygous 133228308 10 47403591 47403592 G A 23 GENIC heterozygous 131905502 10 47404943 47404944 A G 51 GENIC homozygous 116773603 10 47406814 47406815 T C 48 GENIC homozygous 116773607 10 47408000 47408001 A 43 GENIC homozygous 133228309 10 47408806 47408807 A G 43 GENIC homozygous 116773609 10 47408963 47408963 AGGC 29 GENIC homozygous 132691672 10 47409089 47409090 A G 53 GENIC homozygous 116773611 10 47409136 47409137 G A 60 GENIC homozygous 116773613 10 47409253 47409253 T 70 GENIC possibly homozygous 132691673 10 47409615 47409616 A G 56 GENIC homozygous 116773615 10 47409675 47409676 G C 48 GENIC homozygous 116773617 10 47415354 47415355 G 10 GENIC homozygous 133228310 10 47419071 47419072 G A 60 GENIC homozygous 116773635 10 47414239 47414240 A G 54 GENIC homozygous 116773619 10 47415810 47415811 A G 50 GENIC homozygous 116773621 10 47416185 47416186 G A 47 GENIC homozygous 116773623 10 47416375 47416376 A G 59 GENIC homozygous 116773625 10 47417103 47417104 T C 60 GENIC homozygous 116773627 10 47418081 47418082 A G 55 GENIC homozygous 116773629 10 47418273 47418274 C T 55 GENIC homozygous 116773631 10 47419282 47419283 A G 37 GENIC homozygous 116773637 10 47419350 47419351 C T 52 GENIC homozygous 116878587 10 47420921 47420922 G A 47 GENIC homozygous 117008805 10 47422763 47422764 T C 51 GENIC homozygous 116878589