chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 196607156 196607157 A G 20 GENIC homozygous 110196087 2 196607918 196607918 A 22 GENIC homozygous 127722639 2 196607942 196607943 C 20 GENIC homozygous 127722640 2 196607950 196607950 C 24 GENIC homozygous 127722641 2 196607960 196607960 T 25 GENIC homozygous 127722642 2 196607964 196607964 C 24 GENIC homozygous 127722643 2 196607970 196607970 A 27 GENIC homozygous 127722644 2 196608048 196608049 A 27 GENIC homozygous 127722645 2 196608054 196608054 A 26 GENIC homozygous 127722646 2 196608093 196608094 T 6 GENIC homozygous 127722647 2 196609411 196609412 T C 13 GENIC homozygous 110196089 2 196612473 196612477 TCTG 18 GENIC homozygous 127722648 2 196619074 196619075 C T 15 GENIC homozygous 110196090 2 196623438 196623439 G A 14 GENIC homozygous 110196091 2 196643866 196643867 C T 8 GENIC homozygous 110196094 2 196648282 196648283 G A 20 GENIC possibly homozygous 110196095 2 196651443 196651444 G A 5 GENIC homozygous 110196096 2 196648600 196648603 TGA 13 GENIC homozygous 127722653 2 196628341 196628342 C T 7 GENIC homozygous 127831290