chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 102136316 102136317 G - 22 GENIC homozygous 51587352 10 102137007 102137008 T C 25 GENIC homozygous 51587354 10 102137511 102137512 A G 36 GENIC homozygous 51587356 10 102137788 102137789 G A 24 GENIC homozygous 51587358 10 102137857 102137858 T C 27 GENIC homozygous 51587360 10 102137865 102137866 A G 26 GENIC homozygous 51587362 10 102138327 102138328 A G 29 GENIC homozygous 51587364 10 102139127 102139128 G A 26 GENIC possibly homozygous 51587366 10 102139449 102139450 T C 35 GENIC homozygous 51587368 10 102139634 102139635 A T 21 GENIC homozygous 51587370 10 102139657 102139660 TTT --- 17 GENIC possibly homozygous 51587372 10 102139666 102139669 TTC --- 20 GENIC homozygous 51587374 10 102139770 102139771 C T 18 GENIC homozygous 51587376 10 102140038 102140039 C T 21 GENIC homozygous 51587378 10 102140505 102140506 T C 13 GENIC homozygous 51587380 10 102141647 102141648 A G 24 GENIC homozygous 51587382 10 102141652 102141653 A G 24 GENIC homozygous 51587384 10 102141692 102141693 C A 32 GENIC homozygous 51587386 10 102141972 102141973 T - 20 GENIC homozygous 51587388 10 102142112 102142113 T TG 27 GENIC homozygous 51587390 10 102142276 102142277 T C 29 GENIC homozygous 51587392 10 102143189 102143190 C CAAAA 4 GENIC heterozygous 51587394 10 102143189 102143190 C CAAA 4 GENIC heterozygous 51587396