chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 70507879 70507880 T G 46 GENIC homozygous 137079394 4 70508978 70508979 G A 62 GENIC homozygous 137079395 4 70511263 70511264 A 13 GENIC heterozygous 403102991 4 70511263 70511264 A G 13 GENIC heterozygous 403102992 4 70512697 70512698 C T 52 GENIC homozygous 137079396 4 70513072 70513073 G T 41 GENIC homozygous 137079397 4 70513237 70513238 G 14 GENIC heterozygous 403102993 4 70513317 70513318 C G 40 GENIC homozygous 137079398 4 70513648 70513649 C T 50 GENIC homozygous 137079399 4 70514912 70514913 C T 56 GENIC homozygous 137079400 4 70515833 70515834 A T 68 GENIC homozygous 137079401 4 70515996 70515997 C T 43 GENIC homozygous 137079402 4 70516294 70516295 G A 56 GENIC homozygous 137079403 4 70516446 70516447 C T 50 GENIC homozygous 137079404 4 70516606 70516607 C T 45 GENIC homozygous 137079405 4 70517136 70517137 T 39 GENIC possibly homozygous 403102994 4 70517136 70517137 T C 39 GENIC heterozygous 403102995 4 70517583 70517584 T C 51 GENIC homozygous 137079406 4 70517754 70517755 C A 79 GENIC homozygous 137079407 4 70517816 70517817 G A 72 GENIC homozygous 137079408 4 70519721 70519722 A G 52 GENIC homozygous 137079409 4 70513237 70513238 G A 14 GENIC possibly homozygous 140878406 4 70513228 70513230 AA 29 GENIC possibly homozygous 136891134 4 70522164 70522164 T 60 GENIC homozygous 136891135