chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 170364426 170364427 G A 45 GENIC homozygous 112371076 3 170365122 170365123 G 40 GENIC homozygous 127959696 3 170365980 170365981 A G 54 GENIC homozygous 111834356 3 170366006 170366007 T A 55 GENIC homozygous 111834358 3 170366984 170366985 G T 62 GENIC homozygous 112203739 3 170367168 170367171 CCA 44 GENIC homozygous 127959697 3 170367205 170367206 G C 56 GENIC homozygous 112371077 3 170367605 170367605 C 39 GENIC homozygous 127959698 3 170367703 170367704 T A 54 GENIC possibly homozygous 111834364 3 170367852 170367853 G A 52 GENIC homozygous 111834366 3 170369149 170369150 T C 49 GENIC homozygous 111834368 3 170369419 170369419 GGACACACAGGGCAGGAGCTGGGAGAGGGAGAATTCAGACTGGGAGGAGACACCTGCAGGAA 25 GENIC homozygous 127959699 3 170370834 170370835 C G 40 GENIC homozygous 111834376 3 170371347 170371348 A G 49 GENIC homozygous 111834378 3 170371396 170371397 T C 51 GENIC homozygous 111834380 3 170371669 170371670 G A 40 GENIC homozygous 112371078 3 170372273 170372274 A G 65 GENIC homozygous 111834382 3 170373273 170373274 A G 37 GENIC homozygous 111834384 3 170374367 170374368 A C 40 GENIC homozygous 111834388 3 170375409 170375410 T C 48 GENIC homozygous 111834390 3 170375495 170375496 A T 32 GENIC possibly homozygous 112371079 3 170377719 170377720 A G 58 GENIC homozygous 111834394 3 170377908 170377909 G A 26 GENIC homozygous 112203765 3 170379107 170379107 T 35 GENIC homozygous 127959701 3 170379541 170379542 C T 46 GENIC homozygous 112371080 3 170379834 170379835 G A 42 GENIC homozygous 111834398