chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 61361934 61361935 C CTGGTATA 23 GENIC heterozygous 52908834 9 61363109 61363110 C T 14 GENIC homozygous 51992746 9 61362462 61362463 G GA 12 GENIC homozygous 51992738 9 61362666 61362667 T C 11 GENIC homozygous 51992741 9 61363036 61363038 GC -- 10 GENIC homozygous 51992744 9 61363165 61363166 G A 11 GENIC homozygous 51992749 9 61363467 61363468 T G 18 GENIC homozygous 51992758 9 61364281 61364282 A G 24 GENIC homozygous 51992761 9 61364344 61364345 T G 24 GENIC homozygous 51992764 9 61364757 61364758 T C 27 GENIC homozygous 51992767 9 61364918 61364919 G A 21 GENIC homozygous 51992770 9 61365041 61365042 C T 30 GENIC homozygous 51992773 9 61368757 61368758 C T 37 GENIC homozygous 51992776 9 61368853 61368854 A G 22 GENIC homozygous 51992779 9 61369374 61369375 C CA 18 GENIC possibly homozygous 51992786 9 61366871 61366872 G GTGAGACCCTGTCTCAAAAACATGACTACACAA 22 GENIC homozygous 52855620