chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 97047346 97047347 A - 13 GENIC homozygous 52064990 9 97047539 97047540 T C 19 GENIC homozygous 52064992 9 97048006 97048007 C T 30 GENIC homozygous 52064994 9 97048301 97048302 A C 40 GENIC homozygous 52064996 9 97049556 97049557 G T 29 GENIC homozygous 52064998 9 97049796 97049797 G A 45 GENIC homozygous 52065000 9 97050354 97050355 G A 37 GENIC possibly homozygous 52065002 9 97051462 97051463 G A 35 GENIC homozygous 52065004 9 97051672 97051673 T C 54 GENIC homozygous 52065005 9 97052214 97052215 G A 39 GENIC homozygous 52065007 9 97052570 97052571 T A 33 GENIC possibly homozygous 52065010 9 97054399 97054400 G GTGTC 11 GENIC heterozygous 52065012 9 97054399 97054400 G GTGTGTC 11 GENIC heterozygous 52065014 9 97054854 97054855 T C 31 GENIC homozygous 52065016 9 97055128 97055129 G C 27 GENIC homozygous 52065018 9 97055222 97055223 C - 33 GENIC homozygous 52065020 9 97055403 97055404 A G 30 GENIC homozygous 52065022 9 97055498 97055500 GG -- 26 GENIC homozygous 52065024 9 97055910 97055915 CATGG ----- 27 GENIC homozygous 52065026 9 97056241 97056242 A G 31 GENIC homozygous 52065028 9 97057671 97057672 T C 38 GENIC homozygous 52065030 9 97058332 97058333 C T 19 GENIC homozygous 52065032 9 97054399 97054400 G C 24 GENIC heterozygous 52282869