chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 59587110 59587111 C T 16 GENIC possibly homozygous 51465833 10 59587832 59587833 G C 21 GENIC possibly homozygous 52562746 10 59588086 59588087 G A 27 GENIC possibly homozygous 52562749 10 59589767 59589768 T C 16 GENIC homozygous 51465835 10 59591293 59591300 GGCATTT ------- 6 GENIC homozygous 51465836 10 59593907 59593908 T C 36 GENIC homozygous 51465837 10 59596666 59596667 C T 17 GENIC possibly homozygous 52562752 10 59596806 59596807 G A 20 GENIC homozygous 51663693 10 59596958 59596959 T C 19 GENIC possibly homozygous 51663695 10 59597018 59597019 T A 13 GENIC homozygous 51663697 10 59597105 59597106 G GC 8 GENIC heterozygous 51465838 10 59598261 59598262 T TATC 5 GENIC homozygous 51663705 10 59599284 59599285 G T 27 GENIC possibly homozygous 51465839 10 59600128 59600129 G - 11 GENIC possibly homozygous 51465841 10 59603914 59603915 C A 23 GENIC homozygous 52562755 10 59605540 59605541 T C 15 GENIC possibly homozygous 52562758 10 59606197 59606198 G A 18 GENIC possibly homozygous 52562761 10 59606336 59606337 A G 24 GENIC homozygous 51663721 10 59606505 59606506 C T 22 GENIC possibly homozygous 51465846