chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	116089085	116089086	G	A	10	GENIC	homozygous	143725286
X	116090391	116090392	G	A	4	GENIC	homozygous	140688010
X	116091135	116091136	G	A	9	GENIC	homozygous	143725287
X	116092156	116092157	C	A	5	GENIC	homozygous	140688012
X	116092661	116092662	C	A	3	GENIC	homozygous	143725288
X	116093595	116093596	G	C	13	GENIC	homozygous	140688013
X	116093745	116093746	G	A	9	GENIC	homozygous	143725289
X	116094934	116094935	G	A	11	GENIC	homozygous	144219942
X	116096050	116096051	T	C	9	GENIC	homozygous	140688014
X	116098856	116098861	ATAGT		9	GENIC	homozygous	143723053
X	116099364	116099365	G	T	8	GENIC	homozygous	140688015
X	116102730	116102731	T		7	GENIC	possibly homozygous	403487180
X	116102732	116102733	T		7	GENIC	possibly homozygous	403487182
X	116102728	116102729	T		7	GENIC	possibly homozygous	403487178
X	116102728	116102729	T	A	7	GENIC	heterozygous	403487179
X	116102730	116102731	T	A	7	GENIC	heterozygous	403487181
X	116102732	116102733	T	A	7	GENIC	heterozygous	403487183
X	116102734	116102735	T	A	7	GENIC	heterozygous	403487184
X	116102734	116102735	T		7	GENIC	possibly homozygous	403487185
X	116102738	116102739	T		7	GENIC	possibly homozygous	403487186
X	116102738	116102739	T	A	7	GENIC	heterozygous	403487187
X	116103463	116103464	A		6	GENIC	homozygous	140593766
X	116106050	116106051	T	C	8	GENIC	homozygous	140688016
X	116108364	116108364		T	6	GENIC	homozygous	140593767
X	116111534	116111535	A	G	12	GENIC	homozygous	143725290
X	116113134	116113135	C	T	10	GENIC	homozygous	140688018