chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	40259790	40259791	G	A	11	GENIC	homozygous	108482613
X	40263728	40263729	C	G	16	GENIC	homozygous	108704044
X	40263902	40263903	C	A	14	GENIC	homozygous	108482617
X	40265084	40265085	A	G	12	GENIC	homozygous	108482619
X	40269611	40269612	C	G	7	GENIC	homozygous	108482623
X	40272565	40272566	T	C	11	GENIC	homozygous	108482625
X	40276638	40276639	G	T	15	GENIC	homozygous	108482627
X	40278083	40278084	G	A	16	GENIC	homozygous	108704046
X	40280136	40280137	C	A	12	GENIC	homozygous	108704048
X	40280263	40280264	T	C	8	GENIC	homozygous	108482629
X	40280266	40280267	T	C	8	GENIC	homozygous	108482631
X	40280272	40280273	C	T	7	GENIC	homozygous	108482633
X	40281372	40281373	G	T	13	GENIC	homozygous	108525198
X	40283974	40283975	C	T	5	GENIC	homozygous	108704050
X	40286611	40286612	C	T	11	GENIC	homozygous	108704052
X	40289094	40289095	G	A	9	GENIC	homozygous	108482637
X	40292279	40292280	T	C	9	GENIC	homozygous	108256716
X	40292280	40292281	A	T	9	GENIC	homozygous	108256718
X	40292282	40292283	A	C	9	GENIC	homozygous	108256720
X	40292302	40292303	A	T	10	GENIC	homozygous	108256722
X	40292303	40292304	G	A	10	GENIC	homozygous	108256724
X	40292307	40292308	C	G	10	GENIC	homozygous	108256726
X	40292354	40292355	T	G	13	GENIC	homozygous	108256728
X	40292360	40292361	G	C	14	GENIC	homozygous	108256730
X	40292473	40292474	A	G	13	GENIC	homozygous	108256732
X	40295314	40295315	T	C	13	GENIC	homozygous	108704054
X	40296145	40296146	T	C	10	GENIC	homozygous	108482646
X	40307676	40307677	C	G	10	GENIC	homozygous	108482662
X	40307704	40307705	A	T	9	GENIC	homozygous	108482664