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	10	GENIC	homozygous	108704044
X	40263902	40263903	C	A	8	GENIC	homozygous	108482617
X	40265084	40265085	A	G	6	GENIC	homozygous	108482619
X	40269611	40269612	C	G	13	GENIC	homozygous	108482623
X	40272345	40272346	G	A	9	GENIC	heterozygous	125130082
X	40272565	40272566	T	C	9	GENIC	homozygous	108482625
X	40276638	40276639	G	T	9	GENIC	homozygous	108482627
X	40278083	40278084	G	A	10	GENIC	homozygous	108704046
X	40280263	40280264	T	C	5	GENIC	homozygous	108482629
X	40280266	40280267	T	C	6	GENIC	homozygous	108482631
X	40280272	40280273	C	T	8	GENIC	homozygous	108482633
X	40284071	40284072	T	C	4	GENIC	homozygous	108566699
X	40267071	40267072	C	T	3	GENIC	heterozygous	125104007
X	40279876	40279877	G	C	6	GENIC	homozygous	125104008
X	40276203	40276204	T	C	12	GENIC	homozygous	108566695
X	40280340	40280341	G	A	4	GENIC	heterozygous	125161377
X	40286611	40286612	C	T	6	GENIC	homozygous	108704052
X	40289094	40289095	G	A	8	GENIC	homozygous	108482637
X	40292354	40292355	T	G	6	GENIC	homozygous	108256728
X	40292360	40292361	G	C	6	GENIC	homozygous	108256730
X	40292473	40292474	A	G	5	GENIC	homozygous	108256732
X	40293050	40293051	C	G	14	GENIC	homozygous	108482644
X	40295314	40295315	T	C	12	GENIC	homozygous	108704054
X	40296145	40296146	T	C	11	GENIC	homozygous	108482646
X	40304614	40304615	G	T	11	GENIC	heterozygous	120585377
X	40307676	40307677	C	G	5	GENIC	homozygous	108482662
X	40307704	40307705	A	T	6	GENIC	homozygous	108482664