chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	1037801	1037802	T	C	3	GENIC	heterozygous	125158585
X	1042323	1042324	A	G	12	GENIC	heterozygous	125127607
X	1050398	1050399	G	C	7	GENIC	heterozygous	119899307
X	1050437	1050438	C	T	4	GENIC	heterozygous	119899308
X	1054862	1054863	A	T	9	GENIC	heterozygous	125097933
X	1057825	1057826	A	T	4	GENIC	homozygous	125158586
X	1057843	1057844	T	A	4	GENIC	heterozygous	125158587
X	1064499	1064500	T	A	7	GENIC	heterozygous	125097938
X	1064500	1064501	C	G	5	GENIC	heterozygous	125158588
X	1079301	1079302	T	A	6	GENIC	heterozygous	125147485
X	1085538	1085539	G	A	8	GENIC	homozygous	108362840
X	1096710	1096711	A	G	4	GENIC	heterozygous	125158589
X	1098305	1098306	C	T	4	GENIC	heterozygous	125158590
X	1098486	1098487	G	T	7	GENIC	heterozygous	125158591
X	1098976	1098977	G	A	40	GENIC	heterozygous	125097941
X	1098997	1098998	T	A	53	GENIC	heterozygous	125097942
X	1099021	1099022	T	A	15	GENIC	heterozygous	125097943
X	1099449	1099450	G	A	3	GENIC	heterozygous	125158592
X	1106778	1106779	A	T	6	GENIC	homozygous	108362842