chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	105239745	105239746	T	A	13	GENIC	homozygous	108527776
X	105240923	105240924	C	T	14	GENIC	homozygous	108733561
X	105241487	105241488	A	G	14	GENIC	homozygous	108527778
X	105242495	105242496	C	T	14	GENIC	homozygous	108527780
X	105242663	105242664	A	G	15	GENIC	homozygous	108527782
X	105243192	105243193	C	T	18	GENIC	homozygous	108527787
X	105243688	105243689	A	G	26	GENIC	homozygous	108733563
X	105243873	105243874	C	A	3	GENIC	homozygous	108733565
X	105247539	105247540	C	G	18	GENIC	homozygous	108527789
X	105250392	105250393	C	T	14	GENIC	homozygous	108733567
X	105251538	105251539	G	A	20	GENIC	homozygous	108527794
X	105251573	105251574	A	G	16	GENIC	homozygous	108527796
X	105252235	105252236	T	G	6	GENIC	homozygous	108733569
X	105252292	105252293	G	A	6	GENIC	homozygous	108527798
X	105253197	105253198	A	T	18	GENIC	homozygous	108527800
X	105256765	105256766	T	C	19	GENIC	homozygous	108733571
X	105258722	105258723	A	G	16	GENIC	homozygous	108733573
X	105259002	105259003	A	C	18	GENIC	homozygous	108733575
X	105260429	105260430	A	G	28	GENIC	homozygous	108667532
X	105261913	105261914	C	T	21	GENIC	homozygous	108667534
X	105262105	105262106	A	G	7	GENIC	homozygous	108667536
X	105264448	105264449	G	A	15	GENIC	homozygous	108733577
X	105265399	105265400	G	A	25	GENIC	homozygous	108667540
X	105265514	105265515	G	A	7	GENIC	homozygous	108733579
X	105266847	105266848	T	A	15	GENIC	homozygous	108527818
X	105267123	105267124	A	G	6	GENIC	homozygous	108527820
X	105271034	105271035	A	G	21	GENIC	homozygous	108527822
X	105274274	105274275	C	T	9	GENIC	homozygous	108527824
X	105274307	105274308	T	C	14	GENIC	homozygous	108527826
X	105275091	105275092	C	T	25	GENIC	homozygous	108527828
X	105277615	105277616	T	A	11	GENIC	homozygous	108733581
X	105280818	105280819	C	A	15	GENIC	homozygous	108733583
X	105289415	105289416	T	C	4	GENIC	homozygous	108527838
X	105289441	105289442	T	C	4	GENIC	homozygous	108527840