chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	141146619	141146620	T	C	21	GENIC	homozygous	63020803
X	141151522	141151523	A	T	20	GENIC	homozygous	63020805
X	141152219	141152220	G	A	24	GENIC	homozygous	63020806
X	141152310	141152311	G	A	13	GENIC	heterozygous	63020807
X	141152522	141152523	C	T	14	GENIC	homozygous	63020808
X	141152532	141152533	A	G	13	GENIC	homozygous	63020809
X	141153364	141153365	A	G	22	GENIC	homozygous	63020810
X	141153837	141153838	C	T	10	GENIC	homozygous	63020811
X	141154986	141154987	C	T	21	GENIC	homozygous	63020812
X	141155654	141155655	G	A	17	GENIC	homozygous	63020813
X	141156619	141156620	C	T	12	GENIC	homozygous	63020814
X	141157229	141157230	C	T	22	GENIC	homozygous	63020815
X	141161179	141161180	G	A	9	GENIC	homozygous	63020816
X	141162782	141162783	A	G	10	GENIC	homozygous	63020817
X	141164476	141164477	G	A	16	GENIC	homozygous	63020818
X	141164873	141164874	T	A	9	GENIC	homozygous	63020819
X	141165066	141165067	G	T	11	GENIC	homozygous	63020820
X	141165803	141165804	T	C	18	GENIC	homozygous	63020821
X	141165889	141165890	A	G	19	GENIC	homozygous	63020822
X	141178511	141178512	C	T	13	GENIC	homozygous	63020823
X	141178918	141178919	C	T	13	GENIC	homozygous	63020824
X	141180550	141180551	G	A	17	GENIC	homozygous	63020825
X	141182220	141182221	T	C	11	GENIC	homozygous	63020829
X	141182290	141182291	C	T	12	GENIC	homozygous	63020830
X	141182840	141182841	C	A	14	GENIC	homozygous	63020831
X	141182955	141182956	C	T	29	GENIC	homozygous	63020832
X	141183045	141183046	C	T	20	GENIC	possibly homozygous	63020833
X	141183158	141183159	G	T	18	GENIC	homozygous	63020834
X	141183514	141183515	A	G	11	GENIC	homozygous	63020835
X	141184001	141184002	A	G	19	GENIC	homozygous	63020836
X	141185009	141185010	T	C	9	GENIC	homozygous	63020837
X	141185119	141185120	C	G	8	GENIC	homozygous	63020838
X	141196494	141196495	C	T	14	GENIC	homozygous	63020841
X	141200959	141200960	A	C	26	GENIC	homozygous	63020842