chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	122194745	122194746	C	T	54	GENIC	homozygous	111690175
3	122195519	122195520	A	G	42	GENIC	homozygous	111690176
3	122195603	122195604	A	G	47	GENIC	homozygous	111690177
3	122196187	122196188	C	T	38	GENIC	homozygous	112146814
3	122196249	122196250	T	G	46	GENIC	homozygous	111690178
3	122196479	122196480	C	T	39	GENIC	homozygous	111690179
3	122197178	122197179	G	A	45	GENIC	homozygous	111690180
3	122197578	122197579	T	C	44	GENIC	homozygous	111690181
3	122197583	122197584	T	C	47	GENIC	homozygous	111690182
3	122198210	122198211	G	A	43	GENIC	homozygous	111690183
3	122198281	122198282	A	G	44	GENIC	homozygous	111690184
3	122198340	122198341	T	C	40	GENIC	homozygous	112146815
3	122199716	122199717	C	T	55	GENIC	homozygous	112146817
3	122199905	122199906	C	T	51	GENIC	homozygous	111690185
3	122201826	122201827	T	C	59	GENIC	homozygous	112146819
3	122201835	122201836	A	G	59	GENIC	homozygous	111690186
3	122202770	122202771	T	C	39	GENIC	homozygous	111690187
3	122203340	122203341	C	T	60	GENIC	homozygous	112146821
3	122204686	122204687	G	A	48	GENIC	homozygous	111690188
3	122205159	122205160	C	G	40	GENIC	homozygous	111690190
3	122205402	122205403	G	C	40	GENIC	homozygous	119651398
3	122205452	122205453	A	G	40	GENIC	homozygous	111690191
3	122205933	122205934	C	G	34	GENIC	homozygous	111690192
3	122206045	122206046	G	A	49	GENIC	homozygous	112146823
3	122206279	122206280	A	G	42	GENIC	homozygous	111690193
3	122200110	122200110		TT	38	GENIC	homozygous	127924938
3	122202420	122202420		TGAT	28	GENIC	homozygous	127924939
3	122205400	122205401	A		40	GENIC	homozygous	127924940