chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	113910765	113910766	A	T	22	GENIC	homozygous	119651194
3	113910771	113910772	C	T	23	GENIC	homozygous	111677949
3	113917163	113917164	A	C	17	GENIC	homozygous	111677955
3	113917179	113917180	G	T	15	GENIC	homozygous	111677956
3	113917184	113917185	G	T	15	GENIC	homozygous	111677957
3	113917203	113917204	G	T	13	GENIC	homozygous	111677958
3	113917205	113917206	G	T	12	GENIC	homozygous	111677959
3	113921616	113921617	C	A	18	GENIC	homozygous	111677978
3	113921630	113921631	G	T	19	GENIC	homozygous	111677979
3	113921656	113921657	A	T	17	GENIC	homozygous	111677980
3	113921665	113921666	G	T	15	GENIC	homozygous	111677981
3	113921670	113921671	G	T	14	GENIC	homozygous	111677982
3	113921675	113921676	G	T	16	GENIC	homozygous	111677983
3	113932052	113932053	T	C	7	GENIC	homozygous	111677997
3	113932062	113932063	G	A	6	GENIC	homozygous	111677998
3	113932065	113932066	C	A	6	GENIC	homozygous	111677999
3	113951981	113951982	C	A	26	GENIC	homozygous	111678017
3	113956487	113956488	G	C	18	GENIC	homozygous	111678028