chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	41033374	41033375	G	T	13	GENIC	homozygous	111550207
3	41082693	41082694	G	A	16	GENIC	homozygous	119713134
3	41082694	41082695	A	T	16	GENIC	homozygous	119713136
3	41082719	41082720	C	T	15	GENIC	homozygous	111550279
3	41082733	41082734	G	A	15	GENIC	homozygous	119713138
3	41082735	41082736	A	T	14	GENIC	homozygous	119713140
3	41083153	41083154	A	T	4	GENIC	homozygous	119884628
3	41088624	41088625	A	T	28	GENIC	homozygous	111550290
3	41088632	41088633	C	T	29	GENIC	homozygous	111903966
3	41088642	41088643	C	T	30	GENIC	homozygous	111903968
3	41088644	41088645	C	T	30	GENIC	homozygous	111903970
3	41133050	41133051	A	G	32	GENIC	heterozygous	111550345
3	41133137	41133138	G	A	33	GENIC	heterozygous	111550346
3	41133188	41133189	A	T	36	GENIC	heterozygous	111550347
3	41133199	41133200	C	T	33	GENIC	heterozygous	111550348
3	41133249	41133250	G	A	32	GENIC	heterozygous	111550349
3	41133464	41133465	T	A	37	GENIC	heterozygous	111550350
3	41133744	41133745	T	A	55	GENIC	heterozygous	111550351
3	41133921	41133922	C	T	50	GENIC	heterozygous	119893456
3	41134106	41134107	A	G	31	GENIC	heterozygous	119893457
3	41134107	41134108	T	C	31	GENIC	heterozygous	119893458
3	41134234	41134235	A	G	37	GENIC	heterozygous	111550352