chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	140542995	140542995		AAA	41	GENIC	homozygous	135150884
2	140544416	140544416		T	37	GENIC	possibly homozygous	135150885
2	140544512	140544513	G		59	GENIC	homozygous	135150886
2	140543254	140543255	T	G	58	GENIC	homozygous	110035142
2	140545103	140545104	A	G	56	GENIC	homozygous	110035145
2	140544418	140544419	A	T	35	GENIC	homozygous	135157719
2	140547432	140547433	T	C	8	GENIC	homozygous	135157722
2	140545798	140545799	A	G	54	GENIC	homozygous	110035146
2	140546550	140546551	G	T	34	GENIC	homozygous	110035148
2	140545589	140545590	A	G	44	GENIC	homozygous	135157720
2	140547430	140547431	T	C	8	GENIC	homozygous	135157721
2	140547929	140547930	T		30	GENIC	homozygous	127684805
2	140546292	140546292		A	40	GENIC	heterozygous	131291150
2	140547137	140547138	T	A	41	GENIC	homozygous	120445259
2	140547641	140547642	C	T	38	GENIC	homozygous	120445260
2	140545626	140545626		T	45	GENIC	possibly homozygous	127684803
2	140548101	140548102	G	A	59	GENIC	homozygous	110035149
2	140548653	140548653		CCCCG	40	GENIC	possibly homozygous	135150887
2	140548932	140548933	T	G	66	GENIC	homozygous	110035151
2	140549496	140549497	A	G	59	GENIC	homozygous	110035152
2	140549973	140549974	A	G	63	GENIC	homozygous	120445261
2	140550130	140550130		A	66	GENIC	homozygous	127684807
2	140550131	140550132	C	A	66	GENIC	homozygous	120127220
2	140550134	140550134		A	67	GENIC	homozygous	127684808
2	140550800	140550801	C	T	57	GENIC	homozygous	110035156
2	140551269	140551270	C	G	48	GENIC	homozygous	110035157
2	140551283	140551284	C	T	55	GENIC	homozygous	110035159
2	140551310	140551311	C	G	58	GENIC	homozygous	110035160
2	140551563	140551564	T	C	68	GENIC	homozygous	110035164
2	140552190	140552191	A	G	65	GENIC	homozygous	110035165