chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	142284431	142284432	C	A	52	GENIC	homozygous	110038151
2	142310079	142310080	T	A	37	GENIC	homozygous	110038187
2	142315327	142315328	G	A	19	GENIC	homozygous	110038191
2	142317746	142317747	G	T	65	GENIC	homozygous	110038197
2	142317931	142317932	C	T	65	GENIC	homozygous	110038198
2	142318860	142318861	G	T	33	GENIC	homozygous	110038199
2	142318914	142318915	C	G	5	GENIC	homozygous	110594807
2	142319758	142319759	T	A	71	GENIC	possibly homozygous	110038200
2	142319798	142319799	A	C	64	GENIC	homozygous	110038202
2	142319845	142319846	A	C	78	GENIC	homozygous	110038203
2	142319939	142319940	G	T	48	GENIC	homozygous	110759384
2	142337259	142337260	T	C	52	GENIC	possibly homozygous	110038262
2	142337265	142337266	A	T	52	GENIC	homozygous	110759386
2	142337280	142337281	A	C	52	GENIC	homozygous	110038263
2	142339049	142339050	C	T	46	GENIC	homozygous	110038273
2	142339059	142339060	G	C	46	GENIC	possibly homozygous	110038274
2	142345324	142345325	C	A	58	GENIC	homozygous	110038312
2	142345445	142345446	C	A	45	GENIC	homozygous	110038313
2	142345538	142345539	A	G	41	GENIC	homozygous	110038314
2	142319349	142319350	C	G	44	GENIC	possibly homozygous	111330301
2	142434775	142434776	A	C	2	GENIC	homozygous	110759602