chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	236048238	236048239	C	T	22	GENIC	homozygous	110318136
2	236048248	236048249	T	C	25	GENIC	homozygous	110318138
2	236048273	236048274	T	C	27	GENIC	homozygous	110318140
2	236048328	236048329	C	G	26	GENIC	homozygous	120131485
2	236051124	236051125	C	T	37	GENIC	homozygous	110318163
2	236051209	236051210	G	A	41	GENIC	homozygous	110318165
2	236051813	236051814	G	A	29	GENIC	possibly homozygous	111178703
2	236052056	236052057	T	C	19	GENIC	homozygous	111178705
2	236052382	236052383	A	G	33	GENIC	homozygous	110318167
2	236052512	236052513	T	C	38	GENIC	homozygous	110318169
2	236053272	236053273	T	C	31	GENIC	homozygous	110318171
2	236054216	236054217	A	G	22	GENIC	homozygous	110318175
2	236054893	236054894	A	C	41	GENIC	homozygous	110318177
2	236054901	236054902	A	G	39	GENIC	homozygous	110318179
2	236055449	236055450	G	A	42	GENIC	homozygous	110318181
2	236056342	236056343	T	C	26	GENIC	homozygous	111178707
2	236056905	236056906	A	G	24	GENIC	homozygous	110318190
2	236057140	236057141	A	G	28	GENIC	homozygous	110318192
2	236057778	236057779	T	A	30	GENIC	homozygous	110318196