chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	211220178	211220179	C	T	48	GENIC	homozygous	110224232
2	211224349	211224350	T	A	19	GENIC	heterozygous	110224235
2	211225105	211225106	T	C	61	GENIC	homozygous	110224236
2	211225158	211225159	G	A	55	GENIC	possibly homozygous	110224237
2	211225175	211225176	A	G	52	GENIC	homozygous	110224238
2	211225233	211225234	A	G	46	GENIC	homozygous	110224239
2	211226616	211226617	A	G	46	GENIC	homozygous	110224242
2	211227321	211227322	G	A	53	GENIC	homozygous	111011855
2	211227383	211227384	T	G	71	GENIC	homozygous	110224244
2	211227394	211227395	A	T	66	GENIC	possibly homozygous	110224245
2	211227788	211227789	C	T	70	GENIC	homozygous	111011857
2	211227885	211227886	T	C	47	GENIC	homozygous	110224246
2	211227926	211227927	A	T	41	GENIC	homozygous	110224247
2	211227994	211227995	T	G	36	GENIC	homozygous	110224248
2	211229664	211229665	A	G	56	GENIC	homozygous	110224249
2	211229841	211229842	A	T	68	GENIC	homozygous	110224250
2	211229996	211229997	T	G	49	GENIC	homozygous	110224252
2	211230128	211230129	G	C	47	GENIC	homozygous	111011859
2	211230808	211230809	C	T	50	GENIC	homozygous	110224254
2	211230892	211230893	T	A	50	GENIC	homozygous	110224255
2	211231505	211231506	T	C	46	GENIC	homozygous	110224256
2	211232962	211232963	T	C	37	GENIC	homozygous	110224257
2	211235442	211235443	C	T	28	GENIC	homozygous	110909380