chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	108236930	108236931	T	C	10	GENIC	homozygous	51953274
10	108237432	108237433	G	A	8	GENIC	homozygous	51953277
10	108237588	108237589	T	C	15	GENIC	possibly homozygous	51953280
10	108238118	108238119	G	A	17	GENIC	possibly homozygous	51953283
10	108238334	108238335	G	A	19	GENIC	possibly homozygous	51953286
10	108239007	108239008	C	T	25	GENIC	possibly homozygous	51953293
10	108240233	108240234	A	AG	1	GENIC	homozygous	51953299
10	108240371	108240372	T	A	18	GENIC	possibly homozygous	51953302
10	108240637	108240638	G	A	18	GENIC	possibly homozygous	51953305
10	108240787	108240788	G	A	16	GENIC	possibly homozygous	51953308
10	108240909	108240910	A	G	15	GENIC	possibly homozygous	51595337
10	108241442	108241443	G	A	5	GENIC	homozygous	51953311
10	108241598	108241599	T	C	10	GENIC	homozygous	51953314
10	108241604	108241605	T	C	10	GENIC	homozygous	51595339
10	108241712	108241713	C	T	24	GENIC	heterozygous	51953317
10	108242408	108242409	G	C	5	GENIC	homozygous	51953320
10	108245738	108245739	G	A	12	GENIC	possibly homozygous	51953323
10	108246353	108246354	G	A	12	GENIC	possibly homozygous	51953326
10	108246885	108246886	A	C	17	GENIC	possibly homozygous	51595343
10	108248787	108248788	G	A	15	GENIC	possibly homozygous	51953329
10	108249366	108249367	A	G	12	GENIC	possibly homozygous	51595347
10	108249539	108249540	C	A	17	GENIC	homozygous	51595350
10	108249637	108249638	A	G	1	GENIC	homozygous	51953332
10	108249857	108249858	G	A	10	GENIC	homozygous	51953341
10	108250758	108250762	AACA	----	5	GENIC	heterozygous	52331681
10	108250761	108250762	A	ATGTT	5	GENIC	heterozygous	52331683
10	108250781	108250782	G	A	4	GENIC	homozygous	51953355