chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	64017510	64017510		A	18	GENIC	homozygous	138892431
11	64017761	64017762	A	T	23	GENIC	homozygous	139004221
11	64018239	64018240	C	T	21	GENIC	homozygous	139004222
11	64020906	64020907	C	T	20	GENIC	homozygous	139004225
11	64022903	64022904	A	C	29	GENIC	homozygous	139004226
11	64024215	64024216	C	T	20	GENIC	homozygous	139004227
11	64025546	64025547	A	T	22	GENIC	homozygous	139004229
11	64028145	64028146	A		20	GENIC	possibly homozygous	138892432
11	64028159	64028160	A	T	22	GENIC	homozygous	139004230
11	64029764	64029765	G	A	17	GENIC	homozygous	139004231
11	64031830	64031832	TA		21	GENIC	homozygous	138892433
11	64032778	64032779	A	G	17	GENIC	homozygous	139004232
11	64034673	64034674	A	G	30	GENIC	homozygous	139004233
11	64034758	64034759	G	A	21	GENIC	homozygous	139004234
11	64024658	64024658		CTGTTTCTC	28	GENIC	homozygous	146233123
11	64024744	64024745	T	C	28	GENIC	homozygous	146246658
11	64026243	64026244	C	T	15	GENIC	homozygous	146246659
11	64029235	64029236	G	A	17	GENIC	homozygous	146246660
11	64035272	64035273	T	C	20	GENIC	homozygous	146246661
11	64037231	64037232	C	T	26	GENIC	homozygous	139004235
11	64037409	64037410	A	G	17	GENIC	homozygous	139004236
11	64038247	64038248	A	G	15	GENIC	homozygous	139004237
11	64038460	64038461	T	A	12	GENIC	homozygous	139004238
11	64038549	64038550	T	C	16	GENIC	homozygous	139004239
11	64039513	64039514	T	C	25	GENIC	homozygous	139004240
11	64041200	64041201	T	C	20	GENIC	homozygous	139004241
11	64041369	64041370	G	A	16	GENIC	homozygous	139004242
11	64042550	64042550		C	29	GENIC	homozygous	138892434
11	64042550	64042551	A	T	29	GENIC	homozygous	139004245
11	64042624	64042625	G	T	25	GENIC	homozygous	139004246
11	64042800	64042801	G	A	20	GENIC	homozygous	139004247