chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	35334788	35334789	C	T	25	GENIC	heterozygous	52302181
10	35336097	35336101	TATA	----	11	GENIC	heterozygous	51846437
10	35336212	35336213	C	A	14	GENIC	heterozygous	52137669
10	35352191	35352192	A	G	11	GENIC	homozygous	51407435
10	35352890	35352891	C	CAG	13	GENIC	heterozygous	51407439
10	35352969	35352970	A	AT	17	GENIC	homozygous	51407443
10	35359090	35359091	T	-	15	GENIC	homozygous	51407457
10	35359623	35359624	G	A	21	GENIC	heterozygous	51846446
10	35359792	35359793	T	-	13	GENIC	homozygous	51407459
10	35359879	35359880	A	G	22	GENIC	homozygous	51407461
10	35360054	35360055	A	G	20	GENIC	homozygous	51407463
10	35360400	35360401	T	C	20	GENIC	homozygous	51407465
10	35360504	35360505	T	A	19	GENIC	heterozygous	51846451
10	35361794	35361795	C	T	19	GENIC	homozygous	51407466
10	35363346	35363349	TTG	---	19	GENIC	heterozygous	51407474
10	35363499	35363500	C	T	11	GENIC	homozygous	51407478
10	35364504	35364505	G	A	20	GENIC	possibly homozygous	51846456
10	35365868	35365869	G	A	19	GENIC	heterozygous	51846459
10	35366057	35366058	C	A	15	GENIC	heterozygous	51846465
10	35366577	35366578	A	G	12	GENIC	homozygous	51407484
10	35368906	35368907	G	A	10	GENIC	heterozygous	52302185
10	35369313	35369314	G	A	17	GENIC	heterozygous	51407486
10	35369632	35369633	G	GTT	11	GENIC	homozygous	51407488
10	35369776	35369777	A	T	15	GENIC	homozygous	51846471
10	35371880	35371881	G	A	17	GENIC	heterozygous	51846479
10	35370262	35370263	G	A	16	GENIC	heterozygous	51846474
10	35370320	35370321	T	A	19	GENIC	heterozygous	51846476