chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	205526828	205526828		TT	27	GENIC	homozygous	127729408
2	205527492	205527493	C	T	15	GENIC	homozygous	110214354
2	205528309	205528310	C	T	8	GENIC	homozygous	110214356
2	205529065	205529066	G	A	11	GENIC	homozygous	110214357
2	205529078	205529080	CA		11	GENIC	possibly homozygous	127729409
2	205529864	205529865	T	C	17	GENIC	homozygous	110214358
2	205531787	205531788	G	A	19	GENIC	homozygous	110214359
2	205532348	205532349	T	G	20	GENIC	homozygous	110214360
2	205532591	205532591		T	27	GENIC	homozygous	127729410
2	205533114	205533115	C	G	10	GENIC	homozygous	110214361
2	205538433	205538434	A	G	12	GENIC	homozygous	110214362
2	205544752	205544753	A	G	15	GENIC	homozygous	110214363
2	205545812	205545813	T	G	15	GENIC	homozygous	110214364
2	205545975	205545976	T	A	18	GENIC	homozygous	110214365
2	205547131	205547132	A	G	17	GENIC	homozygous	110214366
2	205547862	205547863	T	A	22	GENIC	homozygous	110214367
2	205549042	205549043	G	A	16	GENIC	homozygous	110214368
2	205552122	205552124	TA		11	GENIC	homozygous	127729411
2	205541969	205541972	AAC		10	GENIC	heterozygous	129869906