chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	55596601	55596602	G	C	19	GENIC	homozygous	116978013
10	55596650	55596651	G	C	17	GENIC	homozygous	116782674
10	55597525	55597526	T	C	18	GENIC	homozygous	116602635
10	55597801	55597802	C	T	14	GENIC	homozygous	116602637
10	55597916	55597917	C	T	14	GENIC	homozygous	116602639
10	55600088	55600089	C	T	15	GENIC	homozygous	117994771
10	55600402	55600403	T		20	GENIC	homozygous	128818972
10	55600171	55600173	TC		11	GENIC	homozygous	128818971
10	55599538	55599539	C	T	13	GENIC	homozygous	116934875
10	55601376	55601376		GATT	24	GENIC	homozygous	128818973
10	55601694	55601695	C	T	13	GENIC	homozygous	116602641
10	55601905	55601906	A	G	18	GENIC	homozygous	116602643
10	55601916	55601917	C	T	19	GENIC	homozygous	116602645
10	55602276	55602276		TGGGTTTCTC	12	GENIC	homozygous	128818974
10	55602494	55602495	G	A	12	GENIC	homozygous	117410897
10	55602580	55602581	T	C	20	GENIC	homozygous	116602647
10	55602606	55602607	C	A	19	GENIC	homozygous	117994772
10	55603052	55603053	T	C	11	GENIC	homozygous	116782678
10	55604511	55604512	T	A	21	GENIC	homozygous	116602649
10	55608202	55608202		C	23	GENIC	homozygous	128818975
10	55608941	55608942	C	T	15	GENIC	homozygous	116602653
10	55609709	55609710	G	A	21	GENIC	homozygous	116602655
10	55612654	55612655	C	T	18	GENIC	homozygous	116602659
10	55613216	55613217	T	C	16	GENIC	possibly homozygous	116602663
10	55613243	55613243		AACTGTCT	13	GENIC	possibly homozygous	128818976
10	55615266	55615267	G	A	25	GENIC	homozygous	116602667