chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80928408	80928409	G	A	29	GENIC	homozygous	116106448
11	80928759	80928760	T	G	15	GENIC	homozygous	116106449
11	80928880	80928881	C	A	17	GENIC	homozygous	116106450
11	80929104	80929105	T	G	14	GENIC	homozygous	116106451
11	80930567	80930568	G	A	32	GENIC	homozygous	116066674
11	80930829	80930830	G	A	32	GENIC	homozygous	116106452
11	80930856	80930857	A	G	32	GENIC	homozygous	116106453
11	80931053	80931054	G	T	28	GENIC	homozygous	116066676
11	80932160	80932161	A	G	28	GENIC	homozygous	116106454
11	80933272	80933273	T	C	24	GENIC	homozygous	116106455
11	80935428	80935429	G	A	22	GENIC	homozygous	116106456
11	80941245	80941246	C	A	22	GENIC	homozygous	116106458
11	80941265	80941266	A	G	21	GENIC	homozygous	116106459
11	80943602	80943603	C	A	26	GENIC	homozygous	116106460
11	80944026	80944027	A	G	11	GENIC	homozygous	116106461
11	80944193	80944194	T	C	16	GENIC	homozygous	116110708
11	80958584	80958585	A	G	46	GENIC	homozygous	116106462
11	80962448	80962449	G	A	20	GENIC	homozygous	116106463
11	80962659	80962660	G	A	18	GENIC	homozygous	116106464
11	80962913	80962914	C	G	22	GENIC	homozygous	116106465
11	80964770	80964771	C	T	26	GENIC	homozygous	116106466
11	80970945	80970946	T	C	31	GENIC	homozygous	116106467
11	80973128	80973129	C	A	24	GENIC	homozygous	116106468
11	80973958	80973959	T	C	38	GENIC	homozygous	116106470
11	80975031	80975032	C	T	26	GENIC	homozygous	116106471
11	80976116	80976117	A	C	40	GENIC	homozygous	116106472
11	80980974	80980975	C	T	18	GENIC	homozygous	116106473
11	80981126	80981127	G	A	28	GENIC	homozygous	116106474