chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	74484082	74484083	C	T	25	GENIC	homozygous	50961824
11	74484576	74484580	AAAC	----	20	GENIC	homozygous	50961825
11	74485126	74485127	A	G	31	GENIC	homozygous	50961826
11	74485254	74485288	ACACACACACACACACACACACACACACACACAC	----------------------------------	13	GENIC	heterozygous	51221199
11	74485907	74485908	T	C	34	GENIC	homozygous	50961828
11	74487671	74487672	G	GAA	6	GENIC	heterozygous	51189091
11	74488898	74488899	G	GCCTTTC	20	GENIC	homozygous	50961829
11	74489602	74489617	TAAAACAAAACAAAA	---------------	37	GENIC	homozygous	50961830
11	74489743	74489744	T	C	35	GENIC	homozygous	50961831
11	74490243	74490244	C	G	23	GENIC	homozygous	50961832
11	74490410	74490411	T	A	42	GENIC	homozygous	50961833
11	74490458	74490459	G	A	35	GENIC	homozygous	50961834
11	74491722	74491723	T	-	25	GENIC	homozygous	50961835
11	74492942	74492943	C	T	25	GENIC	homozygous	51221201
11	74493564	74493565	T	A	22	GENIC	homozygous	50961836
11	74493827	74493828	C	T	24	GENIC	homozygous	50961837
11	74494653	74494654	A	-	4	GENIC	homozygous	50832291
11	74494786	74494787	T	-	9	GENIC	homozygous	50961838
11	74495314	74495315	G	A	28	GENIC	homozygous	50961839
11	74496637	74496638	A	G	17	GENIC	homozygous	50961840
11	74496798	74496799	C	CTTT	5	GENIC	heterozygous	51189095
11	74497081	74497082	A	G	31	GENIC	homozygous	50961842
11	74497350	74497353	AAA	---	13	GENIC	homozygous	50961843
11	74497421	74497422	T	-	22	GENIC	homozygous	50892730
11	74498416	74498417	G	GAAAA	2	GENIC	homozygous	51221203
11	74498569	74498571	TG	--	15	GENIC	homozygous	50961844
11	74498943	74498944	C	CAA	20	GENIC	homozygous	50961845
11	74499034	74499035	T	A	18	GENIC	homozygous	50961846
11	74499883	74499884	C	CATATACTGAGACAAACTGATAAA	1	GENIC	homozygous	51221205
11	74500302	74500303	T	C	37	GENIC	homozygous	50961847
11	74501626	74501629	AAA	---	18	GENIC	possibly homozygous	50961849
11	74502318	74502319	T	C	2	GENIC	homozygous	50992492