chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	74484082	74484083	C	T	15	GENIC	homozygous	50961824
11	74484576	74484580	AAAC	----	7	GENIC	homozygous	50961825
11	74485126	74485127	A	G	28	GENIC	homozygous	50961826
11	74485254	74485288	ACACACACACACACACACACACACACACACACAC	----------------------------------	8	GENIC	heterozygous	51221199
11	74485907	74485908	T	C	27	GENIC	homozygous	50961828
11	74488898	74488899	G	GCCTTTC	19	GENIC	homozygous	50961829
11	74489602	74489617	TAAAACAAAACAAAA	---------------	24	GENIC	homozygous	50961830
11	74490000	74490001	C	T	20	GENIC	homozygous	51588091
11	74490243	74490244	C	G	17	GENIC	homozygous	50961832
11	74490410	74490411	T	A	20	GENIC	homozygous	50961833
11	74490458	74490459	G	A	15	GENIC	homozygous	50961834
11	74491722	74491723	T	-	22	GENIC	homozygous	50961835
11	74493547	74493548	G	-	17	GENIC	homozygous	51588093
11	74493564	74493565	T	A	21	GENIC	homozygous	50961836
11	74493827	74493828	C	T	28	GENIC	homozygous	50961837
11	74494653	74494654	A	-	10	GENIC	possibly homozygous	50832291
11	74494786	74494787	T	-	13	GENIC	heterozygous	50961838
11	74495314	74495315	G	A	16	GENIC	homozygous	50961839
11	74496637	74496638	A	G	29	GENIC	homozygous	50961840
11	74496794	74496795	T	-	20	GENIC	homozygous	51588095
11	74496795	74496796	A	C	16	GENIC	homozygous	51588097
11	74496798	74496799	C	CT	14	GENIC	homozygous	51588098
11	74497081	74497082	A	G	13	GENIC	possibly homozygous	50961842
11	74497350	74497353	AAA	---	13	GENIC	homozygous	50961843
11	74497421	74497422	T	-	9	GENIC	homozygous	50892730
11	74498416	74498417	G	GAAAA	2	GENIC	heterozygous	51221203
11	74498569	74498571	TG	--	13	GENIC	homozygous	50961844
11	74498943	74498944	C	CAA	17	GENIC	homozygous	50961845
11	74499034	74499035	T	A	16	GENIC	homozygous	50961846
11	74500302	74500303	T	C	23	GENIC	homozygous	50961847
11	74501626	74501629	AAA	---	9	GENIC	homozygous	50961849
11	74502318	74502319	T	C	6	GENIC	homozygous	50992492