chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	74480321	74480322	A	G	45	GENIC	homozygous	51125246
11	74482989	74482990	G	C	12	GENIC	homozygous	50961823
11	74483148	74483149	G	A	43	GENIC	homozygous	51125249
11	74483307	74483328	TCTGAGAGTATACAGTTTCTT	---------------------	18	GENIC	homozygous	51125252
11	74484572	74484580	AAACAAAC	--------	12	GENIC	homozygous	51125255
11	74484906	74484907	T	C	52	GENIC	homozygous	51125257
11	74485281	74485282	C	T	31	GENIC	heterozygous	51125260
11	74486222	74486223	T	C	32	GENIC	homozygous	51125263
11	74488898	74488899	G	GCCTTTC	21	GENIC	homozygous	50961829
11	74489602	74489617	TAAAACAAAACAAAA	---------------	25	GENIC	heterozygous	50961830
11	74491722	74491723	T	-	36	GENIC	homozygous	50961835
11	74492982	74492983	C	-	33	GENIC	homozygous	51125266
11	74493564	74493565	T	A	32	GENIC	homozygous	50961836
11	74494653	74494654	A	-	15	GENIC	heterozygous	50832291
11	74487675	74487676	G	GAA	10	GENIC	heterozygous	50832288
11	74487675	74487676	G	GA	10	GENIC	heterozygous	50832289
11	74494652	74494653	G	GA	15	GENIC	heterozygous	50832290
11	74494786	74494787	T	-	28	GENIC	homozygous	50961838
11	74495201	74495202	G	A	66	GENIC	homozygous	51125269
11	74496097	74496098	T	G	26	GENIC	heterozygous	51125273
11	74496798	74496799	C	CTT	2	GENIC	homozygous	50961841
11	74496938	74496939	T	-	20	GENIC	homozygous	51125276
11	74497081	74497082	A	G	32	GENIC	homozygous	50961842
11	74497284	74497285	C	A	42	GENIC	homozygous	51125280
11	74497424	74497425	T	G	41	GENIC	possibly homozygous	51125283
11	74498569	74498571	TG	--	43	GENIC	homozygous	50961844
11	74498943	74498944	C	CAA	35	GENIC	homozygous	50961845
11	74500196	74500197	T	C	53	GENIC	homozygous	51125286
11	74500302	74500303	T	C	49	GENIC	homozygous	50961847
11	74501272	74501273	T	-	3	GENIC	homozygous	51019829
11	74501628	74501629	A	-	13	GENIC	heterozygous	51074513
11	74502318	74502319	T	C	6	GENIC	homozygous	50992492
11	74502482	74502483	G	A	26	GENIC	homozygous	51125289