chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	36982093	36982094	A	T	18	GENIC	homozygous	47651660
16	36982166	36982167	G	A	33	GENIC	homozygous	48090438
16	36982987	36982988	G	A	49	GENIC	homozygous	47651662
16	36983234	36983235	G	T	45	GENIC	homozygous	47651664
16	36985433	36985434	T	TG	25	GENIC	homozygous	48090439
16	36985434	36985435	T	G	26	GENIC	homozygous	48090440
16	36985656	36985657	T	G	19	GENIC	homozygous	47651673
16	36985660	36985661	G	C	22	GENIC	homozygous	47927909
16	36985695	36985696	C	T	29	GENIC	homozygous	48090441
16	36985707	36985708	T	G	32	GENIC	homozygous	47651675
16	36986153	36986154	G	A	51	GENIC	homozygous	48090442
16	36986287	36986288	G	A	40	GENIC	homozygous	48090443
16	36986513	36986514	G	A	35	GENIC	homozygous	48090444
16	36988735	36988736	T	TA	14	GENIC	homozygous	47382907
16	36989148	36989149	A	G	33	GENIC	homozygous	47651683
16	36990669	36990670	C	T	24	GENIC	homozygous	48090445
16	36991020	36991021	A	T	47	GENIC	homozygous	48090446
16	36991525	36991530	AAGTA	-----	33	GENIC	homozygous	48090447
16	36992667	36992668	T	C	20	GENIC	homozygous	48090448
16	36993640	36993646	TGTGTG	------	2	GENIC	heterozygous	47927911
16	36993642	36993646	TGTG	----	2	GENIC	heterozygous	47927912
16	36994078	36994079	A	G	14	GENIC	homozygous	48090449
16	36994457	36994458	T	C	28	GENIC	homozygous	47651696
16	36994729	36994730	A	-	15	GENIC	possibly homozygous	47651698
16	36995685	36995686	C	T	28	GENIC	homozygous	48090450
16	36997182	36997183	G	T	31	GENIC	homozygous	47651701
16	36997449	36997450	T	G	40	GENIC	homozygous	47651703
16	36998091	36998092	A	G	36	GENIC	homozygous	47651707
16	36999568	36999569	G	A	27	GENIC	homozygous	48090451
16	36999973	36999974	A	AT	9	GENIC	homozygous	48090452
16	37000228	37000229	A	G	35	GENIC	homozygous	47651718
16	37002546	37002547	C	G	27	GENIC	homozygous	47651720
16	37003151	37003152	T	C	14	GENIC	homozygous	47651723