chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	75898984	75898985	A	G	18	GENIC	possibly homozygous	50964671
11	75900081	75900082	T	C	23	GENIC	possibly homozygous	50964674
11	75900244	75900245	G	A	24	GENIC	homozygous	51589311
11	75900635	75900636	A	AC	12	GENIC	possibly homozygous	50964675
11	75907163	75907164	T	TTG	1	GENIC	homozygous	51261373
11	75907182	75907183	G	GT	1	GENIC	homozygous	51241499
11	75907192	75907193	T	TTC	3	GENIC	heterozygous	51241500
11	75907488	75907489	C	-	15	GENIC	homozygous	50832666
11	75907891	75907892	G	GT	2	GENIC	heterozygous	51241501
11	75921011	75921012	G	A	9	GENIC	homozygous	51589313
11	75921357	75921358	C	CTTTT	1	GENIC	homozygous	51261374
11	75923108	75923109	A	G	3	GENIC	homozygous	51129045
11	75923149	75923150	A	T	9	GENIC	homozygous	51589315
11	75923158	75923159	T	C	9	GENIC	homozygous	51589317
11	75923210	75923211	A	C	4	GENIC	heterozygous	50964679
11	75923212	75923213	G	GAA	3	GENIC	heterozygous	50964680
11	75923213	75923214	A	-	3	GENIC	heterozygous	50832667