chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	13988775	13988776	T	C	37	GENIC	homozygous	109302764
20	13990082	13990083	C	G	26	GENIC	possibly homozygous	109463374
20	13992867	13992868	G	A	25	GENIC	possibly homozygous	109456427
20	13992903	13992904	C	A	19	GENIC	homozygous	119837044
20	13993116	13993117	C	T	22	GENIC	possibly homozygous	109331927
20	13993124	13993125	T	C	22	GENIC	homozygous	109542895
20	13993262	13993263	A	G	29	GENIC	homozygous	109100516
20	13993274	13993275	G	A	26	GENIC	homozygous	109528053
20	13993430	13993431	C	A	5	GENIC	homozygous	119815831
20	13994723	13994724	C	T	39	GENIC	homozygous	109100520
20	13994992	13994993	A	T	29	GENIC	homozygous	109302766
20	13995490	13995491	T	G	36	GENIC	possibly homozygous	109528055
20	13995697	13995698	C	A	35	GENIC	homozygous	109302768
20	13995260	13995261	C	T	16	GENIC	homozygous	119871674
20	13993375	13993376	A	C	40	GENIC	homozygous	109240676
20	13993389	13993390	C	A	31	GENIC	homozygous	109240677
20	13993417	13993418	T	G	35	GENIC	homozygous	119771160