chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	50395534	50395535	A	G	7	GENIC	homozygous	109280297
20	50396122	50396123	A	G	26	GENIC	homozygous	109219806
20	50396343	50396344	G	A	27	GENIC	homozygous	109219808
20	50398324	50398325	C	G	4	GENIC	homozygous	109384394
20	50399751	50399752	C	T	17	GENIC	homozygous	109219812
20	50400207	50400208	A	T	7	GENIC	homozygous	109219814
20	50400208	50400209	G	A	7	GENIC	homozygous	109219816
20	50400262	50400263	A	G	14	GENIC	homozygous	109219818
20	50400469	50400470	T	C	14	GENIC	homozygous	109219820
20	50401166	50401167	A	G	6	GENIC	homozygous	109219824
20	50401360	50401361	A	G	18	GENIC	homozygous	109219827
20	50401430	50401431	T	A	15	GENIC	homozygous	109280316
20	50401495	50401496	C	T	19	GENIC	homozygous	109219829
20	50401730	50401731	A	G	5	GENIC	homozygous	109349997
20	50401758	50401759	T	G	3	GENIC	heterozygous	125214896
20	50403193	50403194	C	T	5	GENIC	heterozygous	109219833
20	50403299	50403300	A	G	21	GENIC	homozygous	109219835
20	50404258	50404259	A	T	8	GENIC	homozygous	119849923
20	50404328	50404329	G	A	17	GENIC	homozygous	109219839
20	50404742	50404743	T	C	9	GENIC	homozygous	109280318
20	50406389	50406390	T	C	24	GENIC	homozygous	109219841
20	50406926	50406927	G	A	16	GENIC	homozygous	109219843
20	50407007	50407008	T	C	17	GENIC	homozygous	109219845
20	50407382	50407383	T	C	20	GENIC	homozygous	109219847
20	50403772	50403773	C	T	13	GENIC	homozygous	109319775
20	50405130	50405131	G	C	14	GENIC	homozygous	109319777
20	50405163	50405164	G	T	16	GENIC	homozygous	109319779
20	50406275	50406276	A	C	20	GENIC	homozygous	109319781
20	50407526	50407527	G	A	12	GENIC	homozygous	109319783
20	50403933	50403934	G	T	6	GENIC	homozygous	125195518
20	50409523	50409524	G	A	12	GENIC	homozygous	125195519
20	50404011	50404012	G	C	4	GENIC	homozygous	125207589