chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	44683362	44683363	A	G	27	GENIC	homozygous	109211524
20	44683615	44683616	T	C	21	GENIC	homozygous	109211526
20	44684476	44684477	C	T	31	GENIC	homozygous	109211528
20	44684605	44684606	A	G	22	GENIC	homozygous	109273697
20	44685276	44685277	T	C	16	GENIC	homozygous	109211530
20	44685420	44685421	T	C	17	GENIC	homozygous	109211532
20	44686255	44686256	G	T	31	GENIC	homozygous	109211534
20	44688456	44688457	G	C	7	GENIC	homozygous	109211538
20	44689971	44689972	T	G	19	GENIC	homozygous	109211540
20	44690675	44690676	T	C	4	GENIC	homozygous	109211544
20	44691294	44691295	C	G	30	GENIC	homozygous	109211546
20	44692512	44692513	A	G	19	GENIC	homozygous	109211548
20	44693537	44693538	A	C	9	GENIC	homozygous	109211550
20	44693710	44693711	G	T	12	GENIC	homozygous	109273705
20	44694209	44694210	T	C	19	GENIC	homozygous	109211552
20	44694218	44694219	C	A	17	GENIC	homozygous	109211554
20	44694219	44694220	C	G	17	GENIC	homozygous	109211556
20	44694223	44694224	C	G	16	GENIC	homozygous	109211558
20	44694225	44694226	C	A	16	GENIC	homozygous	109211560
20	44701449	44701450	G	A	21	GENIC	homozygous	109211562
20	44705983	44705984	T	C	13	GENIC	homozygous	109273726
20	44709060	44709061	C	G	15	GENIC	homozygous	109211564
20	44709142	44709143	G	C	33	GENIC	homozygous	109211566
20	44709786	44709787	T	C	26	GENIC	homozygous	109211568
20	44716648	44716649	G	A	24	GENIC	homozygous	109211570
20	44716994	44716995	G	A	24	GENIC	homozygous	109211572
20	44719871	44719872	G	A	17	GENIC	homozygous	109211574
20	44721000	44721001	A	G	23	GENIC	homozygous	109211580
20	44720011	44720012	C	A	16	GENIC	homozygous	109273732
20	44720219	44720220	T	A	10	GENIC	homozygous	109211576
20	44720496	44720497	T	C	16	GENIC	homozygous	109211578
20	44721453	44721454	C	T	16	GENIC	homozygous	109211582
20	44721460	44721461	G	A	17	GENIC	homozygous	109211584
20	44721779	44721780	G	A	13	GENIC	homozygous	109211586