chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4593428	4593429	C	T	5	GENIC	homozygous	109296160
20	4593996	4593997	A	G	13	GENIC	homozygous	109296162
20	4594669	4594670	A	G	10	GENIC	homozygous	109296164
20	4597096	4597097	C	T	15	GENIC	homozygous	109296166
20	4598342	4598343	G	A	15	GENIC	homozygous	109296168
20	4598428	4598429	C	A	16	GENIC	homozygous	109074827
20	4598560	4598561	T	C	20	GENIC	homozygous	109296170
20	4598957	4598958	C	T	14	GENIC	homozygous	109296172
20	4599094	4599095	C	T	14	GENIC	homozygous	109296174
20	4599343	4599344	C	T	16	GENIC	homozygous	109296176
20	4599828	4599829	T	C	19	GENIC	homozygous	109296178
20	4600965	4600966	C	T	9	GENIC	homozygous	109296180
20	4602889	4602890	G	A	22	GENIC	homozygous	109296182
20	4603508	4603509	C	A	22	GENIC	homozygous	109074843
20	4604395	4604396	T	C	35	GENIC	homozygous	109296184
20	4604400	4604401	A	G	32	GENIC	homozygous	109296186
20	4604678	4604679	G	A	25	GENIC	homozygous	109296188
20	4605414	4605415	C	T	25	GENIC	homozygous	109233550
20	4606258	4606259	G	A	39	GENIC	homozygous	109296190
20	4607420	4607421	C	T	16	GENIC	homozygous	109074864
20	4607834	4607835	T	G	10	GENIC	homozygous	109074868
20	4607959	4607960	T	C	15	GENIC	homozygous	109074870
20	4608594	4608595	A	C	11	GENIC	homozygous	109074876
20	4608606	4608607	G	T	14	GENIC	homozygous	109074878
20	4608635	4608636	T	C	14	GENIC	homozygous	109074880
20	4608751	4608752	C	T	21	GENIC	homozygous	109296192
20	4608756	4608757	G	A	18	GENIC	homozygous	109074882
20	4609543	4609544	C	T	12	GENIC	homozygous	109296194
20	4609561	4609562	A	C	22	GENIC	heterozygous	109296196