chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4593428	4593429	C	T	29	GENIC	homozygous	109296160
20	4593996	4593997	A	G	24	GENIC	homozygous	109296162
20	4594669	4594670	A	G	23	GENIC	homozygous	109296164
20	4597096	4597097	C	T	37	GENIC	homozygous	109296166
20	4598193	4598194	A	G	49	GENIC	homozygous	109074823
20	4598342	4598343	G	A	36	GENIC	homozygous	109296168
20	4598560	4598561	T	C	36	GENIC	homozygous	109296170
20	4598957	4598958	C	T	39	GENIC	homozygous	109296172
20	4599094	4599095	C	T	31	GENIC	homozygous	109296174
20	4599343	4599344	C	T	13	GENIC	homozygous	109296176
20	4599828	4599829	T	C	15	GENIC	homozygous	109296178
20	4600965	4600966	C	T	39	GENIC	homozygous	109296180
20	4602889	4602890	G	A	28	GENIC	homozygous	109296182
20	4603508	4603509	C	A	35	GENIC	homozygous	109074843
20	4604395	4604396	T	C	22	GENIC	homozygous	109296184
20	4604400	4604401	A	G	20	GENIC	homozygous	109296186
20	4604678	4604679	G	A	24	GENIC	homozygous	109296188
20	4605414	4605415	C	T	21	GENIC	homozygous	109233550
20	4606258	4606259	G	A	39	GENIC	homozygous	109296190
20	4607420	4607421	C	T	20	GENIC	homozygous	109074864
20	4607834	4607835	T	G	13	GENIC	homozygous	109074868
20	4607959	4607960	T	C	21	GENIC	homozygous	109074870
20	4608156	4608157	T	C	21	GENIC	homozygous	109074872
20	4608751	4608752	C	T	24	GENIC	homozygous	109296192
20	4608756	4608757	G	A	24	GENIC	homozygous	109074882
20	4609543	4609544	C	T	17	GENIC	homozygous	109296194