chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	40782667	40782668	T	A	12	GENIC	homozygous	109267071
20	40782796	40782797	T	C	17	GENIC	heterozygous	119820926
20	40782800	40782801	T	C	16	GENIC	heterozygous	119820927
20	40784007	40784008	A	G	26	GENIC	homozygous	109315158
20	40784842	40784843	T	C	9	GENIC	homozygous	109267075
20	40785127	40785128	G	A	25	GENIC	homozygous	109315160
20	40785763	40785764	C	T	5	GENIC	homozygous	109315164
20	40785857	40785858	T	G	14	GENIC	homozygous	109315166
20	40785898	40785899	T	G	20	GENIC	homozygous	109315168
20	40786168	40786169	T	C	18	GENIC	homozygous	109465284
20	40786215	40786216	A	G	20	GENIC	homozygous	119820931
20	40786812	40786813	C	T	24	GENIC	homozygous	109401529
20	40788750	40788751	C	A	15	GENIC	heterozygous	119820932
20	40789132	40789133	A	T	48	GENIC	heterozygous	119820933
20	40790212	40790213	G	A	19	GENIC	homozygous	119820934
20	40790399	40790400	A	T	39	GENIC	possibly homozygous	119820935
20	40790466	40790467	C	T	48	GENIC	possibly homozygous	119820936
20	40790525	40790526	C	T	57	GENIC	heterozygous	119820937
20	40790550	40790551	A	G	53	GENIC	possibly homozygous	119820938
20	40790575	40790576	C	A	38	GENIC	homozygous	109315170
20	40793131	40793132	G	T	26	GENIC	homozygous	109315172
20	40793441	40793442	A	G	35	GENIC	homozygous	109267083
20	40793558	40793559	A	G	31	GENIC	possibly homozygous	109267085
20	40794670	40794671	G	T	26	GENIC	homozygous	109315174
20	40795494	40795495	A	T	6	GENIC	homozygous	109315176
20	40796073	40796074	G	C	16	GENIC	homozygous	109315178
20	40796323	40796324	A	G	19	GENIC	possibly homozygous	109267097
20	40796948	40796949	A	G	22	GENIC	homozygous	109267099
20	40797286	40797287	A	G	17	GENIC	homozygous	109267103
20	40797592	40797593	C	T	21	GENIC	homozygous	109315180
20	40798369	40798370	A	G	4	GENIC	homozygous	109267107
20	40800597	40800598	T	C	44	GENIC	homozygous	109267114
20	40800704	40800705	G	A	32	GENIC	homozygous	109267116
20	40800815	40800816	T	A	22	GENIC	homozygous	109267122