chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	40619297	40619298	A		16	GENIC	homozygous	129688530
20	40651291	40651333	CATTCACTGGGGGTTCAGTCTTGGCAGGACCAAGGGCTTCCC		23	GENIC	homozygous	129688531
20	40659044	40659044		ATTATC	51	GENIC	homozygous	129688532
20	40669186	40669193	CGGATGT		16	GENIC	homozygous	129688533
20	40669195	40669200	AGACG		16	GENIC	homozygous	129688534
20	40669203	40669208	GCGTC		15	GENIC	homozygous	129688535
20	40669216	40669217	C		13	GENIC	homozygous	129688536
20	40669220	40669221	G		12	GENIC	homozygous	129688537
20	40669228	40669229	A		11	GENIC	homozygous	129688538
20	40687816	40687817	G	T	41	GENIC	homozygous	109266543
20	40690213	40690214	C		43	GENIC	homozygous	129688539
20	40694175	40694176	G	A	11	GENIC	homozygous	124671573
20	40703622	40703624	AC		31	GENIC	heterozygous	129688540
20	40687904	40687905	C	T	45	GENIC	homozygous	109195986
20	40669611	40669612	C	A	10	GENIC	possibly homozygous	109401514
20	40686557	40686558	T	G	51	GENIC	heterozygous	129712636
20	40686560	40686561	C	T	51	GENIC	heterozygous	129712637