chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	80967748	80967749	A		13	GENIC	homozygous	127643613
2	81013243	81013244	T		25	GENIC	homozygous	127643633
2	81013246	81013247	A		26	GENIC	homozygous	127643634
2	81013250	81013250		G	24	GENIC	homozygous	127643635
2	81013255	81013256	T	G	24	GENIC	homozygous	109876620
2	81013260	81013261	C		23	GENIC	homozygous	127643636
2	81013272	81013273	T		22	GENIC	homozygous	127643637
2	81013314	81013314		T	18	GENIC	homozygous	127643638
2	81013317	81013317		AGT	18	GENIC	homozygous	127643639
2	81013323	81013325	GC		19	GENIC	homozygous	127643640
2	81013328	81013329	C		19	GENIC	homozygous	127643641
2	81013339	81013339		G	21	GENIC	homozygous	127643642
2	81013358	81013359	G	A	24	GENIC	homozygous	109876622
2	81013378	81013382	GGGG		23	GENIC	homozygous	127643643
2	81013395	81013397	GT		18	GENIC	homozygous	127643644
2	81013402	81013402		G	19	GENIC	homozygous	127643645
2	81013407	81013407		G	20	GENIC	homozygous	127643646
2	81013433	81013433		T	21	GENIC	homozygous	127643647
2	81013445	81013446	C		23	GENIC	homozygous	127643648
2	81013450	81013451	C		22	GENIC	homozygous	127643649
2	81013454	81013455	T	A	21	GENIC	homozygous	120458963
2	81013458	81013459	G	T	21	GENIC	homozygous	120125234
2	81013467	81013467		G	22	GENIC	homozygous	127643650
2	81013489	81013489		T	19	GENIC	homozygous	127643651
2	81013506	81013507	G		17	GENIC	homozygous	127643652
2	81013509	81013509		A	17	GENIC	homozygous	127643653
2	81017001	81017002	C	T	29	GENIC	heterozygous	109876626
2	81018100	81018101	C	A	32	GENIC	heterozygous	109876630
2	81018217	81018218	G	A	14	GENIC	heterozygous	109876632
2	81018260	81018261	C	A	22	GENIC	heterozygous	109876634
2	81013383	81013384	G	T	22	GENIC	homozygous	120407331
2	81041387	81041388	T	A	20	GENIC	heterozygous	129876258
2	81036140	81036141	G	A	11	GENIC	heterozygous	130743505
2	81035266	81035267	C	A	12	GENIC	heterozygous	130262537