chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	263911939	263911939		G	16	GENIC	homozygous	127773735
2	263912199	263912200	C	G	4	GENIC	homozygous	120351894
2	263919590	263919590		G	18	GENIC	homozygous	127773739
2	263919610	263919610		T	18	GENIC	homozygous	127773740
2	263919635	263919635		T	16	GENIC	homozygous	127773741
2	263919653	263919654	T	C	16	GENIC	homozygous	110439654
2	263919628	263919629	G	T	18	GENIC	homozygous	110439652
2	263919642	263919643	A	T	15	GENIC	homozygous	120469921
2	263919643	263919644	T	A	15	GENIC	homozygous	120469922
2	263921333	263921333		TC	6	GENIC	homozygous	127773743
2	263921339	263921339		T	6	GENIC	homozygous	127773744
2	263921355	263921355		C	4	GENIC	homozygous	127773745
2	263921379	263921379		T	3	GENIC	homozygous	127773746
2	263921389	263921389		T	3	GENIC	homozygous	127773747
2	263921458	263921458		TC	4	GENIC	homozygous	130533285
2	263921398	263921398		T	3	GENIC	homozygous	130533282
2	263921445	263921446	G		5	GENIC	homozygous	130533283
2	263921455	263921456	A		4	GENIC	homozygous	130533284
2	263921476	263921476		C	1	GENIC	homozygous	130533286
2	263921491	263921492	C		1	GENIC	homozygous	130533287
2	263921465	263921466	C	G	3	GENIC	homozygous	110639537
2	263921478	263921479	C	T	1	GENIC	homozygous	110639539
2	263936295	263936296	A	G	41	GENIC	heterozygous	110439710
2	263936304	263936304		TGT	39	GENIC	heterozygous	127773751
2	263936329	263936330	G	A	43	GENIC	heterozygous	110439712
2	263936472	263936473	T	C	39	GENIC	heterozygous	110439714
2	263936473	263936474	G	A	39	GENIC	heterozygous	110439716
2	263936515	263936516	T		32	GENIC	heterozygous	127773752
2	263936543	263936544	C	T	35	GENIC	heterozygous	110439718
2	263936583	263936584	T	C	29	GENIC	heterozygous	110439720
2	263936601	263936602	C	T	22	GENIC	heterozygous	110439722
2	263936638	263936642	ACTC		18	GENIC	heterozygous	127773753
2	263936672	263936673	T	A	18	GENIC	heterozygous	110439724
2	263936704	263936705	G	A	16	GENIC	possibly homozygous	110439726