chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	142753587	142753589	CA		23	GENIC	heterozygous	130250730
2	142755953	142755954	G	C	63	GENIC	homozygous	110760430
2	142825916	142825917	A	G	32	GENIC	homozygous	110760621
2	142833042	142833043	C	A	4	GENIC	homozygous	110038353
2	142784252	142784253	A		18	GENIC	homozygous	127685967
2	142784253	142784254	T	G	18	GENIC	homozygous	120127319
2	142784256	142784257	C	G	19	GENIC	homozygous	110594858
2	142784262	142784263	T	G	17	GENIC	homozygous	110594860
2	142784263	142784264	T	G	17	GENIC	homozygous	110594862
2	142792072	142792073	G	C	13	GENIC	heterozygous	134925607
2	142795210	142795211	C	T	52	GENIC	homozygous	120206254
2	142807788	142807789	C	T	52	GENIC	homozygous	120206255
2	142842177	142842180	CGC		19	GENIC	homozygous	127685969
2	142842597	142842598	C		20	GENIC	homozygous	127685970
2	142858132	142858134	TG		17	GENIC	possibly homozygous	131291358
2	142860848	142860848		C	37	GENIC	homozygous	127685971
2	142879534	142879535	G	T	43	GENIC	homozygous	120206256
2	142883303	142883304	C		55	GENIC	homozygous	127685972
2	142883368	142883369	C		49	GENIC	homozygous	127685973
2	142883371	142883372	C	T	49	GENIC	homozygous	120127321
2	142883373	142883374	C		51	GENIC	homozygous	127685974
2	142883539	142883540	C	T	47	GENIC	homozygous	110760818
2	142885309	142885310	A	C	39	GENIC	homozygous	120206257
2	142883836	142883837	C	G	48	GENIC	homozygous	120372652