chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	31630647	31630648	G	A	41	GENIC	homozygous	136066252
2	31631178	31631179	C	T	51	GENIC	homozygous	145354578
2	31632910	31632911	T	G	51	GENIC	possibly homozygous	145354579
2	31633917	31633918	T	C	21	GENIC	homozygous	145354580
2	31633964	31633965	A	G	22	GENIC	homozygous	136066255
2	31638505	31638506	A		40	GENIC	homozygous	145342417
2	31642711	31642718	GAGGTCA		39	GENIC	homozygous	145342418
2	31643141	31643142	A	G	33	GENIC	homozygous	136066266
2	31643431	31643432	G	A	46	GENIC	homozygous	136066267
2	31645102	31645103	A	T	26	GENIC	possibly homozygous	136066268
2	31651373	31651374	G	A	22	GENIC	homozygous	136066273
2	31652181	31652182	G		25	GENIC	homozygous	145342419
2	31652286	31652287	G	T	28	GENIC	homozygous	142930338
2	31652322	31652323	A	G	37	GENIC	homozygous	142930339
2	31652350	31652353	GGG		44	GENIC	homozygous	142893214
2	31652456	31652457	T	C	52	GENIC	homozygous	142930340
2	31651353	31651354	A	G	16	GENIC	heterozygous	403552177
2	31651348	31651349	A		17	GENIC	heterozygous	402996464
2	31651348	31651349	A	G	17	GENIC	heterozygous	402996465
2	31651353	31651354	A		16	GENIC	possibly homozygous	403552176
2	31651354	31651355	A		17	GENIC	heterozygous	403552178
2	31651354	31651355	A	G	17	GENIC	heterozygous	403552179