chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	50968715	50968716	G	A	28	GENIC	possibly homozygous	139941301
16	50970381	50970382	A	G	19	GENIC	homozygous	139941302
16	50971321	50971322	A	C	24	GENIC	homozygous	139941303
16	50971609	50971610	C	T	16	GENIC	homozygous	139941304
16	50973789	50973790	T		10	GENIC	heterozygous	403398605
16	50973789	50973790	T	C	10	GENIC	homozygous	403398606
16	50973791	50973792	T		10	GENIC	heterozygous	403398607
16	50973791	50973792	T	C	10	GENIC	homozygous	403398608
16	50975086	50975087	T	C	20	GENIC	homozygous	139941305
16	50976036	50976036		TGTA	9	GENIC	homozygous	139837168
16	50976118	50976118		TG	9	GENIC	homozygous	139837169
16	50976200	50976200		TGTGTGTGTGTGTATGTCTGTGTGTATG	10	GENIC	homozygous	139837170
16	50976988	50976988		TA	18	GENIC	homozygous	139837171
16	50976993	50976994	C	A	19	GENIC	homozygous	139941308
16	50978945	50978946	A	G	27	GENIC	homozygous	139941309
16	50979645	50979646	T	G	16	GENIC	heterozygous	139941310
16	50981522	50981523	T	A	24	GENIC	homozygous	139941312
16	50983067	50983068	T	C	23	GENIC	homozygous	139941313
16	50983376	50983377	A	G	20	GENIC	homozygous	139941314
16	50986046	50986047	A	G	21	GENIC	homozygous	139941315
16	50990827	50990828	A		18	GENIC	homozygous	139837172
16	50991482	50991483	T	C	26	GENIC	homozygous	139941317
16	50992869	50992870	A	C	19	GENIC	homozygous	139941318
16	50994215	50994216	T	G	24	GENIC	homozygous	139941319
16	50994285	50994286	C	T	22	GENIC	homozygous	139941320
16	50994289	50994290	A	G	20	GENIC	homozygous	139941321
16	50995822	50995823	G	A	14	GENIC	homozygous	139941322
16	50996236	50996237	T	C	17	GENIC	homozygous	139941323
16	50996616	50996616		G	10	GENIC	homozygous	139837174
16	50997490	50997491	C	T	26	GENIC	homozygous	139941325
16	50997526	50997527	C	T	22	GENIC	homozygous	139941326