chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	160047267	160047268	G	A	26	GENIC	homozygous	111791250
3	160048492	160048493	C	T	26	GENIC	homozygous	111791252
3	160048963	160048964	C	T	26	GENIC	homozygous	111791254
3	160049796	160049797	A	G	15	GENIC	homozygous	111791256
3	160051075	160051076	G	A	23	GENIC	homozygous	111791262
3	160051567	160051568	G	A	28	GENIC	homozygous	111791264
3	160052679	160052680	G	A	16	GENIC	homozygous	111791272
3	160053197	160053198	C	T	14	GENIC	homozygous	111791274
3	160054414	160054415	A	G	18	GENIC	homozygous	111791276
3	160054589	160054590	G	T	21	GENIC	homozygous	111791278
3	160057677	160057678	C	T	25	GENIC	homozygous	111791288
3	160061624	160061625	C	T	12	GENIC	homozygous	111791290
3	160062662	160062663	A	T	20	GENIC	homozygous	111791292
3	160062808	160062809	C	T	22	GENIC	homozygous	111791294
3	160065811	160065812	C	T	11	GENIC	homozygous	111791302
3	160065843	160065844	G	T	13	GENIC	homozygous	111791304
3	160068317	160068318	T	C	8	GENIC	homozygous	111791306
3	160072361	160072362	T	C	12	GENIC	homozygous	111791308
3	160073657	160073658	A	G	19	GENIC	homozygous	111791312
3	160074187	160074188	G	A	28	GENIC	homozygous	111791314
3	160074486	160074487	A	G	15	GENIC	homozygous	111791318
3	160081130	160081131	A	G	19	GENIC	homozygous	111791326
3	160083048	160083049	C	T	26	GENIC	homozygous	111791328
3	160083342	160083343	T	C	20	GENIC	homozygous	111791330
3	160089597	160089598	A	T	40	GENIC	homozygous	111791332
3	160096896	160096897	G	A	16	GENIC	homozygous	111791334
3	160100036	160100037	C	G	23	GENIC	homozygous	111791336
3	160100380	160100381	T	C	14	GENIC	homozygous	111791340
3	160100417	160100418	T	G	18	GENIC	homozygous	119652558
3	160100418	160100419	G	T	18	GENIC	homozygous	111791342
3	160100442	160100443	A	G	18	GENIC	homozygous	111791344