chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	181700857	181700858	A	G	12	GENIC	heterozygous	60385470
3	181700862	181700863	C	T	12	GENIC	heterozygous	60385472
3	181700863	181700864	A	G	12	GENIC	heterozygous	60385474
3	181700870	181700871	A	G	12	GENIC	heterozygous	60385476
3	181700874	181700875	C	A	12	GENIC	heterozygous	60385478
3	181700877	181700878	G	A	13	GENIC	heterozygous	60385480
3	181701046	181701047	G	A	21	GENIC	heterozygous	60385482
3	181701092	181701093	G	A	25	GENIC	heterozygous	60385484
3	181701095	181701096	C	T	24	GENIC	heterozygous	60385486
3	181701096	181701097	A	G	23	GENIC	heterozygous	60385488
3	181701101	181701102	C	T	24	GENIC	heterozygous	60385490
3	181701102	181701103	A	G	23	GENIC	heterozygous	60385492
3	181701107	181701108	G	A	22	GENIC	heterozygous	60385494
3	181701125	181701126	G	A	19	GENIC	heterozygous	60385496
3	181701136	181701137	C	T	13	GENIC	heterozygous	60385498
3	181701137	181701138	C	A	13	GENIC	heterozygous	60385500
3	181701141	181701142	T	G	12	GENIC	heterozygous	60385502
3	181701477	181701478	G	A	15	GENIC	heterozygous	58447019
3	181701637	181701646	CTGCAGCTG	---------	16	GENIC	heterozygous	58447023
3	181702386	181702387	T	C	13	GENIC	heterozygous	58701574
3	181702621	181702622	G	A	26	GENIC	heterozygous	58447025
3	181704283	181704284	A	C	17	GENIC	heterozygous	58447029