chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	157676912	157676913	A	G	17	GENIC	homozygous	108326220
1	157680180	157680181	G	A	16	GENIC	homozygous	108326232
1	157682328	157682329	G	A	22	GENIC	homozygous	108326236
1	157685343	157685344	G	T	8	GENIC	homozygous	108326248
1	157687730	157687731	C	T	34	GENIC	homozygous	108326256
1	157688031	157688032	T	C	11	GENIC	homozygous	109154457
1	157686788	157686789	A	C	16	GENIC	homozygous	109154455
1	157688655	157688656	A	T	13	GENIC	homozygous	109154459
1	157689678	157689679	C	T	13	GENIC	homozygous	108326266
1	157689681	157689682	T	C	15	GENIC	homozygous	108326268
1	157691380	157691381	T	C	17	GENIC	homozygous	108326280
1	157693797	157693798	A	G	23	GENIC	homozygous	108326290
1	157694450	157694451	A	G	13	GENIC	homozygous	108326296
1	157694795	157694796	A	C	22	GENIC	homozygous	108326300
1	157694848	157694849	C	T	20	GENIC	homozygous	108326302
1	157695737	157695738	G	A	9	GENIC	homozygous	108326304
1	157696116	157696117	T	G	5	GENIC	homozygous	108326306
1	157696144	157696145	T	C	18	GENIC	homozygous	108326310
1	157696363	157696364	A	T	25	GENIC	homozygous	108326312
1	157696440	157696441	T	C	19	GENIC	homozygous	108326314
1	157696907	157696908	C	A	27	GENIC	homozygous	108326316
1	157697277	157697278	C	T	24	GENIC	homozygous	108326318
1	157697494	157697495	T	C	20	GENIC	homozygous	108326320
1	157699704	157699705	C	T	16	GENIC	homozygous	120506807
1	157699841	157699842	G	A	17	GENIC	homozygous	108326323