chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	76324180	76324180		A	21	GENIC	homozygous	147482707
2	76324364	76324365	C	T	31	GENIC	homozygous	147492572
2	76325048	76325049	A	C	22	GENIC	homozygous	136159806
2	76327168	76327169	A	C	14	GENIC	homozygous	136159807
2	76327181	76327182	A	C	19	GENIC	homozygous	136159808
2	76327190	76327191	C	A	21	GENIC	homozygous	136159809
2	76328096	76328097	A	T	23	GENIC	homozygous	136159810
2	76328513	76328514	A	C	13	GENIC	homozygous	136159812
2	76328746	76328747	A	G	26	GENIC	homozygous	136159813
2	76330121	76330122	G	C	38	GENIC	homozygous	136159814
2	76330704	76330705	C	T	22	GENIC	homozygous	136159815
2	76330994	76330995	T	C	31	GENIC	homozygous	136159816
2	76331135	76331136	T	C	32	GENIC	homozygous	136159817
2	76331189	76331190	T		20	GENIC	homozygous	135918389
2	76327165	76327165		CC	12	GENIC	homozygous	135918385
2	76327188	76327188		GC	20	GENIC	homozygous	135918386
2	76327617	76327617		T	25	GENIC	homozygous	135918387
2	76329159	76329160	C		36	GENIC	homozygous	135918388
2	76332427	76332431	TTGT		33	GENIC	homozygous	147482708
2	76332495	76332496	C	T	29	GENIC	homozygous	136159819
2	76333068	76333069	C	T	26	GENIC	homozygous	147492573