chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	76324464	76324465	T	G	14	GENIC	homozygous	136159802
2	76324589	76324590	G	A	13	GENIC	homozygous	136159803
2	76324742	76324743	C	T	20	GENIC	homozygous	136159804
2	76324892	76324893	T	C	10	GENIC	homozygous	136159805
2	76325048	76325049	A	C	21	GENIC	homozygous	136159806
2	76327165	76327165		CC	3	GENIC	homozygous	135918385
2	76327168	76327169	A	C	3	GENIC	homozygous	136159807
2	76327181	76327182	A	C	16	GENIC	homozygous	136159808
2	76327188	76327188		GC	3	GENIC	homozygous	135918386
2	76327190	76327191	C	A	17	GENIC	homozygous	136159809
2	76327617	76327617		T	23	GENIC	homozygous	135918387
2	76328096	76328097	A	T	17	GENIC	homozygous	136159810
2	76328284	76328285	C	T	13	GENIC	homozygous	136159811
2	76328513	76328514	A	C	12	GENIC	homozygous	136159812
2	76328746	76328747	A	G	12	GENIC	homozygous	136159813
2	76329159	76329160	C		23	GENIC	homozygous	135918388
2	76330121	76330122	G	C	18	GENIC	homozygous	136159814
2	76330704	76330705	C	T	17	GENIC	homozygous	136159815
2	76330994	76330995	T	C	21	GENIC	homozygous	136159816
2	76331135	76331136	T	C	25	GENIC	homozygous	136159817
2	76331189	76331190	T		23	GENIC	homozygous	135918389
2	76331615	76331616	T	C	9	GENIC	homozygous	136159818
2	76332495	76332496	C	T	27	GENIC	homozygous	136159819