chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	76956283	76956284	C	T	2	GENIC	homozygous	110563560
2	76956303	76956304	C	T	4	GENIC	homozygous	109853533
2	76956321	76956322	G	A	9	GENIC	heterozygous	109853535
2	76956359	76956360	A	G	22	GENIC	homozygous	109853537
2	76956518	76956519	C	T	17	GENIC	homozygous	109853539
2	76956563	76956564	A	C	5	GENIC	homozygous	110563561
2	76956572	76956573	G	A	4	GENIC	homozygous	110563562
2	76957188	76957189	G	A	25	GENIC	homozygous	109853541
2	76958211	76958212	C	T	13	GENIC	heterozygous	109853543
2	76958243	76958244	A	G	23	GENIC	possibly homozygous	109853545
2	76958246	76958247	C	T	23	GENIC	possibly homozygous	109853547
2	76958252	76958253	T	A	27	GENIC	possibly homozygous	109853549
2	76958261	76958262	T	C	35	GENIC	heterozygous	110563565
2	76958284	76958285	A	G	44	GENIC	heterozygous	109853551
2	76958286	76958287	A	C	47	GENIC	heterozygous	110563566
2	76958322	76958323	A	G	35	GENIC	heterozygous	109853555
2	76958324	76958325	C	T	33	GENIC	homozygous	109853557
2	76958330	76958331	T	C	32	GENIC	heterozygous	109853559
2	76959954	76959955	T	A	9	GENIC	homozygous	110563567
2	76959972	76959973	C	T	15	GENIC	homozygous	110563568
2	76959973	76959974	C	T	15	GENIC	homozygous	110563569
2	76960016	76960017	T	C	21	GENIC	homozygous	110563570
2	76960076	76960077	A	T	5	GENIC	homozygous	110563571
2	76961439	76961440	A	T	10	GENIC	homozygous	110563573
2	76961470	76961471	T	C	20	GENIC	possibly homozygous	110563574
2	76961494	76961495	A	C	25	GENIC	possibly homozygous	110563575
2	76961501	76961502	T	G	24	GENIC	possibly homozygous	110563576
2	76961504	76961505	A	T	23	GENIC	possibly homozygous	110563577
2	76961513	76961514	A	T	23	GENIC	possibly homozygous	110563578
2	76959941	76959942	C	T	5	GENIC	homozygous	110940456