chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	6655474	6655475	T	A	21	GENIC	possibly homozygous	47717940
16	6656880	6656881	A	G	24	GENIC	possibly homozygous	47256073
16	6656941	6656942	A	G	22	GENIC	homozygous	47717942
16	6657067	6657068	A	AAGGC	5	GENIC	homozygous	47879949
16	6657076	6657077	G	A	14	GENIC	homozygous	47717943
16	6657130	6657131	G	C	34	GENIC	possibly homozygous	47256074
16	6657191	6657192	A	G	20	GENIC	possibly homozygous	47256075
16	6657356	6657357	T	C	16	GENIC	possibly homozygous	47717945
16	6657848	6657849	T	C	20	GENIC	possibly homozygous	47717946
16	6658452	6658453	G	A	10	GENIC	possibly homozygous	47879951
16	6658934	6658935	T	A	21	GENIC	homozygous	47256080
16	6659223	6659224	T	C	32	GENIC	homozygous	47256081
16	6659506	6659507	T	C	29	GENIC	homozygous	47256082
16	6659710	6659711	C	CCT	10	GENIC	homozygous	47256084
16	6661344	6661345	T	C	18	GENIC	homozygous	47256088
16	6661386	6661387	C	T	9	GENIC	homozygous	47605382
16	6661388	6661389	T	C	6	GENIC	homozygous	47797371
16	6661633	6661634	T	C	16	GENIC	possibly homozygous	47256089
16	6663409	6663410	T	C	30	GENIC	possibly homozygous	47256092
16	6663438	6663439	T	C	23	GENIC	possibly homozygous	47717947
16	6664233	6664234	A	G	5	GENIC	homozygous	47256093
16	6664325	6664326	A	AAAAAAAAC	1	GENIC	homozygous	47919977
16	6665169	6665170	C	G	13	GENIC	homozygous	47901113
16	6672381	6672382	A	C	35	GENIC	possibly homozygous	47256109
16	6665178	6665182	CACG	----	13	GENIC	homozygous	47256097
16	6666028	6666029	A	G	8	GENIC	homozygous	47717950
16	6670538	6670539	T	C	28	GENIC	possibly homozygous	47256107
16	6675577	6675578	A	G	5	GENIC	homozygous	47717954
16	6675729	6675730	C	CT	1	GENIC	homozygous	47879953