chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	46995320	46995321	C	T	12	GENIC	homozygous	141721289
5	46995426	46995427	G	A	14	GENIC	homozygous	141721290
5	46995800	46995801	A	G	9	GENIC	homozygous	141721291
5	46995929	46995930	A	G	9	GENIC	homozygous	141721292
5	47000291	47000292	C	T	14	GENIC	homozygous	141721297
5	46996136	46996137	T	A	20	GENIC	homozygous	141721293
5	46996801	46996802	G	A	17	GENIC	homozygous	141721294
5	46999135	46999136	T	C	13	GENIC	homozygous	141721295
5	46999234	46999235	C	T	21	GENIC	homozygous	137455650
5	46999952	46999953	C	T	16	GENIC	homozygous	141721296
5	47000171	47000172	G	A	13	GENIC	homozygous	137455651
5	46997448	46997454	GGGAGA		7	GENIC	homozygous	141681191
5	46997499	46997500	A		7	GENIC	homozygous	143178722
5	47000628	47000629	G	A	14	GENIC	homozygous	137455653
5	47000645	47000645		GA	16	GENIC	homozygous	141681192
5	47000698	47000699	G		17	GENIC	homozygous	137306070
5	47000700	47000705	GAAAG		17	GENIC	homozygous	137306071
5	47001945	47001946	G	A	21	GENIC	homozygous	137455656
5	47002324	47002325	T	C	14	GENIC	homozygous	137455657
5	46997499	46997500	A	G	7	GENIC	heterozygous	403139927