chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	36155500	36155501	C	CCAGGACCT	1	GENIC	homozygous	49283033
14	36166152	36166153	G	A	14	GENIC	possibly homozygous	49512758
14	36172231	36172232	C	T	11	GENIC	possibly homozygous	48985055
14	36186019	36186020	A	C	10	GENIC	homozygous	48659901
14	36187134	36187135	A	G	23	GENIC	possibly homozygous	48985063
14	36187355	36187356	T	C	13	GENIC	possibly homozygous	48985065
14	36187601	36187602	G	A	32	GENIC	homozygous	48985067
14	36187729	36187730	G	A	18	GENIC	possibly homozygous	48985070
14	36188270	36188271	T	C	9	GENIC	homozygous	48985071
14	36188476	36188477	T	G	12	GENIC	possibly homozygous	48985073
14	36188573	36188574	T	C	13	GENIC	possibly homozygous	48659905
14	36188815	36188816	T	C	17	GENIC	homozygous	48659906
14	36188923	36188924	T	A	14	GENIC	heterozygous	48985075
14	36188924	36188925	T	A	12	GENIC	heterozygous	48985077
14	36193476	36193477	G	A	5	GENIC	homozygous	48659909
14	36196497	36196498	T	C	27	GENIC	homozygous	48659910
14	36196852	36196853	C	G	15	GENIC	heterozygous	48985079
14	36199753	36199754	C	T	21	GENIC	possibly homozygous	48985080
14	36201069	36201070	A	G	5	GENIC	heterozygous	48659913
14	36202282	36202283	C	T	15	GENIC	homozygous	48985085
14	36202341	36202342	C	T	9	GENIC	homozygous	48985087
14	36204934	36204935	C	T	17	GENIC	possibly homozygous	48659916
14	36206392	36206393	T	-	5	GENIC	heterozygous	48659917