chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	145361900	145361901	G	C	6	GENIC	homozygous	55767831
5	145363320	145363321	A	C	25	GENIC	possibly homozygous	55767841
5	145364001	145364002	C	T	21	GENIC	homozygous	55767844
5	145364976	145364977	A	G	14	GENIC	possibly homozygous	55767847
5	145365273	145365274	C	CAGTT	6	GENIC	heterozygous	55767850
5	145365891	145365892	C	T	13	GENIC	homozygous	55767855
5	145366834	145366835	G	A	21	GENIC	homozygous	55767858
5	145367301	145367302	T	G	12	GENIC	possibly homozygous	55767860
5	145368243	145368244	G	GA	2	GENIC	homozygous	55767863
5	145369071	145369072	A	G	13	GENIC	heterozygous	55767866
5	145369147	145369148	T	C	22	GENIC	homozygous	55767869
5	145373159	145373160	T	C	11	GENIC	homozygous	55767885
5	145373253	145373254	T	G	21	GENIC	possibly homozygous	55767887
5	145373669	145373670	C	T	20	GENIC	homozygous	55767890
5	145374274	145374275	C	G	13	GENIC	possibly homozygous	55767900
5	145376435	145376436	G	A	24	GENIC	possibly homozygous	55767909
5	145376586	145376587	G	A	35	GENIC	homozygous	55767912
5	145377734	145377735	T	G	21	GENIC	homozygous	55767915
5	145377759	145377760	A	G	23	GENIC	possibly homozygous	55767918
5	145377938	145377939	T	C	12	GENIC	homozygous	55767921
5	145378460	145378461	A	G	27	GENIC	homozygous	55767924
5	145378986	145378987	G	A	13	GENIC	heterozygous	55767927