chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	145361900	145361901	G	C	12	GENIC	homozygous	55767831
5	145363113	145363114	A	-	3	GENIC	homozygous	57040518
5	145363698	145363699	G	GAC	12	GENIC	homozygous	55916901
5	145364001	145364002	C	T	27	GENIC	possibly homozygous	55767844
5	145364976	145364977	A	G	19	GENIC	possibly homozygous	55767847
5	145365273	145365274	C	CAGTT	7	GENIC	homozygous	55767850
5	145365364	145365365	T	C	25	GENIC	homozygous	55916907
5	145365509	145365510	C	T	17	GENIC	homozygous	55916909
5	145367107	145367108	C	T	19	GENIC	homozygous	55916913
5	145367301	145367302	T	G	18	GENIC	possibly homozygous	55767860
5	145367841	145367842	A	C	19	GENIC	homozygous	56291408
5	145367882	145367883	T	G	6	GENIC	homozygous	56291409
5	145367888	145367889	C	T	6	GENIC	homozygous	56291410
5	145369147	145369148	T	C	23	GENIC	possibly homozygous	55767869
5	145370313	145370314	A	-	1	GENIC	homozygous	56458957
5	145370535	145370536	G	A	20	GENIC	possibly homozygous	56291411
5	145370676	145370677	A	AAAAC	5	GENIC	homozygous	56291412
5	145371166	145371167	G	T	5	GENIC	homozygous	57040520
5	145371167	145371168	T	C	4	GENIC	homozygous	57040522
5	145373159	145373160	T	C	14	GENIC	possibly homozygous	55767885
5	145373253	145373254	T	G	11	GENIC	homozygous	55767887
5	145378991	145378992	T	TC	2	GENIC	homozygous	55916921
5	145373669	145373670	C	T	20	GENIC	homozygous	55767890