chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	31934539	31934540	A	G	13	GENIC	homozygous	53863108
7	31935789	31935790	A	C	21	GENIC	homozygous	53863110
7	31937974	31937975	G	C	21	GENIC	possibly homozygous	53863117
7	31938575	31938576	T	C	14	GENIC	possibly homozygous	53863119
7	31940290	31940291	G	T	22	GENIC	homozygous	53863120
7	31940562	31940563	G	T	11	GENIC	homozygous	53863121
7	31940598	31940599	C	CA	13	GENIC	possibly homozygous	53863122
7	31941435	31941436	A	T	14	GENIC	possibly homozygous	53863123
7	31941761	31941762	C	T	13	GENIC	heterozygous	54350151
7	31942438	31942439	G	A	23	GENIC	possibly homozygous	53863124
7	31942809	31942810	A	-	5	GENIC	homozygous	53863125
7	31944773	31944774	C	CT	2	GENIC	homozygous	53863129
7	31944871	31944872	T	C	9	GENIC	heterozygous	53863130
7	31945238	31945239	C	A	4	GENIC	homozygous	53863131
7	31945374	31945381	AAAAAAA	-------	1	GENIC	homozygous	54189341
7	31946270	31946271	G	C	14	GENIC	homozygous	53863133
7	31947459	31947460	G	A	26	GENIC	homozygous	53863134
7	31948868	31948869	A	G	21	GENIC	possibly homozygous	53863135
7	31949041	31949042	C	T	16	GENIC	homozygous	53863136
7	31949555	31949556	A	G	12	GENIC	possibly homozygous	53863137
7	31951301	31951302	C	CTGTGTAGGCCACATGACAG	1	GENIC	homozygous	53863139
7	31951538	31951539	G	A	11	GENIC	possibly homozygous	53863140
7	31952498	31952499	A	-	3	GENIC	heterozygous	54966204
7	31953750	31953751	T	C	21	GENIC	possibly homozygous	53863145
7	31955156	31955157	A	G	23	GENIC	homozygous	53863146
7	31955659	31955660	T	C	16	GENIC	homozygous	53863147
7	31957170	31957171	A	G	18	GENIC	possibly homozygous	53863148
7	31958003	31958004	A	G	16	GENIC	homozygous	53863150
7	31958067	31958068	A	C	6	GENIC	homozygous	53863151
7	31958560	31958561	G	C	4	GENIC	homozygous	53863153