chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	31250849	31250850	T	C	23	GENIC	homozygous	45518241
20	31251790	31251791	C	CAA	7	GENIC	heterozygous	45846677
20	31253298	31253299	A	G	29	GENIC	homozygous	45518251
20	31253378	31253379	A	AC	26	GENIC	homozygous	45518253
20	31253763	31253764	A	G	18	GENIC	homozygous	45518255
20	31254683	31254684	C	T	22	GENIC	possibly homozygous	45785904
20	31255931	31255932	G	C	27	GENIC	homozygous	45785905
20	31256472	31256473	T	C	35	GENIC	homozygous	45518261
20	31256724	31256725	C	T	28	GENIC	homozygous	45518263
20	31256986	31256987	G	A	27	GENIC	homozygous	45518265
20	31257617	31257618	C	T	21	GENIC	homozygous	45518267
20	31257731	31257747	GTGTGTGTGTGTATGT	----------------	24	GENIC	homozygous	45518269
20	31258721	31258722	C	T	28	GENIC	homozygous	45518271
20	31258727	31258728	G	A	29	GENIC	homozygous	45785906
20	31259008	31259009	C	T	37	GENIC	homozygous	45785907
20	31259591	31259592	G	C	32	GENIC	homozygous	45518273
20	31260458	31260459	G	A	32	GENIC	homozygous	45518275
20	31260973	31260974	G	A	22	GENIC	homozygous	45518277
20	31261020	31261021	C	G	17	GENIC	homozygous	45785908
20	31261778	31261779	G	GGGATTAGT	15	GENIC	homozygous	45785909
20	31262757	31262759	TT	--	8	GENIC	homozygous	45785910
20	31263680	31263681	G	A	32	GENIC	homozygous	45785913
20	31264837	31264838	A	G	30	GENIC	homozygous	45518289
20	31264874	31264875	A	AC	26	GENIC	homozygous	45785914
20	31265973	31265974	C	T	22	GENIC	homozygous	45785915
20	31266036	31266037	C	T	18	GENIC	homozygous	45785916
20	31266578	31266579	T	-	12	GENIC	possibly homozygous	45518293
20	31266612	31266613	G	A	21	GENIC	homozygous	45518295
20	31266655	31266656	G	GT	5	GENIC	heterozygous	45846678