chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	102415815	102415816	T	TG	5	GENIC	heterozygous	61486354
1	102416861	102416862	A	G	2	GENIC	heterozygous	61486356
1	102419142	102419143	C	T	12	GENIC	possibly homozygous	61486357
1	102419861	102419862	G	-	10	GENIC	homozygous	61486359
1	102422802	102422803	A	G	14	GENIC	homozygous	61486360
1	102425036	102425037	A	T	14	GENIC	homozygous	61486361
1	102425089	102425090	A	-	9	INTERGENIC	possibly homozygous	61486362
1	102425596	102425597	C	T	20	INTERGENIC	homozygous	61486363
1	102426741	102426742	A	G	17	INTERGENIC	homozygous	61486364
1	102427011	102427012	G	A	22	INTERGENIC	homozygous	61486365
1	102428096	102428097	G	T	16	INTERGENIC	homozygous	61486366
1	102428904	102428905	T	C	7	INTERGENIC	homozygous	61486367
1	102428981	102428982	G	GT	12	INTERGENIC	heterozygous	61486368
1	102429419	102429420	C	A	17	INTERGENIC	homozygous	61486369
1	102429697	102429698	T	C	12	INTERGENIC	possibly homozygous	61486370
1	102429867	102429868	A	G	10	INTERGENIC	possibly homozygous	61486371
1	102432361	102432362	C	-	12	GENIC	homozygous	61486374
1	102432412	102432413	A	T	24	GENIC	homozygous	61486375
1	102432725	102432726	A	G	7	GENIC	homozygous	61486376
1	102432945	102432950	CTGGT	-----	2	GENIC	homozygous	61486377
1	102433881	102433883	TC	--	4	GENIC	homozygous	61486379
1	102434325	102434326	T	C	13	GENIC	homozygous	61486383
1	102434388	102434389	A	T	10	GENIC	homozygous	61486384
1	102434422	102434423	C	T	13	GENIC	homozygous	61486385
1	102435232	102435233	G	C	24	GENIC	possibly homozygous	61486386
1	102435968	102435969	T	-	5	GENIC	heterozygous	61486387
1	102436012	102436013	G	-	10	GENIC	heterozygous	61486388
1	102436233	102436234	T	C	8	GENIC	homozygous	61486389
1	102437076	102437077	T	TTCAG	6	GENIC	homozygous	61486390
1	102454532	102454533	A	-	2	GENIC	homozygous	61486392
1	102455010	102455011	T	-	1	GENIC	homozygous	62229293
1	102456507	102456508	C	T	9	GENIC	heterozygous	61486393
1	102456668	102456669	A	G	11	GENIC	homozygous	61486394