chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9708248	9708249	T	C	54	GENIC	homozygous	130050488
20	9708352	9708353	G	A	52	GENIC	possibly homozygous	130050489
20	9708779	9708780	G	T	65	GENIC	possibly homozygous	130050490
20	9709525	9709526	T	C	69	GENIC	homozygous	130050491
20	9712640	9712641	G	A	58	GENIC	homozygous	130050492
20	9712669	9712670	A	G	56	GENIC	homozygous	130050493
20	9714562	9714563	A	G	22	GENIC	homozygous	130050496
20	9709947	9709947		TTG	65	GENIC	homozygous	129982263
20	9713811	9713812	T		42	GENIC	homozygous	129982264
20	9713870	9713871	C	A	42	GENIC	possibly homozygous	130050494
20	9714107	9714108	A	G	46	GENIC	homozygous	130050495
20	9715013	9715013		GAGC	42	GENIC	homozygous	129982265
20	9715416	9715417	T	C	66	GENIC	homozygous	130050497
20	9717095	9717095		A	51	GENIC	homozygous	129982266
20	9719411	9719412	G	C	47	GENIC	homozygous	130050498
20	9720357	9720358	A	T	15	GENIC	homozygous	130050499
20	9721392	9721393	G	A	63	GENIC	homozygous	130050500
20	9721755	9721756	C	A	63	GENIC	possibly homozygous	130050501
20	9723040	9723041	C	T	46	GENIC	homozygous	130050502
20	9723047	9723048	A	G	46	GENIC	homozygous	130050503
20	9723251	9723255	ATCT		50	GENIC	homozygous	129982267
20	9723458	9723459	G	C	12	GENIC	homozygous	130050504
20	9723462	9723463	G	C	11	GENIC	homozygous	130050505
20	9723470	9723471	C		2	GENIC	homozygous	129982268
20	9723687	9723688	C	G	32	GENIC	homozygous	130050506
20	9723701	9723716	ATCTATCTATCTATC		37	GENIC	homozygous	129982269
20	9723816	9723817	G	A	50	GENIC	homozygous	130050507
20	9723876	9723877	A	G	49	GENIC	homozygous	130050508
20	9725318	9725319	T	C	52	GENIC	homozygous	130050509
20	9730814	9730815	C		40	GENIC	possibly homozygous	403913932
20	9730814	9730815	C	G	40	GENIC	heterozygous	155134294