chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	51022066	51022067	G	GAA	2	GENIC	heterozygous	49052523
15	51022067	51022068	G	GGA	2	GENIC	heterozygous	49052525
15	51023132	51023133	T	C	26	GENIC	homozygous	48306371
15	51023964	51023965	T	C	10	GENIC	homozygous	48306372
15	51023967	51023968	T	C	11	GENIC	homozygous	48306373
15	51024584	51024585	G	A	18	GENIC	homozygous	48306374
15	51024788	51024789	G	A	17	GENIC	possibly homozygous	48306375
15	51024862	51024863	T	C	18	GENIC	heterozygous	48306376
15	51024922	51024923	C	T	13	GENIC	homozygous	48306377
15	51024930	51024931	G	T	17	GENIC	homozygous	48306378
15	51025161	51025162	T	C	23	GENIC	possibly homozygous	48306379
15	51025398	51025399	T	TTTGC	7	GENIC	homozygous	48306380
15	51025615	51025616	C	T	30	GENIC	possibly homozygous	48306381
15	51025641	51025642	A	G	24	GENIC	homozygous	48306382
15	51025942	51025943	C	G	13	GENIC	homozygous	48306383
15	51025952	51025953	G	A	9	GENIC	homozygous	48306384
15	51026084	51026085	G	T	17	GENIC	possibly homozygous	48306385
15	51026302	51026303	G	GCTGGAGATAC	2	GENIC	homozygous	48306386
15	51026373	51026374	G	C	20	GENIC	homozygous	48306387
15	51026444	51026445	C	T	20	GENIC	homozygous	48306388
15	51028409	51028410	G	A	21	GENIC	possibly homozygous	48306389
15	51028662	51028663	A	G	23	GENIC	possibly homozygous	48306390
15	51029570	51029571	T	C	16	GENIC	homozygous	48306391
15	51029641	51029642	T	C	12	GENIC	homozygous	48306392
15	51029711	51029712	C	T	4	GENIC	homozygous	48306393
15	51030773	51030774	C	T	18	GENIC	homozygous	48306394
15	51030790	51030791	T	C	21	GENIC	homozygous	48306395
15	51031633	51031634	A	T	18	GENIC	possibly homozygous	48306396
15	51032063	51032064	T	G	12	GENIC	homozygous	48306397