chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47283641	47283642	G	A	16	GENIC	homozygous	116587369
10	47284030	47284031	T	G	29	GENIC	homozygous	116587371
10	47284272	47284273	A	G	23	GENIC	homozygous	116587373
10	47284410	47284411	C	T	17	GENIC	homozygous	116587375
10	47290326	47290327	A	G	14	GENIC	homozygous	116587377
10	47309205	47309206	A	T	14	GENIC	homozygous	116587379
10	47313692	47313693	A	C	19	GENIC	homozygous	126382171
10	47313896	47313897	T	G	15	GENIC	homozygous	117993633
10	47314803	47314804	G	A	12	GENIC	homozygous	116587383
10	47315004	47315005	G	A	17	GENIC	homozygous	116587385
10	47315128	47315129	C	T	14	GENIC	homozygous	116587387
10	47315706	47315707	C	T	21	GENIC	homozygous	116587391
10	47315734	47315735	C	T	26	GENIC	homozygous	116587393
10	47316054	47316055	C	T	4	GENIC	homozygous	116587395
10	47317015	47317016	A	C	7	GENIC	homozygous	116587399
10	47317360	47317361	G	A	18	GENIC	homozygous	116587401
10	47317364	47317365	C	T	15	GENIC	homozygous	116587403
10	47317405	47317406	T	C	9	GENIC	homozygous	116587405
10	47317561	47317562	T	C	9	GENIC	homozygous	116587407
10	47317990	47317991	T	A	12	GENIC	homozygous	116587409