chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47284030	47284031	T	G	33	GENIC	homozygous	116587371
10	47284272	47284273	A	G	24	GENIC	homozygous	116587373
10	47284410	47284411	C	T	31	GENIC	homozygous	116587375
10	47284524	47284525	G	A	30	GENIC	homozygous	116931751
10	47290326	47290327	A	G	21	GENIC	homozygous	116587377
10	47309205	47309206	A	T	25	GENIC	homozygous	116587379
10	47314291	47314292	T	A	12	GENIC	homozygous	116587381
10	47314803	47314804	G	A	15	GENIC	homozygous	116587383
10	47315004	47315005	G	A	18	GENIC	homozygous	116587385
10	47315128	47315129	C	T	21	GENIC	homozygous	116587387
10	47315208	47315209	T	C	18	GENIC	homozygous	116587389
10	47315706	47315707	C	T	11	GENIC	homozygous	116587391
10	47315734	47315735	C	T	20	GENIC	homozygous	116587393
10	47316054	47316055	C	T	29	GENIC	homozygous	116587395
10	47316057	47316058	G	T	29	GENIC	homozygous	116587397
10	47317015	47317016	A	C	35	GENIC	homozygous	116587399
10	47317360	47317361	G	A	34	GENIC	homozygous	116587401
10	47317364	47317365	C	T	33	GENIC	homozygous	116587403
10	47317405	47317406	T	C	30	GENIC	homozygous	116587405
10	47317561	47317562	T	C	24	GENIC	homozygous	116587407
10	47317990	47317991	T	A	38	GENIC	homozygous	116587409
10	47318776	47318777	C	T	29	GENIC	homozygous	116773387
10	47319190	47319191	G	A	24	GENIC	homozygous	116773389
10	47319895	47319896	T	G	16	GENIC	homozygous	116773391
10	47319920	47319921	T	C	23	GENIC	homozygous	116931753
10	47321163	47321164	C	T	33	GENIC	homozygous	116931755
10	47323570	47323571	A	G	29	GENIC	homozygous	116773395
10	47323833	47323834	A	G	28	GENIC	homozygous	116773397
10	47324828	47324829	G	A	28	GENIC	homozygous	116773401
10	47338987	47338988	T	C	24	GENIC	homozygous	116931757
10	47340879	47340880	A	G	23	GENIC	homozygous	116773409
10	47294546	47294547	T	C	1	GENIC	homozygous	116977648