chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	37461213	37461214	T	C	13	GENIC	homozygous	117989344
10	37464034	37464035	C	T	8	GENIC	homozygous	117989345
10	37466729	37466730	G	C	22	GENIC	homozygous	117989346
10	37467010	37467011	T	G	13	GENIC	heterozygous	118065624
10	37467702	37467703	T	C	21	GENIC	homozygous	117989349
10	37469219	37469220	C	T	28	GENIC	heterozygous	118065625
10	37471238	37471239	A	G	23	GENIC	homozygous	117989350
10	37472707	37472708	A	G	28	GENIC	heterozygous	117989351
10	37474855	37474856	G	A	16	GENIC	homozygous	117989352
10	37477565	37477566	C	T	20	GENIC	homozygous	117989353
10	37480280	37480281	A	G	21	GENIC	homozygous	117989354
10	37480463	37480464	A	G	30	GENIC	homozygous	117989355
10	37481071	37481072	T	C	18	GENIC	homozygous	117989356
10	37481399	37481400	C	T	31	GENIC	homozygous	117989357
10	37481422	37481423	T	G	23	GENIC	homozygous	117989358
10	37483277	37483278	T	G	30	GENIC	homozygous	117989359
10	37473422	37473423	G	A	29	GENIC	heterozygous	118035204
10	37485990	37485991	G	T	16	GENIC	homozygous	117989360
10	37487002	37487003	A	G	36	GENIC	homozygous	117989361
10	37488446	37488447	T	C	23	GENIC	homozygous	117989362
10	37489028	37489029	T	C	33	GENIC	heterozygous	117989363
10	37490281	37490282	C	A	15	GENIC	homozygous	117989364
10	37491065	37491066	A	G	7	GENIC	homozygous	117989365
10	37492613	37492614	T	G	16	GENIC	homozygous	117989367
10	37496237	37496238	G	A	20	GENIC	homozygous	117989368
10	37497642	37497643	A	G	33	GENIC	homozygous	117989369
10	37501562	37501563	G	A	28	GENIC	homozygous	117989370
10	37503179	37503180	C	T	21	GENIC	homozygous	117989371
10	37505681	37505682	C	T	27	GENIC	heterozygous	117989372
10	37489036	37489037	T	C	30	GENIC	heterozygous	118074447