chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	637171	637172	A	C	51	GENIC	homozygous	109798874
19	637743	637744	T	G	39	GENIC	homozygous	109757414
19	638032	638033	C	T	38	GENIC	possibly homozygous	109757417
19	638533	638534	C	T	44	GENIC	homozygous	109757419
19	638904	638904		GG	40	GENIC	homozygous	132232644
19	638964	638965	T	C	43	GENIC	homozygous	109798877
19	639812	639813	T	C	42	GENIC	homozygous	109757422
19	640011	640012	G	A	41	GENIC	possibly homozygous	109757424
19	640013	640014	G	T	41	GENIC	possibly homozygous	109757427
19	640708	640709	C	A	50	GENIC	homozygous	109757430
19	640965	640966	G	C	46	GENIC	homozygous	109757432
19	641393	641394	T	C	38	GENIC	homozygous	109757437
19	641507	641507		T	37	GENIC	possibly homozygous	132232645
19	641813	641814	C	T	32	GENIC	homozygous	109757439
19	642390	642391	C	T	51	GENIC	homozygous	109757441
19	643228	643229	G	A	48	GENIC	homozygous	109757444
19	643802	643804	TA		31	GENIC	homozygous	132232646
19	645030	645031	A	G	41	GENIC	homozygous	109757446
19	645142	645143	G	C	37	GENIC	homozygous	109757449
19	645390	645391	G		46	GENIC	homozygous	132232647
19	645530	645531	C	G	57	GENIC	homozygous	109622613
19	645900	645901	A	C	40	GENIC	homozygous	109833100
19	645901	645902	G	T	40	GENIC	homozygous	109833102
19	645918	645918		TT	37	GENIC	homozygous	129578358
19	645920	645922	GA		35	GENIC	homozygous	129578359
19	645922	645923	A	T	34	GENIC	homozygous	109833105
19	645925	645926	A	T	33	GENIC	homozygous	109833108