chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	38114612	38114613	A		13	GENIC	homozygous	140388854
19	38115224	38115225	C	G	17	GENIC	homozygous	145079513
19	38117067	38117067		TT	22	GENIC	homozygous	140388855
19	38117803	38117803		AC	12	GENIC	homozygous	140388856
19	38118038	38118039	A	G	17	GENIC	homozygous	140453201
19	38117985	38117986	A	T	15	GENIC	homozygous	140453200
19	38116937	38116938	A	G	19	GENIC	homozygous	140453198
19	38117596	38117597	T	C	23	GENIC	homozygous	140453199
19	38118096	38118097	C	G	20	GENIC	homozygous	140453202
19	38120796	38120797	A	T	14	GENIC	homozygous	140453203
19	38121095	38121096	A	G	20	GENIC	homozygous	140453204
19	38121365	38121366	C	T	17	GENIC	homozygous	140453205
19	38118943	38118944	A		14	GENIC	heterozygous	403450749
19	38118943	38118944	A	G	14	GENIC	homozygous	155113361
19	38122731	38122732	C	A	12	GENIC	possibly homozygous	403450753
19	38122731	38122732	C		12	GENIC	heterozygous	403450754
19	38124055	38124056	A	G	9	GENIC	homozygous	140453206
19	38124560	38124561	A	C	25	GENIC	homozygous	140453207
19	38125355	38125355		C	23	GENIC	homozygous	140388859
19	38127720	38127721	C	G	17	GENIC	homozygous	140453208
19	38129095	38129096	G	A	14	GENIC	homozygous	145079514
19	38130912	38130912		AG	9	GENIC	homozygous	140388862
19	38131110	38131110		AC	16	GENIC	homozygous	140388863
19	38131280	38131281	T	C	19	GENIC	homozygous	140453210
19	38131425	38131426	G	A	16	GENIC	homozygous	145079516
19	38134709	38134710	C	G	11	GENIC	homozygous	145079517
19	38135733	38135734	A	G	10	GENIC	homozygous	142703634
19	38137685	38137686	G	T	20	GENIC	homozygous	140453221
19	38138813	38138814	T	C	17	GENIC	homozygous	155110687
19	38138813	38138814	T		17	GENIC	heterozygous	403450758
19	38141010	38141011	G	A	6	GENIC	homozygous	145079518