chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	24706422	24706423	C	A	32	GENIC	homozygous	109671394
19	24706558	24706559	G	A	26	GENIC	homozygous	109866094
19	24713122	24713123	T	G	19	GENIC	homozygous	109671396
19	24713640	24713641	A	G	21	GENIC	homozygous	109671398
19	24713841	24713842	A	G	42	GENIC	homozygous	109671400
19	24714265	24714266	A	G	25	GENIC	homozygous	109671402
19	24714499	24714500	C	T	36	GENIC	homozygous	109866096
19	24717047	24717048	A	G	27	GENIC	homozygous	109671404
19	24717260	24717261	G	A	38	GENIC	homozygous	109671406
19	24717341	24717342	T	C	38	GENIC	homozygous	109671408
19	24718987	24718988	C	T	35	GENIC	homozygous	109866098
19	24719230	24719231	T	A	34	GENIC	homozygous	109671412
19	24719376	24719377	C	G	25	GENIC	homozygous	109866100
19	24719860	24719861	A	G	23	GENIC	homozygous	109671414
19	24721322	24721323	A	G	25	GENIC	homozygous	109866102
19	24723067	24723068	G	A	18	GENIC	homozygous	109671416
19	24715989	24715990	A	C	25	GENIC	possibly homozygous	119602377
19	24719601	24719602	A	C	25	GENIC	possibly homozygous	119658033
19	24720872	24720873	G	A	29	GENIC	heterozygous	119678136
19	24725252	24725253	A	C	13	GENIC	possibly homozygous	119602379
19	24727050	24727051	A	G	28	GENIC	heterozygous	119678138
19	24728825	24728826	G	A	18	GENIC	homozygous	109866104