chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	86972	86973	G	A	11	GENIC	homozygous	109622212
19	87031	87032	A	G	14	GENIC	homozygous	109622215
19	95464	95465	G	C	15	GENIC	homozygous	109757089
19	95683	95684	A	G	23	GENIC	homozygous	109622221
19	95693	95694	C	G	12	GENIC	homozygous	109622224
19	97061	97062	T	G	20	GENIC	homozygous	109757092
19	97133	97134	G	A	26	GENIC	homozygous	109757095
19	97663	97664	G	A	12	GENIC	homozygous	109757097
19	97821	97822	T	C	10	GENIC	homozygous	109757100
19	98010	98011	G	A	17	GENIC	homozygous	109757107
19	98083	98084	T	C	15	GENIC	homozygous	109757109
19	98162	98163	C	T	31	GENIC	homozygous	109757112
19	98438	98439	C	T	24	GENIC	heterozygous	109757115
19	98560	98561	G	A	21	GENIC	homozygous	109757117
19	98595	98596	T	A	20	GENIC	homozygous	109757120
19	98942	98943	T	C	15	GENIC	homozygous	109757124
19	98982	98983	G	A	8	GENIC	homozygous	109757127
19	98989	98990	C	T	12	GENIC	homozygous	109622230
19	99374	99375	T	C	9	GENIC	homozygous	109798814
19	99730	99731	C	T	22	GENIC	homozygous	109757130
19	99771	99772	G	A	11	GENIC	homozygous	109757133
19	99807	99808	G	C	17	GENIC	homozygous	109757135
19	100123	100124	T	C	9	GENIC	homozygous	109757140