chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54184643	54184644	C	T	32	GENIC	homozygous	109733113
19	54184708	54184709	A	G	32	GENIC	homozygous	109733115
19	54184736	54184737	C	T	25	GENIC	homozygous	109733117
19	54184737	54184738	C	G	25	GENIC	homozygous	109733119
19	54185092	54185093	A	C	21	GENIC	homozygous	109733121
19	54185103	54185104	C	T	20	GENIC	homozygous	109733123
19	54185287	54185288	A	G	23	GENIC	homozygous	109733125
19	54185327	54185328	G	T	17	GENIC	homozygous	109733127
19	54185466	54185467	C	G	32	GENIC	homozygous	109733129
19	54185540	54185541	T	C	24	GENIC	homozygous	109733131
19	54185860	54185861	C	A	32	GENIC	homozygous	109733133
19	54186101	54186102	T	C	31	GENIC	homozygous	109733137
19	54186176	54186177	C	T	27	GENIC	homozygous	109733139
19	54186760	54186761	C	T	17	GENIC	homozygous	109733141
19	54187152	54187153	G	A	27	GENIC	homozygous	109733143
19	54187167	54187168	A	G	25	GENIC	homozygous	109733145
19	54187913	54187914	A	G	18	GENIC	possibly homozygous	109825531
19	54188669	54188670	A	G	14	GENIC	homozygous	109733147
19	54191131	54191132	A	G	37	GENIC	homozygous	109733149
19	54191232	54191233	T	C	20	GENIC	homozygous	109875847
19	54191234	54191235	A	G	20	GENIC	homozygous	109875849
19	54192358	54192359	A	G	35	GENIC	homozygous	109733153
19	54193312	54193313	T	G	8	GENIC	homozygous	109733155
19	54193363	54193364	C	T	10	GENIC	homozygous	109733157
19	54193605	54193606	C	A	25	GENIC	homozygous	109733159
19	54199672	54199673	C	G	11	GENIC	homozygous	109733161
19	54200152	54200153	G	A	20	GENIC	homozygous	109733163
19	54204102	54204103	C	T	35	GENIC	homozygous	109733169
19	54204998	54204999	G	A	28	GENIC	possibly homozygous	109733171
19	54205439	54205440	C	T	28	GENIC	homozygous	109733173
19	54205872	54205873	C	G	37	GENIC	heterozygous	109733175