chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	39089883	39089884	A	G	32	GENIC	homozygous	109816118
19	39090089	39090090	T	C	25	GENIC	homozygous	109816120
19	39090206	39090207	C	G	25	GENIC	homozygous	109816122
19	39090277	39090278	T	C	20	GENIC	homozygous	109816124
19	39090928	39090929	G	A	30	GENIC	homozygous	109816126
19	39091238	39091239	G	A	29	GENIC	homozygous	109816128
19	39091356	39091357	A	G	31	GENIC	homozygous	109816130
19	39091892	39091893	C	G	26	GENIC	homozygous	109816132
19	39092240	39092241	C	T	15	GENIC	homozygous	109816134
19	39092247	39092248	T	C	17	GENIC	homozygous	109816136
19	39092834	39092835	A	G	12	GENIC	homozygous	109816140
19	39092907	39092908	T	C	24	GENIC	homozygous	109816142
19	39092958	39092959	T	G	16	GENIC	homozygous	109816144
19	39093001	39093002	A	T	22	GENIC	homozygous	109816146
19	39093401	39093402	G	A	25	GENIC	homozygous	109816148
19	39094160	39094161	A	G	20	GENIC	homozygous	109816150
19	39099127	39099128	A	T	19	GENIC	homozygous	109869933
19	39101979	39101980	T	C	14	GENIC	homozygous	109816153
19	39102244	39102245	T	C	36	GENIC	homozygous	109816155
19	39102246	39102247	C	T	37	GENIC	homozygous	109816157
19	39102247	39102248	A	T	37	GENIC	homozygous	109816159
19	39103829	39103830	A	T	23	GENIC	homozygous	109816161
19	39104768	39104769	A	G	25	GENIC	homozygous	109816163
19	39105049	39105050	G	A	27	GENIC	homozygous	109816165
19	39106038	39106039	T	G	30	GENIC	homozygous	109816167
19	39106175	39106176	A	G	28	GENIC	homozygous	109816169
19	39106871	39106872	G	T	18	GENIC	homozygous	109816171
19	39107228	39107229	G	A	19	GENIC	homozygous	109816173
19	39108544	39108545	A	G	21	GENIC	homozygous	109816175
19	39109244	39109245	C	T	25	GENIC	homozygous	109816177
19	39109499	39109500	T	C	18	GENIC	homozygous	109816179
19	39110747	39110748	C	T	29	GENIC	homozygous	109816181
19	39111883	39111884	A	G	23	GENIC	homozygous	109816183
19	39112786	39112787	A	G	18	GENIC	homozygous	109816187
19	39115107	39115108	A	G	17	GENIC	homozygous	109816189