chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10495924	10495925	C	T	26	GENIC	homozygous	110130769
19	10495996	10495997	G	C	16	GENIC	homozygous	125237190
19	10496905	10496906	G	C	16	GENIC	homozygous	109634050
19	10500386	10500387	G	T	37	GENIC	homozygous	109634056
19	10502418	10502419	G	A	8	GENIC	homozygous	125237191
19	10502470	10502471	G	C	14	GENIC	homozygous	125237192
19	10502599	10502600	T	A	9	GENIC	homozygous	125237194
19	10502643	10502644	T	A	24	GENIC	homozygous	125237195
19	10502780	10502781	C	T	9	GENIC	homozygous	110130772
19	10506446	10506447	T	G	15	GENIC	homozygous	125237196
19	10510421	10510422	C	G	12	GENIC	homozygous	125237198
19	10510438	10510439	C	A	15	GENIC	homozygous	125237199
19	10510460	10510461	C	A	10	GENIC	homozygous	125237200
19	10510489	10510490	C	A	14	GENIC	homozygous	125237201
19	10510500	10510501	C	A	16	GENIC	homozygous	125237202
19	10510621	10510622	G	T	4	GENIC	homozygous	125309935