chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	23936573	23936574	T	G	9	GENIC	homozygous	109888126
19	23936586	23936587	A	G	9	GENIC	homozygous	109802409
19	23936736	23936737	G	A	21	GENIC	homozygous	109669531
19	23936878	23936879	A	G	18	GENIC	homozygous	109669533
19	23937241	23937242	G	T	15	GENIC	homozygous	109669535
19	23938002	23938003	T	C	36	GENIC	homozygous	109669539
19	23938171	23938172	T	C	25	GENIC	homozygous	109669541
19	23938255	23938256	G	A	30	GENIC	homozygous	109669543
19	23939364	23939365	A	C	13	GENIC	homozygous	109669547
19	23940693	23940694	C	T	17	GENIC	homozygous	109669549
19	23940883	23940884	C	T	17	GENIC	homozygous	109669551
19	23941205	23941206	C	T	21	GENIC	homozygous	109669553
19	23941343	23941344	A	T	18	GENIC	homozygous	109669555
19	23941661	23941662	T	C	23	GENIC	homozygous	109669557
19	23942062	23942063	T	C	22	GENIC	homozygous	109669559
19	23942823	23942824	T	C	14	GENIC	homozygous	109864997
19	23942832	23942833	A	G	14	GENIC	homozygous	119602135
19	23945842	23945843	C	T	22	GENIC	homozygous	109669567
19	23943973	23943974	T	C	20	GENIC	homozygous	109669563
19	23945064	23945065	G	C	23	GENIC	homozygous	109669565
19	23946287	23946288	A	T	19	GENIC	homozygous	109669569
19	23946400	23946401	G	T	14	GENIC	homozygous	109669571
19	23946526	23946527	T	C	4	GENIC	homozygous	109802411
19	23946818	23946819	G	A	16	GENIC	homozygous	109802413