chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	40906235	40906236	C	T	18	GENIC	homozygous	109699537
19	40906827	40906828	G	A	6	GENIC	homozygous	109699539
19	40908536	40908537	C	T	7	GENIC	homozygous	109699543
19	40908537	40908538	T	C	7	GENIC	homozygous	109699545
19	40909735	40909736	T	A	15	GENIC	homozygous	109699549
19	40909954	40909955	C	G	11	GENIC	homozygous	109699551
19	40909992	40909993	T	G	11	GENIC	homozygous	109699553
19	40910333	40910334	C	T	14	GENIC	homozygous	109699555
19	40910932	40910933	T	C	27	GENIC	homozygous	109699557
19	40911098	40911099	T	C	21	GENIC	homozygous	109699559
19	40911204	40911205	T	C	19	GENIC	homozygous	109699561
19	40911324	40911325	T	C	20	GENIC	homozygous	109699563
19	40912220	40912221	A	G	33	GENIC	homozygous	109699565
19	40912897	40912898	A	G	13	GENIC	homozygous	109699567
19	40913200	40913201	C	T	18	GENIC	homozygous	109781291
19	40913354	40913355	C	G	12	GENIC	homozygous	109699569
19	40913816	40913817	T	C	8	GENIC	homozygous	109699571
19	40915331	40915332	C	T	31	GENIC	homozygous	109699573
19	40916267	40916268	T	C	16	GENIC	homozygous	109699575
19	40917348	40917349	A	G	23	GENIC	homozygous	109699579
19	40918095	40918096	C	T	18	GENIC	homozygous	109699581
19	40918120	40918121	G	A	15	GENIC	homozygous	109699583
19	40918181	40918182	T	C	13	GENIC	homozygous	109699585
19	40918567	40918568	G	A	8	GENIC	homozygous	109699587
19	40919412	40919413	G	A	8	GENIC	homozygous	109699589
19	40920589	40920590	T	C	7	GENIC	homozygous	109699591
19	40920865	40920866	A	G	5	GENIC	homozygous	109699593
19	40921208	40921209	T	C	11	GENIC	homozygous	109699595
19	40921746	40921747	C	T	12	GENIC	homozygous	109699597
19	40923653	40923654	A	G	22	GENIC	homozygous	109699602