chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10734079	10734080	T	G	6	GENIC	homozygous	110076409
19	10734080	10734081	G	T	6	GENIC	homozygous	110076412
19	10734219	10734220	G	A	5	GENIC	homozygous	110076414
19	10734669	10734670	C	T	6	GENIC	homozygous	110076416
19	10736563	10736564	A	G	4	GENIC	homozygous	109634852
19	10736685	10736686	A	G	3	GENIC	homozygous	110076418
19	10736742	10736743	G	A	5	GENIC	homozygous	109634854
19	10737577	10737578	C	T	10	GENIC	homozygous	110099024
19	10738752	10738753	T	G	7	GENIC	homozygous	109634858
19	10738773	10738774	T	C	3	GENIC	homozygous	109634860
19	10739631	10739632	T	G	2	GENIC	homozygous	109634864
19	10739661	10739662	A	G	4	GENIC	homozygous	109634866
19	10740095	10740096	C	T	5	GENIC	homozygous	110076422
19	10740372	10740373	C	T	4	GENIC	homozygous	110076424
19	10740587	10740588	T	C	8	GENIC	homozygous	109634870
19	10740851	10740852	G	T	5	GENIC	homozygous	110099026
19	10740940	10740941	G	C	8	GENIC	homozygous	110076426
19	10741249	10741250	C	T	3	GENIC	homozygous	110076428
19	10741301	10741302	C	T	3	GENIC	homozygous	110076430
19	10741619	10741620	T	C	3	GENIC	homozygous	110169096
19	10741629	10741630	T	C	3	GENIC	homozygous	110169099
19	10741652	10741653	A	G	2	GENIC	homozygous	110143495
19	10741764	10741765	G	A	4	GENIC	homozygous	110076432
19	10741888	10741889	C	T	5	GENIC	homozygous	110076434
19	10741927	10741928	G	A	6	GENIC	homozygous	110076436
19	10741941	10741942	C	T	4	GENIC	homozygous	110076439
19	10742153	10742154	T	A	2	GENIC	homozygous	110076441
19	10742242	10742243	T	C	2	GENIC	homozygous	110076443
19	10742577	10742578	G	A	4	GENIC	homozygous	109634874
19	10744600	10744601	G	A	5	GENIC	homozygous	109634878
19	10746332	10746333	A	G	4	GENIC	homozygous	109634880
19	10747389	10747390	G	A	10	GENIC	homozygous	109634882
19	10751284	10751285	C	T	6	GENIC	homozygous	110076447