chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	74177354	74177355	T	C	31	GENIC	homozygous	110402434
18	74203425	74203426	C	T	24	GENIC	homozygous	119501530
18	74215178	74215179	T	C	10	GENIC	homozygous	119539536
18	74215456	74215457	A	C	21	GENIC	homozygous	110402436
18	74232134	74232135	A	C	3	GENIC	homozygous	110402438
18	74232213	74232214	G	A	20	GENIC	homozygous	110402440
18	74232332	74232333	C	A	29	GENIC	homozygous	119501531
18	74232344	74232345	G	C	30	GENIC	homozygous	110402442
18	74250538	74250539	A	G	11	GENIC	homozygous	110816147
18	74250540	74250541	A	C	10	GENIC	homozygous	119501532
18	74273616	74273617	C	T	14	GENIC	homozygous	110499744
18	74273620	74273621	G	C	12	GENIC	homozygous	110402446
18	74273622	74273623	G	C	12	GENIC	homozygous	110499746
18	74273625	74273626	A	C	12	GENIC	homozygous	110499748
18	74273642	74273643	T	A	12	GENIC	homozygous	110499750
18	74273644	74273645	G	A	12	GENIC	homozygous	110499752
18	74273646	74273647	G	C	12	GENIC	homozygous	110499754
18	74273654	74273655	C	A	13	GENIC	homozygous	110499756
18	74273657	74273658	T	A	13	GENIC	homozygous	110499758
18	74273661	74273662	G	A	13	GENIC	homozygous	110499760
18	74273663	74273664	G	A	13	GENIC	homozygous	110499762
18	74273682	74273683	C	T	21	GENIC	homozygous	110499764
18	74273864	74273865	C	T	12	GENIC	heterozygous	119569396
18	74215069	74215070	T	A	29	GENIC	possibly homozygous	110600062
18	74242015	74242016	G	T	35	GENIC	homozygous	110658522
18	74250572	74250573	T	G	10	GENIC	homozygous	110658523
18	74250574	74250575	T	G	10	GENIC	homozygous	110658525