chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	56017001	56017002	A	G	21	GENIC	homozygous	109766717
2	56019745	56019746	G	T	48	GENIC	homozygous	109766719
2	56022208	56022209	C	T	36	GENIC	homozygous	109766721
2	56025676	56025677	G	T	19	GENIC	homozygous	109766723
2	56025990	56025991	A	T	12	GENIC	homozygous	109766725
2	56028725	56028726	G	A	43	GENIC	homozygous	109766731
2	56029450	56029451	C	T	28	GENIC	homozygous	109766733
2	56030421	56030422	T	G	22	GENIC	homozygous	109766735
2	56030422	56030423	C	G	21	GENIC	homozygous	109766737
2	56032159	56032160	C	T	23	GENIC	homozygous	110532349
2	56038821	56038822	A	G	33	GENIC	homozygous	109766741
2	56047883	56047884	G	A	28	GENIC	homozygous	109766743
2	56049181	56049182	C	T	15	GENIC	homozygous	109766745
2	56056639	56056640	A	T	37	GENIC	homozygous	109766747
2	56057409	56057410	G	C	16	GENIC	homozygous	109766749
2	56063664	56063665	T	A	12	GENIC	homozygous	109766750
2	56064130	56064131	C	T	15	GENIC	homozygous	109766752
2	56067450	56067451	A	G	27	GENIC	homozygous	109766754
2	56068367	56068368	C	T	28	GENIC	homozygous	109766756
2	56069410	56069411	A	G	30	GENIC	homozygous	109766758
2	56071901	56071902	C	T	41	GENIC	homozygous	109766760
2	56075868	56075869	A	G	33	GENIC	homozygous	109766762
2	56079112	56079113	T	C	27	GENIC	homozygous	109766764
2	56082376	56082377	C	T	32	GENIC	homozygous	109766766
2	56097958	56097959	G	A	40	GENIC	homozygous	109766768
2	56100779	56100780	C	T	11	GENIC	homozygous	109766770
2	56101095	56101096	G	A	19	GENIC	homozygous	109766772
2	56104597	56104598	G	C	31	GENIC	homozygous	109766774