chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	44182398	44182399	T	C	47	GENIC	homozygous	114611984
13	44182406	44182407	G	C	43	GENIC	homozygous	114611985
13	44182430	44182431	T	C	27	GENIC	homozygous	114922911
13	44182718	44182719	A	C	16	GENIC	homozygous	114611987
13	44182737	44182738	C	A	24	GENIC	homozygous	114545641
13	44233320	44233321	T	C	5	GENIC	homozygous	118449708
13	44245209	44245210	C	G	25	GENIC	homozygous	114545873
13	44245210	44245211	T	A	25	GENIC	homozygous	114545875
13	44245211	44245212	C	G	25	GENIC	homozygous	114545877
13	44245500	44245501	G	T	23	GENIC	homozygous	114334657
13	44245610	44245611	C	T	29	GENIC	homozygous	114545883
13	44245686	44245687	G	T	29	GENIC	homozygous	114857366
13	44245800	44245801	C	A	34	GENIC	homozygous	114334659
13	44245881	44245882	C	T	29	GENIC	homozygous	114334665
13	44245954	44245955	A	C	34	GENIC	homozygous	114665208
13	44245965	44245966	G	C	41	GENIC	homozygous	114665210
13	44245977	44245978	T	C	38	GENIC	homozygous	114665212
13	44245986	44245987	A	C	34	GENIC	homozygous	114334667
13	44245993	44245994	G	C	33	GENIC	homozygous	114665214
13	44245995	44245996	A	C	31	GENIC	homozygous	114665216
13	44246003	44246004	A	C	37	GENIC	homozygous	114665218
13	44249778	44249779	A	T	20	GENIC	homozygous	118449709
13	44258807	44258808	T	A	32	GENIC	homozygous	114334669
13	44261159	44261160	C	T	38	GENIC	heterozygous	118598031
13	44267878	44267879	A	G	17	GENIC	homozygous	115024681
13	44267881	44267882	G	A	17	GENIC	homozygous	118449710
13	44267885	44267886	A	C	17	GENIC	homozygous	115024682
13	44268214	44268215	T	A	23	GENIC	homozygous	118449711
13	44268706	44268707	G	A	11	GENIC	homozygous	118449715
13	44275129	44275130	C	A	40	GENIC	homozygous	114665222
13	44275131	44275132	C	A	42	GENIC	homozygous	114665224
13	44293336	44293337	C	T	39	GENIC	homozygous	114665228
13	44293440	44293441	C	A	28	GENIC	homozygous	114334675
13	44293778	44293779	A	G	81	GENIC	heterozygous	118598033
13	44337915	44337916	T	C	11	GENIC	homozygous	114719489