chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	57038223	57038224	C	T	44	GENIC	homozygous	110544299
18	57039874	57039875	G	A	42	GENIC	homozygous	110363599
18	57040442	57040443	A	G	33	GENIC	possibly homozygous	110363601
18	57042113	57042114	A	G	31	GENIC	homozygous	110363603
18	57042421	57042422	T	C	35	GENIC	possibly homozygous	110544301
18	57042723	57042724	C	T	47	GENIC	homozygous	110544303
18	57043180	57043181	C	T	31	GENIC	homozygous	110544305
18	57043189	57043190	T	A	30	GENIC	homozygous	110363611
18	57043239	57043240	G	A	34	GENIC	homozygous	110544307
18	57043248	57043249	T	A	31	GENIC	homozygous	110544309
18	57043317	57043318	C	T	49	GENIC	possibly homozygous	110544311
18	57043335	57043336	C	T	44	GENIC	possibly homozygous	110544313
18	57043372	57043373	A	T	51	GENIC	possibly homozygous	110363616
18	57044880	57044881	T	A	28	GENIC	homozygous	110544315
18	57047752	57047753	G	A	48	GENIC	homozygous	110363630
18	57047781	57047782	T	C	43	GENIC	homozygous	110363632
18	57048164	57048165	A	G	49	GENIC	possibly homozygous	110363636
18	57048595	57048596	A	G	51	GENIC	possibly homozygous	110363638
18	57049344	57049345	T	C	56	GENIC	homozygous	110544317
18	57049490	57049491	C	T	56	GENIC	homozygous	110363640
18	57050048	57050049	G	C	16	GENIC	homozygous	110544319
18	57043426	57043427	T	A	66	GENIC	possibly homozygous	110813814