chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	81700501	81700502	A	G	36	GENIC	homozygous	110422271
18	81705774	81705775	G	A	27	GENIC	homozygous	110422273
18	81706056	81706057	T	C	28	GENIC	homozygous	110422275
18	81706641	81706642	G	T	23	GENIC	homozygous	110422277
18	81709487	81709488	C	T	32	GENIC	homozygous	110422279
18	81709693	81709694	T	C	25	GENIC	homozygous	110422281
18	81716089	81716090	G	T	33	GENIC	homozygous	110422283
18	81716904	81716905	A	G	16	GENIC	homozygous	110422287
18	81723844	81723845	C	T	26	GENIC	homozygous	110422289
18	81724289	81724290	C	G	28	GENIC	homozygous	110422291
18	81724929	81724930	A	C	21	GENIC	homozygous	110422293
18	81726124	81726125	A	G	17	GENIC	homozygous	110501248
18	81726125	81726126	C	A	16	GENIC	homozygous	110422295
18	81726171	81726172	T	A	16	GENIC	homozygous	110501250
18	81726180	81726181	C	A	11	GENIC	homozygous	110501252
18	81726265	81726266	T	G	19	GENIC	homozygous	110422297
18	81726280	81726281	A	G	20	GENIC	homozygous	110422299
18	81726281	81726282	G	A	20	GENIC	homozygous	110422301
18	81726288	81726289	G	A	21	GENIC	homozygous	110422303
18	81726291	81726292	G	C	21	GENIC	homozygous	110422305
18	81726296	81726297	C	A	22	GENIC	homozygous	110422307