chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	63017244	63017245	C	T	10	GENIC	homozygous	110379359
18	63017536	63017537	C	T	18	GENIC	homozygous	110379361
18	63017635	63017636	G	T	20	GENIC	homozygous	110379363
18	63017806	63017807	C	T	24	GENIC	homozygous	110379365
18	63018000	63018001	T	C	24	GENIC	homozygous	110379367
18	63018939	63018940	A	G	29	GENIC	homozygous	110484601
18	63019186	63019187	A	G	30	GENIC	homozygous	110379369
18	63019298	63019299	A	G	21	GENIC	homozygous	110379371
18	63020805	63020806	C	T	17	GENIC	homozygous	110379373
18	63022362	63022363	A	G	17	GENIC	homozygous	110379377
18	63022363	63022364	T	G	18	GENIC	homozygous	110379379
18	63028222	63028223	A	C	17	GENIC	homozygous	110379381
18	63036486	63036487	A	G	13	GENIC	homozygous	110379383
18	63038422	63038423	A	G	14	GENIC	homozygous	110484607
18	63042424	63042425	A	C	7	GENIC	homozygous	110379387
18	63043336	63043337	T	C	22	GENIC	homozygous	110379389
18	63044394	63044395	A	G	23	GENIC	homozygous	110379391
18	63044395	63044396	G	A	25	GENIC	homozygous	110379393
18	63046502	63046503	T	C	14	GENIC	homozygous	110379397
18	63046661	63046662	C	A	25	GENIC	homozygous	110379399
18	63046677	63046678	T	G	27	GENIC	homozygous	110379401
18	63046690	63046691	A	C	25	GENIC	homozygous	110379403
18	63046691	63046692	G	C	25	GENIC	homozygous	110379405
18	63047006	63047007	G	A	24	GENIC	homozygous	110379407
18	63047752	63047753	T	C	14	GENIC	homozygous	110379411
18	63048200	63048201	G	T	17	GENIC	possibly homozygous	110379413