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	11	GENIC	homozygous	110379361
18	63017635	63017636	G	T	25	GENIC	homozygous	110379363
18	63017806	63017807	C	T	31	GENIC	homozygous	110379365
18	63018000	63018001	T	C	17	GENIC	homozygous	110379367
18	63018939	63018940	A	G	20	GENIC	homozygous	110484601
18	63019186	63019187	A	G	22	GENIC	homozygous	110379369
18	63019298	63019299	A	G	21	GENIC	homozygous	110379371
18	63020805	63020806	C	T	16	GENIC	homozygous	110379373
18	63021157	63021158	A	C	11	GENIC	homozygous	110484603
18	63022362	63022363	A	G	18	GENIC	homozygous	110379377
18	63022363	63022364	T	G	18	GENIC	homozygous	110379379
18	63028222	63028223	A	C	12	GENIC	homozygous	110379381
18	63036486	63036487	A	G	16	GENIC	homozygous	110379383
18	63037686	63037687	C	G	20	GENIC	homozygous	110379385
18	63038422	63038423	A	G	9	GENIC	homozygous	110484607
18	63041166	63041167	A	T	2	GENIC	homozygous	110703799
18	63042424	63042425	A	C	7	GENIC	homozygous	110379387
18	63044394	63044395	A	G	33	GENIC	homozygous	110379391
18	63044395	63044396	G	A	32	GENIC	homozygous	110379393
18	63046250	63046251	C	T	11	GENIC	homozygous	110379395
18	63046502	63046503	T	C	11	GENIC	homozygous	110379397
18	63046661	63046662	C	A	28	GENIC	homozygous	110379399
18	63046677	63046678	T	G	31	GENIC	homozygous	110379401
18	63046690	63046691	A	C	34	GENIC	homozygous	110379403
18	63047006	63047007	G	A	31	GENIC	homozygous	110379407
18	63047358	63047359	G	A	16	GENIC	homozygous	110379409
18	63047752	63047753	T	C	18	GENIC	homozygous	110379411
18	63048200	63048201	G	T	13	GENIC	homozygous	110379413