chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	40555627	40555628	C	T	29	GENIC	homozygous	110329405
18	40558359	40558360	A	G	34	GENIC	homozygous	110329407
18	40559256	40559257	T	G	18	GENIC	heterozygous	110329409
18	40559778	40559779	C	T	51	GENIC	homozygous	110329411
18	40559847	40559848	T	C	44	GENIC	homozygous	110329413
18	40560060	40560061	G	A	51	GENIC	homozygous	110329415
18	40560298	40560299	T	A	32	GENIC	homozygous	110329417
18	40562042	40562043	T	C	34	GENIC	homozygous	110329419
18	40562227	40562228	T	A	52	GENIC	homozygous	110329421
18	40562510	40562511	A	T	32	GENIC	possibly homozygous	110329423
18	40564262	40564263	G	A	45	GENIC	homozygous	110329425
18	40564683	40564684	A	G	45	GENIC	homozygous	110329427
18	40566469	40566470	C	T	43	GENIC	homozygous	110329429
18	40566487	40566488	G	C	46	GENIC	homozygous	110329431
18	40567188	40567189	G	A	45	GENIC	homozygous	110329433
18	40567682	40567683	C	T	37	GENIC	homozygous	110329435
18	40568126	40568127	C	A	43	GENIC	homozygous	110329437
18	40570426	40570427	G	A	30	GENIC	homozygous	110329439
18	40570429	40570430	G	A	31	GENIC	homozygous	110329441
18	40570451	40570452	C	T	29	GENIC	homozygous	110329443
18	40570454	40570455	C	A	30	GENIC	homozygous	110329445
18	40570495	40570496	C	T	32	GENIC	homozygous	110329447
18	40571240	40571241	T	C	50	GENIC	possibly homozygous	110329449
18	40572211	40572212	A	G	48	GENIC	homozygous	110329453
18	40572535	40572536	A	G	26	GENIC	homozygous	110329455
18	40571559	40571560	C	A	7	GENIC	possibly homozygous	110684245