chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	55297783	55297784	T	C	22	GENIC	possibly homozygous	52641388
8	55298237	55298238	A	G	5	GENIC	heterozygous	52641390
8	55298954	55298955	A	T	16	GENIC	homozygous	52641392
8	55299296	55299297	C	CCTCT	6	GENIC	heterozygous	53582517
8	55299710	55299711	C	CTCAT	4	GENIC	heterozygous	52641400
8	55301439	55301440	A	AAATAAACCTTTCCTCCTTTTAAGTTTCTGACTTCAGGCAATTTGTCATAGTAACAGAAAGC	9	GENIC	heterozygous	53387720
8	55302214	55302215	T	TTC	17	GENIC	possibly homozygous	52641412
8	55302557	55302558	A	G	8	GENIC	possibly homozygous	52641414
8	55303159	55303160	T	C	11	GENIC	possibly homozygous	52641416
8	55303336	55303337	C	T	4	GENIC	heterozygous	52641418
8	55304037	55304038	C	G	19	GENIC	possibly homozygous	52641420
8	55305599	55305600	G	GT	6	GENIC	heterozygous	52641426
8	55306328	55306329	A	T	4	GENIC	heterozygous	52641428
8	55306693	55306694	T	C	5	GENIC	heterozygous	52641432
8	55307071	55307072	C	A	1	GENIC	homozygous	52641470
8	55307073	55307074	T	A	1	GENIC	homozygous	52641472
8	55308083	55308084	T	-	1	GENIC	homozygous	52641477
8	55308240	55308241	C	G	7	GENIC	homozygous	52641479
8	55308954	55308955	T	C	8	GENIC	homozygous	52641481
8	55309165	55309166	G	C	9	GENIC	heterozygous	52641483
8	55311039	55311040	G	A	13	GENIC	homozygous	52641485
8	55312142	55312143	C	T	11	GENIC	possibly homozygous	52641487
8	55312282	55312283	C	G	24	GENIC	homozygous	52641489
8	55312455	55312456	G	T	14	GENIC	possibly homozygous	52641491
8	55313159	55313160	T	C	11	GENIC	heterozygous	52641493
8	55313230	55313231	A	C	11	GENIC	possibly homozygous	52641495
8	55317201	55317202	T	G	22	GENIC	possibly homozygous	52641497
8	55317971	55317972	G	-	2	GENIC	heterozygous	52978110
8	55325439	55325440	G	T	6	GENIC	homozygous	52978135
8	55325440	55325441	T	A	6	GENIC	homozygous	52978136