chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4966938	4966939	T	C	27	GENIC	homozygous	109419634
20	4967617	4967618	T	C	36	GENIC	homozygous	109296503
20	4968142	4968143	A	G	32	GENIC	homozygous	109419636
20	4968279	4968280	T	A	22	GENIC	homozygous	109463115
20	4968283	4968284	T	A	22	GENIC	homozygous	109419638
20	4968287	4968288	T	A	22	GENIC	homozygous	109419640
20	4968291	4968292	T	A	22	GENIC	homozygous	109419642
20	4968650	4968651	T	C	41	GENIC	homozygous	109296505
20	4968899	4968900	A	G	21	GENIC	homozygous	109296507
20	4969406	4969407	A	G	9	GENIC	homozygous	109455280
20	4969461	4969462	A	G	21	GENIC	homozygous	109455282
20	4969466	4969467	C	T	22	GENIC	homozygous	109419644
20	4969497	4969498	G	A	28	GENIC	homozygous	109419646
20	4969573	4969574	A	G	26	GENIC	homozygous	109296511
20	4969599	4969600	A	G	30	GENIC	homozygous	109419648
20	4969606	4969607	T	C	31	GENIC	homozygous	109419650
20	4969620	4969621	T	C	26	GENIC	homozygous	109419652
20	4969702	4969703	A	G	35	GENIC	homozygous	109419654
20	4969749	4969750	C	G	42	GENIC	homozygous	109419656
20	4969880	4969881	A	G	22	GENIC	homozygous	109419657
20	4970428	4970429	C	T	43	GENIC	homozygous	109419659
20	4970497	4970498	T	C	38	GENIC	homozygous	109419661