chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5448262	5448263	T	C	34	GENIC	homozygous	109420382
20	5448907	5448908	C	T	48	GENIC	possibly homozygous	109420386
20	5449640	5449641	G	T	46	GENIC	homozygous	109420394
20	5449904	5449905	C	T	38	GENIC	homozygous	109420396
20	5450300	5450301	G	A	24	GENIC	homozygous	109420398
20	5450404	5450405	C	A	31	GENIC	homozygous	109077998
20	5450982	5450983	C	G	54	GENIC	heterozygous	109420400
20	5450985	5450986	G	C	55	GENIC	heterozygous	109420402
20	5450986	5450987	G	A	54	GENIC	heterozygous	109420404
20	5450990	5450991	T	A	56	GENIC	heterozygous	109420406
20	5451408	5451409	C	T	42	GENIC	homozygous	109078004
20	5451428	5451429	C	T	41	GENIC	homozygous	109420410
20	5451433	5451434	T	C	41	GENIC	homozygous	109420412
20	5451435	5451436	T	C	43	GENIC	homozygous	109420414
20	5451472	5451473	G	A	40	GENIC	homozygous	109420416
20	5451520	5451521	T	C	41	GENIC	homozygous	109078006
20	5451531	5451532	C	G	47	GENIC	homozygous	109420418
20	5451756	5451757	G	A	35	GENIC	homozygous	109420420
20	5451940	5451941	A	G	51	GENIC	homozygous	109420428
20	5452253	5452254	C	T	51	GENIC	homozygous	109420438
20	5452302	5452303	A	G	51	GENIC	homozygous	109420442
20	5452732	5452733	G	A	51	GENIC	homozygous	109420448
20	5453607	5453608	A	G	32	GENIC	homozygous	109078010
20	5453690	5453691	A	G	47	GENIC	homozygous	109078012
20	5454191	5454192	G	A	40	GENIC	homozygous	109420454
20	5454206	5454207	T	C	34	GENIC	homozygous	109078028
20	5454443	5454444	A	G	30	GENIC	homozygous	109390290
20	5455019	5455020	A	G	38	GENIC	homozygous	109078032
20	5455208	5455209	C	T	25	GENIC	homozygous	109420456
20	5455349	5455350	C	T	12	GENIC	homozygous	109078034
20	5455478	5455479	G	C	14	GENIC	homozygous	109078036
20	5455619	5455620	T	C	20	GENIC	homozygous	109078038