chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10615207	10615208	C	A	41	GENIC	possibly homozygous	143721350
20	10615482	10615483	T	C	31	GENIC	homozygous	143721351
20	10615591	10615592	G	A	37	GENIC	homozygous	143721352
20	10616992	10616993	G		17	GENIC	homozygous	403464132
20	10616992	10616993	G	A	17	GENIC	heterozygous	403464133
20	10617082	10617083	A	G	10	GENIC	homozygous	130052772
20	10617203	10617204	A	G	39	GENIC	homozygous	130052773
20	10617812	10617813	G	A	47	GENIC	homozygous	143721353
20	10617841	10617842	G	A	50	GENIC	homozygous	143721354
20	10618491	10618492	T	C	40	GENIC	homozygous	143721355
20	10618501	10618502	T	C	41	GENIC	homozygous	143721356
20	10622434	10622435	G	A	59	GENIC	homozygous	130052775
20	10622762	10622763	T	C	52	GENIC	homozygous	130052776
20	10623015	10623016	G	A	58	GENIC	homozygous	130052777
20	10623569	10623570	T	C	35	GENIC	homozygous	130052778
20	10623878	10623879	G	A	55	GENIC	homozygous	130052779
20	10624624	10624625	G	A	38	GENIC	homozygous	130052780
20	10624872	10624873	C	T	46	GENIC	homozygous	143721357
20	10624961	10624962	A	T	34	GENIC	possibly homozygous	155136201
20	10625028	10625029	C	T	44	GENIC	homozygous	130052781
20	10625376	10625377	C	T	42	GENIC	homozygous	143721358
20	10626429	10626430	C	A	40	GENIC	homozygous	130052784
20	10626452	10626453	G	T	36	GENIC	homozygous	143721359
20	10626831	10626832	T	C	41	GENIC	homozygous	130052785
20	10627613	10627614	G	A	47	GENIC	homozygous	143721360
20	10627778	10627779	T	A	45	GENIC	homozygous	130052786
20	10628708	10628709	T	C	51	GENIC	homozygous	130052787
20	10624961	10624962	A		34	GENIC	heterozygous	403754133
20	10618204	10618205	G		43	GENIC	homozygous	403754131
20	10618204	10618205	G	C	43	GENIC	heterozygous	403754132
20	10618904	10618904		AA	27	GENIC	homozygous	143710889
20	10624959	10624959		T	33	GENIC	heterozygous	129982940
20	10617632	10617633	A		30	GENIC	homozygous	143710888