chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10615207	10615208	C	A	26	GENIC	homozygous	143721350
20	10615482	10615483	T	C	17	GENIC	homozygous	143721351
20	10615591	10615592	G	A	17	GENIC	homozygous	143721352
20	10617082	10617083	A	G	3	GENIC	homozygous	130052772
20	10617203	10617204	A	G	16	GENIC	homozygous	130052773
20	10617632	10617633	A		18	GENIC	homozygous	143710888
20	10617812	10617813	G	A	19	GENIC	homozygous	143721353
20	10617841	10617842	G	A	18	GENIC	homozygous	143721354
20	10618491	10618492	T	C	18	GENIC	homozygous	143721355
20	10618501	10618502	T	C	20	GENIC	homozygous	143721356
20	10618904	10618904		AA	12	GENIC	homozygous	143710889
20	10622434	10622435	G	A	17	GENIC	homozygous	130052775
20	10622762	10622763	T	C	26	GENIC	homozygous	130052776
20	10623015	10623016	G	A	15	GENIC	homozygous	130052777
20	10623569	10623570	T	C	7	GENIC	homozygous	130052778
20	10623878	10623879	G	A	13	GENIC	homozygous	130052779
20	10624624	10624625	G	A	17	GENIC	homozygous	130052780
20	10624872	10624873	C	T	23	GENIC	homozygous	143721357
20	10624961	10624962	A	T	23	GENIC	homozygous	155136201
20	10618204	10618205	G		27	GENIC	homozygous	403754131
20	10618204	10618205	G	C	27	GENIC	heterozygous	403754132
20	10624961	10624962	A		23	GENIC	heterozygous	403754133
20	10625028	10625029	C	T	26	GENIC	homozygous	130052781
20	10625376	10625377	C	T	21	GENIC	homozygous	143721358
20	10626429	10626430	C	A	14	GENIC	homozygous	130052784
20	10626452	10626453	G	T	13	GENIC	homozygous	143721359
20	10626831	10626832	T	C	17	GENIC	homozygous	130052785
20	10627613	10627614	G	A	22	GENIC	homozygous	143721360
20	10627778	10627779	T	A	21	GENIC	homozygous	130052786
20	10628708	10628709	T	C	24	GENIC	homozygous	130052787