chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56586740	56586741	G	A	17	GENIC	possibly homozygous	110087756
19	56586894	56586895	T	G	20	GENIC	homozygous	109739084
19	56587590	56587591	T	G	8	GENIC	heterozygous	110087758
19	56588341	56588342	A	C	21	GENIC	heterozygous	110087760
19	56590694	56590695	T	C	20	GENIC	homozygous	109739092
19	56590759	56590760	G	A	26	GENIC	homozygous	110087762
19	56592468	56592469	T	C	15	GENIC	homozygous	109825814
19	56595514	56595515	C	T	5	GENIC	homozygous	110087764
19	56595520	56595521	A	G	4	GENIC	homozygous	110087766
19	56599098	56599099	A	G	24	GENIC	homozygous	110087768
19	56589216	56589217	G	A	10	GENIC	homozygous	109944016
19	56593662	56593663	C	T	17	GENIC	homozygous	109944018
19	56602883	56602884	A	G	32	GENIC	homozygous	109739102
19	56603521	56603522	C	T	15	GENIC	homozygous	109944024
19	56603657	56603658	T	C	10	GENIC	homozygous	109944026
19	56603967	56603968	T	G	15	GENIC	homozygous	110087770
19	56608085	56608086	A	C	27	GENIC	homozygous	109944034
19	56609226	56609227	C	G	20	GENIC	homozygous	109944036
19	56609279	56609280	G	A	27	GENIC	homozygous	110087772
19	56609326	56609327	C	T	10	GENIC	homozygous	109944038
19	56610259	56610260	C	G	15	GENIC	homozygous	110087774
19	56610588	56610589	G	A	22	GENIC	homozygous	110087776
19	56610696	56610697	C	T	20	GENIC	homozygous	109944040
19	56612446	56612447	G	A	18	GENIC	homozygous	109944042