chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	22088855	22088856	G	T	25	GENIC	homozygous	112543573
4	22093480	22093481	A	C	17	GENIC	homozygous	112543579
4	22094175	22094176	A	G	28	GENIC	homozygous	112543581
4	22098808	22098809	A	G	23	GENIC	homozygous	112543585
4	22098932	22098933	A	G	18	GENIC	homozygous	112543587
4	22098991	22098992	T	G	10	GENIC	homozygous	112543589
4	22101806	22101807	T	A	15	GENIC	homozygous	112543596
4	22103129	22103130	T	C	19	GENIC	homozygous	112543600
4	22107769	22107770	C	T	24	GENIC	homozygous	112543604
4	22107925	22107926	G	A	23	GENIC	homozygous	112543606
4	22109899	22109900	G	A	22	GENIC	homozygous	112543609
4	22111915	22111916	A	G	18	GENIC	homozygous	112543611
4	22112272	22112273	A	G	16	GENIC	homozygous	112543613
4	22113504	22113505	T	C	15	GENIC	homozygous	112543615
4	22113532	22113533	A	T	16	GENIC	homozygous	112543617
4	22113759	22113760	T	C	13	GENIC	homozygous	112543619
4	22113903	22113904	G	A	13	GENIC	homozygous	112543621
4	22114365	22114366	G	C	11	GENIC	homozygous	113086517
4	22114392	22114393	G	A	12	GENIC	homozygous	112543623
4	22115508	22115509	G	A	23	GENIC	homozygous	112543627
4	22115671	22115672	T	C	11	GENIC	homozygous	112543629
4	22116188	22116189	G	T	12	GENIC	homozygous	112543631