chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	11941942	11941943	C	T	23	GENIC	homozygous	140263015
18	11942131	11942132	G	A	22	GENIC	homozygous	140263016
18	11942643	11942644	G	A	18	GENIC	homozygous	140263017
18	11942651	11942652	T	C	18	GENIC	homozygous	140263018
18	11943261	11943262	A	G	30	GENIC	homozygous	140263019
18	11943390	11943390		A	29	GENIC	homozygous	140209846
18	11943401	11943402	A	T	27	GENIC	homozygous	140263020
18	11943803	11943804	G	A	29	GENIC	homozygous	140263021
18	11944369	11944369		AAA	14	GENIC	possibly homozygous	140209847
18	11945763	11945764	A	G	18	GENIC	homozygous	140263022
18	11946651	11946652	A	C	28	GENIC	homozygous	140263023
18	11947930	11947931	C	T	20	GENIC	homozygous	140263024
18	11948278	11948279	A	G	25	GENIC	homozygous	140263025
18	11948384	11948384		C	16	GENIC	homozygous	140209848
18	11948569	11948570	A	C	13	GENIC	homozygous	140263026
18	11948778	11948779	G	A	15	GENIC	homozygous	140263027
18	11948948	11948950	AT		23	GENIC	homozygous	140209849
18	11949332	11949335	TTC		13	GENIC	homozygous	140209850
18	11949393	11949394	A	G	14	GENIC	homozygous	140263028
18	11949450	11949451	A	G	16	GENIC	homozygous	140263029
18	11949747	11949748	T		27	GENIC	homozygous	140209851
18	11950509	11950510	G	A	27	GENIC	homozygous	140263030