chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	221504177	221504179	GT	--	37	GENIC	homozygous	61094030
1	221504555	221504556	G	A	22	GENIC	homozygous	61094031
1	221505977	221505978	C	T	47	GENIC	homozygous	61094032
1	221508190	221508191	C	T	31	GENIC	homozygous	61094033
1	221509246	221509247	C	T	20	GENIC	homozygous	61094034
1	221509655	221509656	G	A	37	GENIC	possibly homozygous	61094035
1	221509690	221509691	G	A	36	GENIC	heterozygous	61321175
1	221510285	221510286	T	A	23	GENIC	homozygous	61094036
1	221511361	221511362	C	CGT	12	GENIC	heterozygous	61094037
1	221511361	221511362	C	CGTGT	12	GENIC	heterozygous	61094038
1	221511993	221511994	A	G	21	GENIC	homozygous	61094039
1	221513366	221513367	T	C	30	GENIC	homozygous	61094040
1	221514210	221514211	T	C	42	GENIC	homozygous	61094041
1	221515199	221515200	A	G	30	GENIC	homozygous	61094042
1	221515517	221515518	C	T	29	GENIC	homozygous	61094043
1	221515714	221515718	CTTT	----	10	GENIC	heterozygous	61094044
1	221515714	221515717	CTT	---	10	GENIC	heterozygous	61094045