chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	127093103	127093104	A	G	14	GENIC	homozygous	142766282
X	127095791	127095792	T	C	10	GENIC	homozygous	140702743
X	127102241	127102242	T	A	10	GENIC	homozygous	142766283
X	127103385	127103386	G	A	12	GENIC	homozygous	142766284
X	127097654	127097655	T		10	GENIC	homozygous	140597182
X	127102371	127102372	T		9	GENIC	homozygous	140597183
X	127102391	127102391		TTGTTGTT	6	GENIC	homozygous	140597184
X	127100163	127100163		T	7	GENIC	homozygous	142746625
X	127100586	127100587	A		15	GENIC	homozygous	142746626
X	127102333	127102333		TT	10	GENIC	homozygous	142746627
X	127106214	127106215	G	T	13	GENIC	homozygous	142766285
X	127106565	127106565		TA	17	GENIC	homozygous	142746629
X	127108982	127108983	A	G	8	GENIC	homozygous	142766286
X	127109880	127109881	A	G	10	GENIC	homozygous	142766287
X	127110928	127110928		AGTC	16	GENIC	homozygous	140597186
X	127112602	127112602		TA	4	GENIC	homozygous	142746630
X	127112606	127112607	G	T	3	GENIC	homozygous	142766288
X	127114447	127114448	A	T	19	GENIC	homozygous	140702748
X	127115029	127115030	C	G	16	GENIC	homozygous	140702749
X	127115143	127115144	T	C	13	GENIC	homozygous	140702750
X	127115696	127115697	A	T	15	GENIC	homozygous	140702751
X	127116439	127116440	A	C	11	GENIC	homozygous	140702753
X	127117147	127117148	C	T	8	GENIC	homozygous	140702755
X	127117604	127117605	C	T	9	GENIC	homozygous	140702756
X	127117828	127117832	TTTC		15	GENIC	homozygous	142746631
X	127121643	127121644	T	G	9	GENIC	possibly homozygous	140702760
X	127128376	127128378	CT		5	GENIC	homozygous	142746632
X	127128479	127128480	G	A	9	GENIC	homozygous	140702762
X	127132623	127132623		T	11	GENIC	homozygous	140597187
X	127138814	127138815	A	G	13	GENIC	homozygous	140702766
X	127139427	127139428	G	A	9	GENIC	homozygous	140702767