chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	123999822	123999823	T	C	26	GENIC	heterozygous	108821152
X	123999824	123999825	A	G	26	GENIC	heterozygous	108821153
X	123999829	123999830	G	A	25	GENIC	heterozygous	108821154
X	123999916	123999917	C	T	35	GENIC	heterozygous	108424519
X	124000305	124000306	G	A	15	GENIC	heterozygous	108325454
X	124000471	124000472	G	A	21	GENIC	heterozygous	108325456
X	124000569	124000570	G	A	25	GENIC	heterozygous	108454741
X	124001414	124001415	C	G	20	GENIC	heterozygous	120011482
X	124001416	124001417	T	G	19	GENIC	heterozygous	120011483
X	124001421	124001422	C	G	17	GENIC	heterozygous	120011484
X	124001425	124001426	A	G	17	GENIC	heterozygous	120011485
X	124001459	124001460	A	G	21	GENIC	heterozygous	120011486
X	124001701	124001702	C	T	34	GENIC	heterozygous	119951402
X	124001466	124001467	C	T	21	GENIC	heterozygous	119951399
X	124001619	124001620	C	T	37	GENIC	heterozygous	119951400
X	124001633	124001634	G	T	37	GENIC	heterozygous	119951401