chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
111800543
111800544
T
A
33
GENIC
heterozygous
130202199
X
111800550
111800551
G
A
35
GENIC
heterozygous
130202200
X
111800573
111800574
C
T
34
GENIC
heterozygous
130202201
X
111800574
111800575
C
T
34
GENIC
heterozygous
130202202
X
111800577
111800578
G
C
34
GENIC
heterozygous
130202203
X
111800589
111800590
C
T
34
GENIC
heterozygous
130202204
X
111800660
111800661
A
C
27
GENIC
heterozygous
120059955
X
111800774
111800775
A
T
14
GENIC
heterozygous
132439214
X
111800780
111800781
C
A
12
GENIC
heterozygous
132439215
X
111800793
111800794
G
A
10
GENIC
heterozygous
132439216
X
111800802
111800803
G
T
11
GENIC
heterozygous
132439217
X
111800812
111800813
T
G
13
GENIC
heterozygous
120059959
X
111800958
111800959
T
G
27
GENIC
heterozygous
120714708
X
111800967
111800968
C
T
24
GENIC
heterozygous
131248946
X
111801081
111801082
A
G
22
GENIC
heterozygous
130202206
X
111800832
111800833
G
A
19
GENIC
heterozygous
134472845
X
111800834
111800835
A
G
19
GENIC
heterozygous
134472846
X
111800978
111800979
G
T
20
GENIC
heterozygous
134472847
X
111801007
111801008
G
A
20
GENIC
heterozygous
134472848
X
111801088
111801122
TCCTCTTTCTCCACATCCTCTTCAGCACCTGCTG
26
GENIC
heterozygous
133985627
X
111801189
111801190
G
A
17
GENIC
heterozygous
131566926