chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
46412164
46412165
C
T
17
GENIC
homozygous
142240074
10
46416682
46416683
G
A
20
GENIC
homozygous
138784851
10
46418198
46418199
A
G
21
GENIC
homozygous
138784852
10
46419273
46419274
T
C
20
GENIC
homozygous
138784853
10
46421863
46421864
G
A
32
GENIC
homozygous
138784854
10
46425752
46425753
A
G
20
GENIC
homozygous
142240075
10
46425911
46425912
C
T
27
GENIC
homozygous
138784856
10
46426714
46426715
A
T
19
GENIC
homozygous
138784857
10
46427689
46427690
A
T
29
GENIC
homozygous
138784860
10
46430298
46430299
T
C
26
GENIC
homozygous
138784861
10
46433369
46433370
C
A
16
GENIC
homozygous
138784865
10
46433930
46433931
A
G
17
GENIC
homozygous
138784866
10
46435987
46435988
A
14
GENIC
homozygous
138682346
10
46433688
46433688
T
15
GENIC
homozygous
142201726
10
46425165
46425166
T
15
GENIC
homozygous
138682341
10
46425167
46425196
TCTCTCTCTCTCTCTCTCTCTCTCTCTCT
16
GENIC
homozygous
138682342
10
46429907
46429907
A
20
GENIC
possibly homozygous
138682344
10
46437491
46437492
G
A
26
GENIC
possibly homozygous
142240076
10
46442806
46442807
T
C
17
GENIC
homozygous
138784868
10
46444161
46444162
T
G
25
GENIC
homozygous
138784869
