chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
48010146
48010147
C
T
42
GENIC
homozygous
116879023
10
48014664
48014665
G
A
52
GENIC
homozygous
116588241
10
48016180
48016181
A
G
53
GENIC
homozygous
116588243
10
48017255
48017256
T
C
48
GENIC
homozygous
116588245
10
48019845
48019846
G
A
37
GENIC
homozygous
116588247
10
48022575
48022576
C
A
16
GENIC
homozygous
116774453
10
48022581
48022582
T
A
16
GENIC
homozygous
116774455
10
48023932
48023933
A
G
40
GENIC
homozygous
116879029
10
48024091
48024092
C
T
48
GENIC
homozygous
116879031
10
48024894
48024895
A
T
35
GENIC
homozygous
116588249
10
48025869
48025870
A
T
42
GENIC
homozygous
116588255
10
48028801
48028802
T
C
65
GENIC
homozygous
116588257
10
48031871
48031872
C
A
50
GENIC
homozygous
116588265
10
48032190
48032190
T
59
GENIC
homozygous
131092765
10
48032432
48032433
A
G
53
GENIC
homozygous
116588267
10
48035993
48035994
G
A
36
GENIC
homozygous
116879033
10
48041308
48041309
T
C
69
GENIC
homozygous
116588271
10
48042663
48042664
T
G
58
GENIC
possibly homozygous
116588273
10
48043915
48043916
T
A
56
GENIC
homozygous
116588275
10
48043916
48043917
T
A
55
GENIC
homozygous
116588277
10
48043917
48043918
T
A
55
GENIC
homozygous
116588279
10
48023347
48023376
TCTCTCTCTCTCTCTCTCTCTCTCTCTCT
34
GENIC
homozygous
128815028
10
48023345
48023346
T
33
GENIC
homozygous
128815027
10
48028410
48028410
A
43
GENIC
possibly homozygous
128815030
10
48034489
48034490
A
41
GENIC
possibly homozygous
128815031
