chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
49233006
49233007
T
C
43
GENIC
homozygous
117253744
10
49234949
49234956
CCGGTTT
22
GENIC
homozygous
131093185
10
49238713
49238714
C
T
37
GENIC
homozygous
117253746
10
49238927
49238927
CCAAGGAAGACGGATTGTTTGCTTTGCAGTTTAGGAAGGATCTTGGT
39
GENIC
homozygous
131093191
10
49240489
49240489
CTCTCTGT
13
GENIC
homozygous
131093192
10
49241190
49241191
G
A
35
GENIC
homozygous
116882111
10
49242022
49242023
C
A
34
GENIC
homozygous
116882115
10
49239487
49239488
T
A
23
GENIC
homozygous
118083210
10
49242829
49242831
AG
30
GENIC
homozygous
132145339
10
49243120
49243121
A
G
37
GENIC
homozygous
117129709
10
49244947
49244948
C
T
27
GENIC
homozygous
117253748
10
49245106
49245107
C
T
33
GENIC
homozygous
117253750
10
49246576
49246577
T
C
50
GENIC
homozygous
117253752
10
49246931
49246934
CCC
36
GENIC
homozygous
131093197
10
49247131
49247132
A
G
47
GENIC
homozygous
116882183
10
49247672
49247673
A
G
44
GENIC
homozygous
116882191
10
49248280
49248281
T
C
55
GENIC
homozygous
116882201
10
49248727
49248728
T
C
48
GENIC
homozygous
116882207
10
49249584
49249585
T
C
59
GENIC
homozygous
116882213
10
49250210
49250211
A
T
56
GENIC
homozygous
117253754
10
49250795
49250796
C
T
39
GENIC
homozygous
117253756
10
49250919
49250920
A
G
46
GENIC
homozygous
116882220
10
49251178
49251182
TTTT
31
GENIC
homozygous
133680379
10
49252442
49252443
A
G
42
GENIC
homozygous
116882222
10
49252939
49252940
A
G
8
GENIC
homozygous
116882224
10
49253686
49253687
C
A
42
GENIC
homozygous
117253758
10
49254312
49254313
G
A
40
GENIC
homozygous
117253760
10
49254646
49254647
T
A
55
GENIC
homozygous
117253762