chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
13
51569350
51569351
T
C
68
GENIC
homozygous
114343549
13
51570359
51570493
CACACACTCACACAGGGCAGGAGAATGGGGAACACACACACACATCAAACCACACCACACACACACACACACACACACACACATACACGGGGCAGGAGAATGGGGGAACACACACACACACACACACACACACA
31
GENIC
homozygous
131126565
13
51571617
51571617
TGTG
30
GENIC
homozygous
131126566
13
51572378
51572379
G
A
63
GENIC
homozygous
114948175
13
51570955
51570956
G
T
51
GENIC
homozygous
114948165
13
51571484
51571485
G
T
42
GENIC
homozygous
114948167
13
51571700
51571701
G
A
35
GENIC
homozygous
114948171
13
51571801
51571802
A
G
44
GENIC
homozygous
114948173
13
51571522
51571522
TGTA
38
GENIC
homozygous
129053244
13
51572704
51572705
T
C
55
GENIC
homozygous
114948177
13
51572797
51572798
C
T
71
GENIC
homozygous
114948179
13
51572840
51572841
C
T
78
GENIC
homozygous
114948181
13
51572967
51572968
C
T
75
GENIC
homozygous
114948183
13
51573243
51573244
A
G
84
GENIC
homozygous
114948185
13
51573704
51573705
C
T
57
GENIC
homozygous
114948187
13
51576190
51576190
A
32
GENIC
possibly homozygous
131126567
13
51576416
51576417
T
C
59
GENIC
homozygous
114343551
13
51577010
51577011
T
C
51
GENIC
homozygous
114343553
13
51577397
51577398
C
T
50
GENIC
homozygous
114948189
13
51577537
51577538
C
T
54
GENIC
homozygous
114948191
