chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
51260416
51260417
T
A
46
GENIC
homozygous
140473085
19
51261371
51261372
C
T
40
GENIC
homozygous
140473086
19
51261373
51261374
G
C
42
GENIC
homozygous
140473087
19
51261931
51261932
T
C
40
GENIC
homozygous
140473088
19
51262361
51262362
C
T
34
GENIC
homozygous
140473089
19
51262408
51262409
G
A
43
GENIC
homozygous
140473090
19
51262558
51262559
T
C
47
GENIC
homozygous
140473091
19
51262773
51262774
T
G
33
GENIC
homozygous
140473092
19
51264189
51264190
A
T
45
GENIC
possibly homozygous
140473093
19
51264422
51264423
C
T
38
GENIC
homozygous
140473094
19
51265025
51265026
T
A
34
GENIC
homozygous
140473095
19
51265651
51265652
A
G
50
GENIC
homozygous
140473096
19
51265938
51265939
A
G
40
GENIC
homozygous
140473097
19
51266119
51266120
C
T
55
GENIC
homozygous
140473098
19
51266361
51266361
AAC
40
GENIC
homozygous
140393831
19
51266482
51266482
TGCCACCGCACTGTGACATAGCACAGACAGGAG
29
GENIC
homozygous
140393832
19
51266598
51266599
G
A
33
GENIC
homozygous
140473099
19
51268118
51268123
GAGTA
52
GENIC
homozygous
140393833
19
51268387
51268387
C
58
GENIC
homozygous
140393834
19
51269159
51269160
G
T
40
GENIC
possibly homozygous
140473100
19
51269202
51269203
A
G
37
GENIC
homozygous
140473101
19
51269209
51269210
C
T
32
GENIC
homozygous
140473102
19
51269211
51269212
T
G
29
GENIC
homozygous
140473103
19
51269303
51269304
T
C
23
GENIC
homozygous
140473104
19
51269312
51269313
C
A
25
GENIC
homozygous
140473105
19
51269314
51269314
A
24
GENIC
homozygous
140393835
19
51269322
51269323
G
T
20
GENIC
homozygous
140473106
19
51269330
51269331
G
A
21
GENIC
homozygous
140473107
19
51272069
51272070
C
A
42
GENIC
homozygous
140473108
19
51273000
51273001
A
T
33
GENIC
homozygous
140473109
