chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
15
51022066
51022067
G
GAA
9
GENIC
homozygous
49052523
15
51022067
51022068
G
GGA
9
GENIC
homozygous
49052525
15
51023132
51023133
T
C
41
GENIC
homozygous
48306371
15
51023964
51023965
T
C
26
GENIC
homozygous
48306372
15
51023967
51023968
T
C
26
GENIC
homozygous
48306373
15
51024584
51024585
G
A
17
GENIC
possibly homozygous
48306374
15
51024788
51024789
G
A
24
GENIC
homozygous
48306375
15
51024862
51024863
T
C
28
GENIC
homozygous
48306376
15
51024922
51024923
C
T
39
GENIC
homozygous
48306377
15
51024930
51024931
G
T
39
GENIC
homozygous
48306378
15
51025161
51025162
T
C
45
GENIC
homozygous
48306379
15
51025398
51025399
T
TTTGC
23
GENIC
homozygous
48306380
15
51025615
51025616
C
T
23
GENIC
homozygous
48306381
15
51025641
51025642
A
G
17
GENIC
homozygous
48306382
15
51025942
51025943
C
G
16
GENIC
homozygous
48306383
15
51025952
51025953
G
A
16
GENIC
homozygous
48306384
15
51026084
51026085
G
T
21
GENIC
homozygous
48306385
15
51026302
51026303
G
GCTGGAGATAC
28
GENIC
homozygous
48306386
15
51026373
51026374
G
C
28
GENIC
homozygous
48306387
15
51026444
51026445
C
T
27
GENIC
homozygous
48306388
15
51026954
51026994
GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA
----------------------------------------
13
GENIC
homozygous
49052527
15
51028409
51028410
G
A
24
GENIC
homozygous
48306389
15
51028662
51028663
A
G
21
GENIC
homozygous
48306390
15
51029570
51029571
T
C
25
GENIC
homozygous
48306391
15
51029641
51029642
T
C
28
GENIC
homozygous
48306392
15
51029711
51029712
C
T
16
GENIC
homozygous
48306393
15
51029785
51029789
GTGT
----
1
GENIC
homozygous
49052529
15
51030773
51030774
C
T
15
GENIC
homozygous
48306394
15
51030790
51030791
T
C
17
GENIC
homozygous
48306395
15
51031633
51031634
A
T
26
GENIC
homozygous
48306396
15
51032063
51032064
T
G
26
GENIC
homozygous
48306397