chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
130163184
130163185
G
A
15
GENIC
homozygous
115889428
7
130163533
130163534
C
T
10
GENIC
homozygous
115889430
7
130164645
130164646
G
A
10
GENIC
homozygous
115889432
7
130164959
130164960
C
T
20
GENIC
homozygous
115889434
7
130165072
130165073
A
G
22
GENIC
homozygous
115889436
7
130165673
130165674
C
T
19
GENIC
homozygous
115889438
7
130166631
130166632
A
G
15
GENIC
homozygous
115889440
7
130167383
130167384
T
C
27
GENIC
homozygous
115889442
7
130168166
130168167
C
T
31
GENIC
homozygous
115889444
7
130168523
130168524
A
C
14
GENIC
homozygous
115889446
7
130169700
130169701
G
T
16
GENIC
possibly homozygous
115889448
7
130170169
130170170
A
G
16
GENIC
homozygous
115889450
7
130171669
130171670
A
G
8
GENIC
homozygous
115889454
7
130171758
130171759
C
G
17
GENIC
homozygous
115889456
7
130172963
130172964
G
A
18
GENIC
homozygous
115889458
7
130173038
130173039
G
A
21
GENIC
homozygous
115889460
7
130173709
130173710
A
G
21
GENIC
homozygous
115889462
7
130170750
130170750
ATG
20
GENIC
homozygous
128520228
7
130170704
130170704
CAGTGCTCAC
24
GENIC
homozygous
128520226
7
130170748
130170748
T
21
GENIC
homozygous
128520227
7
130171591
130171591
C
8
GENIC
homozygous
128520229
7
130175684
130175684
A
16
GENIC
homozygous
128520230
7
130176424
130176425
C
T
13
GENIC
homozygous
115889464
7
130177396
130177397
T
C
21
GENIC
homozygous
115889466
7
130177548
130177549
C
T
19
GENIC
homozygous
115889468
7
130178013
130178014
A
G
14
GENIC
homozygous
115889470
7
130175050
130175051
A
15
GENIC
homozygous
131024522
7
130175056
130175206
TAAGATTTATTTTATTAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCCCAAAAAAAAGTCTCCCAAGCAAAAAATAAATAAATAAAAAAGTAG
12
GENIC
heterozygous
132112633
7
130178017
130178018
T
C
14
GENIC
homozygous
115889472
7
130178243
130178244
T
C
10
GENIC
homozygous
115889474
7
130178249
130178250
T
G
11
GENIC
homozygous
115889476
