chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
82595325
82595326
C
CA
5
GENIC
homozygous
62137450
1
82595346
82595347
A
G
12
GENIC
homozygous
61669581
1
82595611
82595612
T
TGTCTGTGTC
18
GENIC
homozygous
62137451
1
82595737
82595738
G
A
26
GENIC
possibly homozygous
61450171
1
82596094
82596095
C
T
19
GENIC
homozygous
61669583
1
82596122
82596123
G
GGCTCTACCACTGAGCCACGCCCCCAGCCCCTCACTGGGGGATTCTAGGCAGGGAGGA
5
GENIC
homozygous
62137452
1
82596974
82596975
G
A
23
GENIC
possibly homozygous
61450174
1
82597350
82597351
C
CGG
6
GENIC
homozygous
61669585
1
82597444
82597445
C
CCCCAGTGAGGGATTGGGGATGTGGCCCAGTGGTAGAGCCCCTGCCTAGAACCT
17
GENIC
homozygous
62137453
1
82599041
82599044
TTT
---
4
GENIC
heterozygous
61450178
1
82599042
82599044
TT
--
4
GENIC
heterozygous
61450179
1
82600087
82600088
T
A
27
GENIC
homozygous
61450181
1
82601688
82601689
C
T
21
GENIC
homozygous
61669586
1
82603490
82603491
C
T
14
INTERGENIC
homozygous
61669587
1
82603622
82603623
A
G
15
INTERGENIC
homozygous
61450184
1
82603711
82603712
G
A
25
INTERGENIC
possibly homozygous
61450185
1
82603761
82603762
G
A
25
INTERGENIC
possibly homozygous
61450186
1
82605589
82605590
G
A
27
INTERGENIC
homozygous
61450188
1
82606541
82606542
A
G
22
INTERGENIC
homozygous
61669588
1
82606830
82606831
T
G
34
INTERGENIC
possibly homozygous
61669589
1
82607048
82607049
G
A
28
INTERGENIC
possibly homozygous
61669590
1
82607257
82607258
C
CA
4
INTERGENIC
heterozygous
62137454
1
82607257
82607258
C
CAAA
4
INTERGENIC
heterozygous
62137455
1
82607995
82607996
C
T
28
INTERGENIC
homozygous
61669591
1
82608361
82608362
G
A
25
INTERGENIC
homozygous
61669592
