chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
13024128
13024129
C
A
28
GENIC
homozygous
53792468
7
13024976
13024977
A
-
8
GENIC
homozygous
54301910
7
13024993
13024994
C
CAAA
17
GENIC
homozygous
53792470
7
13026281
13026287
CACACA
------
15
GENIC
homozygous
56142749
7
13026620
13026621
G
A
37
GENIC
homozygous
56142752
7
13026707
13026708
C
T
42
GENIC
homozygous
56142754
7
13027520
13027521
G
GAAAA
17
GENIC
heterozygous
54301913
7
13027520
13027521
G
GAAA
17
GENIC
possibly homozygous
55057510
7
13030385
13030386
A
T
37
GENIC
homozygous
56142757
7
13031444
13031445
A
-
8
GENIC
heterozygous
56142760
7
13032324
13032325
C
T
30
GENIC
homozygous
56142763
7
13033232
13033233
T
C
19
GENIC
homozygous
53792478
7
13033481
13033482
T
C
31
GENIC
homozygous
53792479
7
13033933
13033934
G
A
19
GENIC
homozygous
56142766
7
13035704
13035705
C
CTTGGAGCAGT
48
GENIC
homozygous
53792480
7
13036346
13036347
C
G
32
GENIC
homozygous
53792482
7
13037149
13037150
A
G
15
GENIC
homozygous
53792484
7
13037169
13037170
G
GC
8
GENIC
homozygous
55126565
7
13037372
13037373
A
G
20
GENIC
homozygous
53792485
7
13039190
13039191
T
C
34
GENIC
homozygous
53792487
7
13041287
13041288
A
AC
15
GENIC
homozygous
53792489
7
13042528
13042529
A
ACCT
38
GENIC
homozygous
53792492
7
13042688
13042689
T
C
34
GENIC
homozygous
56142769
7
13042822
13042823
C
T
14
GENIC
possibly homozygous
56142772
7
13042856
13042857
T
C
14
GENIC
possibly homozygous
53792493
7
13043051
13043052
C
A
23
GENIC
homozygous
53792494
7
13043421
13043422
C
T
31
GENIC
possibly homozygous
53792495
7
13043696
13043697
A
G
30
GENIC
homozygous
53792496
7
13048476
13048477
C
CTT
37
GENIC
homozygous
56142775
7
13049007
13049008
G
A
29
GENIC
homozygous
56142778
7
13050526
13050527
C
T
35
GENIC
homozygous
56142781
7
13050774
13050775
T
C
28
GENIC
possibly homozygous
53792499
7
13037697
13037698
A
ATGTGTGTGTGTGTGTGTGTGTGTGTG
5
GENIC
homozygous
55391595