chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
30118601
30118602
C
A
49
GENIC
homozygous
138049856
7
30118709
30118710
T
C
52
GENIC
homozygous
138049857
7
30118727
30118747
GTGTGGCCTTGTTGGAGTAG
45
GENIC
homozygous
137944763
7
30119180
30119181
A
G
36
GENIC
homozygous
138049860
7
30120114
30120115
C
G
43
GENIC
homozygous
138049861
7
30120483
30120484
T
C
25
GENIC
homozygous
138049863
7
30121084
30121085
T
C
35
GENIC
homozygous
138049864
7
30121144
30121145
G
A
31
GENIC
homozygous
138049865
7
30121456
30121457
A
C
47
GENIC
possibly homozygous
138049866
7
30121904
30121905
T
C
43
GENIC
homozygous
138049867
7
30122280
30122280
AA
40
GENIC
homozygous
137944764
7
30122578
30122579
T
C
55
GENIC
homozygous
138049868
7
30122636
30122637
G
A
53
GENIC
homozygous
138049869
7
30122964
30122965
T
G
48
GENIC
homozygous
138049870
7
30123012
30123013
C
T
40
GENIC
homozygous
144786920
7
30119791
30119792
G
A
48
GENIC
homozygous
144786918
7
30120304
30120305
A
G
54
GENIC
homozygous
144786919
7
30123120
30123121
A
T
51
GENIC
homozygous
138049871
7
30123187
30123188
G
50
GENIC
homozygous
137944765
7
30123217
30123218
G
A
44
GENIC
homozygous
138049872
7
30124555
30124556
T
A
51
GENIC
homozygous
138049874
7
30124771
30124771
CA
56
GENIC
homozygous
137944767
7
30124874
30124875
C
T
50
GENIC
homozygous
138049875
7
30126335
30126336
T
C
39
GENIC
homozygous
138049876
7
30126788
30126789
T
G
28
GENIC
homozygous
138049879
7
30127799
30127800
G
A
46
GENIC
homozygous
144786921
7
30120498
30120499
C
A
29
GENIC
homozygous
403206265
7
30120498
30120499
C
29
GENIC
heterozygous
403206266
7
30127827
30127828
A
G
50
GENIC
homozygous
138049881
7
30128096
30128112
AGCAGCGACCACCCTC
44
GENIC
homozygous
137944770
7
30128229
30128230
T
C
21
GENIC
homozygous
141949344
7
30128261
30128262
C
G
4
GENIC
homozygous
144786922
7
30128946
30128947
T
11
GENIC
homozygous
403828610
7
30128259
30128260
T
C
5
GENIC
heterozygous
403206267
7
30128259
30128260
T
G
5
GENIC
heterozygous
403206268
7
30128259
30128260
T
5
GENIC
homozygous
144778737
7
30128946
30128975
TGCCTTACAGTGGGCACGTTACCAGAGCA
11
GENIC
homozygous
144778738
7
30128946
30128947
T
C
11
GENIC
heterozygous
403828611
7
30128977
30128978
G
C
11
GENIC
homozygous
144786923
7
30128977
30128978
G
11
GENIC
heterozygous
403828612
7
30129036
30129096
CTTACAGTGGGCACGTTACCAGAGCACTGCCTTACAGTGGGCAAGTTACCAGAGCACTGC
33
GENIC
possibly homozygous
144778739
7
30129079
30129080
A
C
33
GENIC
heterozygous
403206274
7
30129079
30129080
A
33
GENIC
possibly homozygous
403206275
7
30129089
30129090
G
33
GENIC
possibly homozygous
403206276
7
30129089
30129090
G
A
33
GENIC
heterozygous
403206277
7
30129093
30129094
T
33
GENIC
possibly homozygous
403206278
7
30129093
30129094
T
C
33
GENIC
heterozygous
403206279
7
30129095
30129096
C
33
GENIC
possibly homozygous
403206280
7
30129095
30129096
C
T
33
GENIC
heterozygous
403206281
7
30129959
30129960
A
G
46
GENIC
homozygous
141949348
7
30130648
30130649
T
G
56
GENIC
homozygous
144786924
7
30131025
30131026
A
T
39
GENIC
homozygous
144786925
7
30131100
30131101
C
T
52
GENIC
homozygous
144786926
7
30131610
30131611
C
T
36
GENIC
homozygous
144021276
7
30132114
30132115
C
T
47
GENIC
possibly homozygous
144786927
7
30133298
30133298
A
47
GENIC
homozygous
141909888
7
30134567
30134568
G
A
45
GENIC
homozygous
141949352
7
30135316
30135317
C
16
GENIC
possibly homozygous
403206282
7
30135316
30135317
C
A
16
GENIC
heterozygous
403206283
7
30135862
30135863
C
A
27
GENIC
homozygous
138049893
7
30137219
30137220
A
G
47
GENIC
homozygous
138049896
7
30138460
30138461
G
A
45
GENIC
homozygous
141949353
7
30138919
30138919
AGA
36
GENIC
homozygous
137944775
7
30139168
30139169
G
45
GENIC
homozygous
137944776
7
30139894
30139895
G
C
55
GENIC
homozygous
144786928
7
30140089
30140090
C
T
47
GENIC
homozygous
138049897
