chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
14
103451255
103451256
T
A
39
GENIC
homozygous
139612754
14
103453323
103453324
A
G
49
GENIC
homozygous
139612755
14
103463027
103463028
G
A
48
GENIC
homozygous
139612756
14
103464842
103464843
C
G
49
GENIC
homozygous
139612757
14
103464904
103464905
C
T
49
GENIC
homozygous
139612758
14
103471442
103471443
T
C
53
GENIC
homozygous
139612759
14
103471575
103471576
C
T
19
GENIC
homozygous
139612760
14
103472208
103472209
G
C
60
GENIC
homozygous
139612761
14
103472971
103472972
T
G
56
GENIC
possibly homozygous
139612762
14
103473021
103473022
C
A
45
GENIC
homozygous
139612763
14
103480016
103480017
A
T
33
GENIC
homozygous
139612764
14
103480314
103480315
A
G
43
GENIC
homozygous
139612765
14
103480591
103480592
C
A
45
GENIC
homozygous
139612766
14
103482584
103482585
A
T
63
GENIC
homozygous
139612767
14
103482716
103482717
C
T
45
GENIC
homozygous
139612768
14
103483251
103483252
T
C
52
GENIC
homozygous
139612769
14
103484148
103484148
T
36
GENIC
possibly homozygous
139414710
14
103458335
103458335
TATT
57
GENIC
homozygous
139414705
14
103466163
103466164
T
27
GENIC
heterozygous
139414706
14
103478019
103478019
AGAGTGATGGG
25
GENIC
possibly homozygous
139414708
14
103483552
103483675
CTTATTACTAGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC
15
GENIC
heterozygous
139414709
14
103486245
103486246
G
T
52
GENIC
homozygous
139612770
14
103486793
103486793
A
52
GENIC
homozygous
139414711
14
103486794
103486794
AAACA
53
GENIC
homozygous
139414712
14
103486796
103486797
T
A
50
GENIC
homozygous
139612771
14
103487264
103487265
G
A
27
GENIC
homozygous
139612772
14
103487506
103487507
A
G
48
GENIC
homozygous
139612773
14
103495955
103495956
T
C
54
GENIC
homozygous
139612774
14
103496135
103496161
TAGGTATGATGCTCACTCTTAGACGG
46
GENIC
homozygous
139414713