chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
104195752
104195753
C
A
16
GENIC
homozygous
108735625
1
104195755
104195761
CCCCCC
17
GENIC
homozygous
127409404
1
104198136
104198137
C
4
GENIC
homozygous
127409405
1
104198067
104198114
ACACACACATTCACACACAACCATAATACACACCCATACACGCAATG
1
GENIC
homozygous
130519497
1
104198705
104198706
C
A
25
GENIC
homozygous
108165709
1
104198716
104198718
CT
27
GENIC
homozygous
127409410
1
104198732
104198733
A
31
GENIC
homozygous
127409411
1
104198849
104198850
G
41
GENIC
homozygous
127409412
1
104200493
104200493
AAATTCATCTCCAGATAAGT
52
GENIC
possibly homozygous
127409413
1
104200497
104200497
CTGCAGAGGAAAAGGTAAACAGT
44
GENIC
homozygous
127409414
1
104200500
104200500
TCG
29
GENIC
homozygous
127409415
1
104200503
104200503
TGAAACAAA
25
GENIC
homozygous
127409416
1
104200506
104200506
TGACAGATTTACCGGGGGGCATC
24
GENIC
homozygous
127409417
1
104200512
104200512
AGATGACTAAC
15
GENIC
homozygous
127409418
1
104200516
104200516
CTTACCCACACGTACACACGGTTTGAACAGC
9
GENIC
homozygous
127409419
1
104200519
104200519
AACAAA
17
GENIC
homozygous
127409420
1
104201321
104201322
C
G
63
GENIC
homozygous
108165710
1
104201340
104201341
C
A
65
GENIC
homozygous
108165711
1
104200510
104200511
G
C
15
GENIC
homozygous
127546319
