chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
4
61590764
61590765
G
A
16
GENIC
homozygous
56916623
4
61590786
61590787
T
C
14
GENIC
homozygous
56916624
4
61591132
61591133
A
C
30
GENIC
homozygous
56916625
4
61592142
61592143
G
A
26
GENIC
homozygous
56916626
4
61592379
61592380
A
G
20
GENIC
homozygous
56916627
4
61593235
61593236
A
-
17
GENIC
possibly homozygous
58587638
4
61593432
61593433
T
-
15
GENIC
possibly homozygous
57733192
4
61594397
61594457
GCAGGAGCCATTCCTCCTATCCAAGGACTAAGCACACCAGCATCCCTGTATCCTCTTAGA
------------------------------------------------------------
7
GENIC
homozygous
58336523
4
61595000
61595001
C
T
39
GENIC
homozygous
56916631
4
61595087
61595088
T
-
38
GENIC
homozygous
56916632
4
61595689
61595690
C
G
34
GENIC
homozygous
56916633
4
61596463
61596464
C
T
34
GENIC
homozygous
56916634
4
61597393
61597394
G
A
27
GENIC
possibly homozygous
56916635
4
61597727
61597728
T
-
9
GENIC
homozygous
56916636
4
61597731
61597738
TGTTGTG
-------
9
GENIC
homozygous
56916637
4
61598583
61598584
C
A
22
GENIC
homozygous
56916639
4
61598835
61598836
C
A
20
GENIC
homozygous
56916640
4
61599872
61599873
T
C
21
GENIC
homozygous
56916641
