chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
14
61249719
61249720
G
C
22
GENIC
homozygous
48747793
14
61251344
61251345
A
G
38
GENIC
homozygous
48747795
14
61251880
61251881
C
T
25
GENIC
homozygous
48747797
14
61252066
61252067
G
-
15
GENIC
homozygous
48747799
14
61252074
61252075
G
-
15
GENIC
homozygous
48747801
14
61252077
61252078
C
-
15
GENIC
homozygous
48747803
14
61256939
61256940
A
G
16
GENIC
homozygous
48747805
14
61260725
61260726
A
C
18
GENIC
homozygous
49311072
14
61260727
61260728
T
A
20
GENIC
homozygous
49311073
14
61260738
61260739
C
-
22
GENIC
homozygous
48747807
14
61260742
61260743
C
T
24
GENIC
homozygous
49311074
14
61260745
61260746
T
-
24
GENIC
homozygous
48747809
14
61260749
61260750
C
G
27
GENIC
homozygous
48747811
14
61260755
61260756
A
T
29
GENIC
homozygous
48747813
14
61260758
61260759
C
G
27
GENIC
homozygous
48747815
14
61260764
61260765
A
-
29
GENIC
homozygous
48747817
14
61260768
61260769
C
-
30
GENIC
homozygous
48747818
14
61260774
61260775
A
-
32
GENIC
homozygous
48747820
14
61260781
61260782
G
-
33
GENIC
homozygous
48747822
14
61260783
61260784
A
T
35
GENIC
homozygous
49288793
14
61260810
61260811
T
TA
41
GENIC
homozygous
48747824
14
61260814
61260816
AA
--
43
GENIC
homozygous
48747826
14
61263292
61263293
C
T
9
GENIC
homozygous
48747828
14
61275911
61275912
C
T
26
GENIC
homozygous
48747829
14
61276438
61276439
T
C
28
GENIC
homozygous
48747831
14
61278402
61278403
A
-
24
GENIC
homozygous
48747833
14
61279230
61279231
A
-
11
GENIC
possibly homozygous
48747835
14
61279605
61279606
C
CCCTCTTGTCTTACAGATGTGGTTAGGT
46
GENIC
homozygous
48747839
14
61282872
61282873
A
-
18
GENIC
possibly homozygous
48747841
14
61284068
61284069
A
G
25
GENIC
homozygous
48747843
14
61285639
61285640
G
A
28
GENIC
homozygous
48747845
14
61286277
61286278
C
G
24
GENIC
homozygous
48747847
