chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
14
61249719
61249720
G
C
54
GENIC
possibly homozygous
48747793
14
61251344
61251345
A
G
29
GENIC
homozygous
48747795
14
61251880
61251881
C
T
32
GENIC
homozygous
48747797
14
61252066
61252067
G
-
35
GENIC
homozygous
48747799
14
61252074
61252075
G
-
35
GENIC
homozygous
48747801
14
61252077
61252078
C
-
34
GENIC
possibly homozygous
48747803
14
61256939
61256940
A
G
41
GENIC
possibly homozygous
48747805
14
61260738
61260739
C
-
14
GENIC
homozygous
48747807
14
61260745
61260746
T
-
14
GENIC
homozygous
48747809
14
61260749
61260750
C
G
18
GENIC
homozygous
48747811
14
61260755
61260756
A
T
19
GENIC
homozygous
48747813
14
61260758
61260759
C
G
20
GENIC
homozygous
48747815
14
61260764
61260765
A
-
18
GENIC
homozygous
48747817
14
61260768
61260769
C
-
18
GENIC
homozygous
48747818
14
61260774
61260775
A
-
17
GENIC
homozygous
48747820
14
61260781
61260782
G
-
14
GENIC
homozygous
48747822
14
61260782
61260783
G
T
18
GENIC
heterozygous
49006004
14
61260810
61260811
T
TA
23
GENIC
homozygous
48747824
14
61260814
61260816
AA
--
23
GENIC
homozygous
48747826
14
61263292
61263293
C
T
21
GENIC
homozygous
48747828
14
61275911
61275912
C
T
39
GENIC
homozygous
48747829
14
61276438
61276439
T
C
48
GENIC
homozygous
48747831
14
61278402
61278403
A
-
42
GENIC
homozygous
48747833
14
61279230
61279231
A
-
25
GENIC
homozygous
48747835
14
61279605
61279606
C
CCCTCTTGTCTTACAGATGTGGTTAGGT
26
GENIC
homozygous
48747839
14
61282872
61282873
A
-
32
GENIC
homozygous
48747841
14
61284068
61284069
A
G
47
GENIC
homozygous
48747843
14
61285639
61285640
G
A
45
GENIC
homozygous
48747845
14
61286277
61286278
C
G
25
GENIC
homozygous
48747847
14
61286313
61286314
C
-
2
GENIC
homozygous
48747849
