chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
90521372
90521373
G
GC
3
GENIC
homozygous
51538631
10
90521433
90521434
G
GT
4
GENIC
heterozygous
51538633
10
90521475
90521476
G
GC
5
GENIC
homozygous
51538634
10
90521495
90521496
T
TC
8
GENIC
homozygous
51538635
10
90522496
90522497
C
T
18
GENIC
homozygous
51736877
10
90522541
90522542
A
G
20
GENIC
homozygous
51736879
10
90522619
90522620
C
A
12
GENIC
homozygous
51736881
10
90523477
90523478
A
T
19
GENIC
homozygous
51736886
10
90523662
90523663
G
A
26
GENIC
homozygous
51736888
10
90523679
90523680
C
A
27
GENIC
homozygous
52165642
10
90523889
90523890
C
A
22
GENIC
homozygous
51736890
10
90524611
90524612
T
C
23
GENIC
homozygous
51736892
10
90524927
90524928
C
A
27
GENIC
homozygous
52165643
10
90525183
90525184
G
A
20
GENIC
homozygous
52165644
10
90525549
90525550
C
T
21
GENIC
homozygous
52165645
10
90526021
90526029
TGTGAGTG
--------
11
GENIC
possibly homozygous
52445659
10
90526023
90526029
TGAGTG
------
11
GENIC
heterozygous
52396547
10
90526087
90526088
G
GA
12
GENIC
homozygous
52396549
10
90526089
90526090
A
ACTCAGTTTGAGATCTGTGAGTGAGCTGAGCCTTCTGGGGACTGGCAGGGATTGGCTCTGCAGATGAGGCC
12
GENIC
homozygous
52396550
10
90526093
90526094
G
T
12
GENIC
homozygous
52396552
10
90529705
90529706
C
T
30
GENIC
homozygous
52206543
10
90529817
90529818
T
C
25
GENIC
homozygous
52165646
10
90530156
90530157
T
TG
26
GENIC
homozygous
52165647
10
90531806
90531807
T
C
17
GENIC
homozygous
51736905
10
90532766
90532767
T
C
19
GENIC
homozygous
51736909
10
90532827
90532828
T
G
15
GENIC
homozygous
51736911
10
90533671
90533672
A
G
11
GENIC
homozygous
52165648
10
90533861
90533862
C
T
27
GENIC
homozygous
52165649
10
90537525
90537526
A
T
17
GENIC
homozygous
52206546
