chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
4
135690359
135690360
C
T
9
GENIC
homozygous
56939037
4
135690889
135690890
G
A
3
GENIC
homozygous
56939038
4
135691660
135691661
T
A
18
GENIC
homozygous
56939040
4
135691722
135691723
G
A
22
GENIC
homozygous
56939041
4
135692567
135692568
G
T
26
GENIC
homozygous
56939042
4
135692820
135692823
CAG
---
22
GENIC
homozygous
58282885
4
135692823
135692824
A
AC
22
GENIC
homozygous
58282887
4
135694573
135694574
G
A
22
GENIC
homozygous
56939045
4
135694723
135694724
G
GT
20
GENIC
possibly homozygous
56939046
4
135694723
135694724
G
GTT
20
GENIC
heterozygous
58338647
4
135695018
135695019
G
C
41
GENIC
homozygous
56939047
4
135695676
135695677
A
G
26
GENIC
homozygous
56939048
4
135696770
135696771
T
C
26
GENIC
homozygous
56939049
4
135697479
135697480
C
T
31
GENIC
homozygous
56939050
4
135697528
135697529
T
C
31
GENIC
homozygous
56939051
4
135697955
135697956
C
T
33
GENIC
homozygous
56939052
4
135697974
135697975
C
T
27
GENIC
homozygous
56939053
4
135699720
135699721
A
G
14
GENIC
homozygous
56939054
4
135700489
135700490
G
A
28
GENIC
homozygous
56939055
4
135702788
135702789
G
GGGCTTCTAGGCGCATGCCTGGTGA
17
GENIC
homozygous
56939058
4
135703099
135703100
T
C
19
GENIC
homozygous
56939059
4
135703569
135703571
GT
--
6
GENIC
heterozygous
56939060
4
135704927
135704928
G
A
27
GENIC
homozygous
56939061
