chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
10668617
10668618
C
A
26
GENIC
homozygous
46059687
19
10669199
10669200
G
GGA
23
GENIC
homozygous
46059688
19
10669549
10669550
C
CAAGGCTGGAGACTGGG
30
GENIC
homozygous
46059689
19
10669705
10669706
T
C
30
GENIC
homozygous
46059690
19
10670072
10670073
A
G
23
GENIC
homozygous
46788895
19
10670228
10670229
T
TTCTGTGTGTGTG
3
GENIC
homozygous
46788897
19
10670600
10670601
T
G
38
GENIC
possibly homozygous
46059693
19
10670732
10670733
T
G
19
GENIC
homozygous
46059694
19
10670904
10670905
A
G
16
GENIC
homozygous
46059695
19
10671270
10671271
T
-
15
GENIC
homozygous
46059696
19
10671355
10671356
C
T
12
GENIC
homozygous
46546797
19
10672148
10672149
A
G
20
GENIC
possibly homozygous
46059699
19
10672556
10672560
GGAG
----
8
GENIC
possibly homozygous
46397446
19
10672561
10672613
GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGGAGGGAGGGAGG
----------------------------------------------------
10
GENIC
heterozygous
46397448
19
10673328
10673329
T
-
34
GENIC
homozygous
46788899
19
10673562
10673563
C
T
28
GENIC
homozygous
46059704
19
10674212
10674213
T
C
38
GENIC
homozygous
46059705
19
10674742
10674743
A
G
17
GENIC
homozygous
46059706
19
10674778
10674779
T
C
16
GENIC
homozygous
46059707
19
10674905
10674906
C
T
23
GENIC
homozygous
46486236
19
10672555
10672567
GGGAGAGAGAGA
------------
8
GENIC
heterozygous
46458634
19
10670504
10670505
C
CTTTTTTTT
2
GENIC
homozygous
46428089