chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
5859920
5859921
A
G
32
GENIC
homozygous
51798967
10
5860588
5860589
T
C
23
GENIC
homozygous
51611044
10
5860943
5860944
A
AGT
34
GENIC
possibly homozygous
51798970
10
5862036
5862037
G
GA
12
GENIC
possibly homozygous
51312362
10
5862207
5862208
T
C
27
GENIC
homozygous
51611045
10
5862263
5862264
T
C
29
GENIC
homozygous
51798972
10
5862301
5862302
A
G
23
GENIC
possibly homozygous
51611046
10
5862501
5862502
G
A
39
GENIC
homozygous
51798975
10
5864418
5864419
A
G
20
GENIC
homozygous
51798977
10
5865143
5865144
C
CTCAT
24
GENIC
homozygous
51312365
10
5865679
5865680
A
G
33
GENIC
homozygous
51611049
10
5866194
5866195
G
A
28
GENIC
homozygous
51798980
10
5866269
5866270
G
A
17
GENIC
homozygous
51798982
10
5866416
5866417
C
T
22
GENIC
homozygous
51312367
10
5866791
5866792
G
GTA
31
GENIC
homozygous
51798984
10
5866982
5866983
A
G
38
GENIC
homozygous
51312369
10
5868386
5868392
AAAAAA
------
7
GENIC
possibly homozygous
51798986
10
5869310
5869311
C
-
46
GENIC
homozygous
51798988
10
5869746
5869747
T
C
39
GENIC
homozygous
51611052
10
5869848
5869849
C
T
27
GENIC
homozygous
51798991
10
5871464
5871465
C
A
28
GENIC
homozygous
51798994
10
5872426
5872427
T
G
38
GENIC
homozygous
51312372
10
5872698
5872699
G
A
39
GENIC
homozygous
51798996
10
5873050
5873051
A
T
12
GENIC
homozygous
51798998
10
5873570
5873571
T
C
25
GENIC
homozygous
51611054
10
5876277
5876278
C
A
21
GENIC
homozygous
51312374
10
5876278
5876279
C
A
21
GENIC
homozygous
51312375
10
5876281
5876282
C
G
21
GENIC
homozygous
51312377
10
5876282
5876283
C
A
20
GENIC
homozygous
51312379
10
5876286
5876287
C
G
20
GENIC
homozygous
51312380
10
5877681
5877682
A
G
27
GENIC
homozygous
51611055
10
5877815
5877826
GTGTGTGTGTG
-----------
22
GENIC
possibly homozygous
51611057
10
5878618
5878619
C
CCTTACGGCGGTCTGGGGCAGCAAG
9
GENIC
homozygous
51312382
10
5877955
5877956
G
-
23
GENIC
homozygous
52294959
