chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
18
60853480
60853481
G
A
31
GENIC
homozygous
46689558
18
60854391
60854392
C
A
46
GENIC
homozygous
46689559
18
60854407
60854408
C
T
42
GENIC
homozygous
46689560
18
60855557
60855558
T
G
36
GENIC
homozygous
46480463
18
60856438
60856439
G
A
36
GENIC
homozygous
46689561
18
60858385
60858386
T
C
40
GENIC
homozygous
46480467
18
60858934
60858935
C
T
36
GENIC
homozygous
46689562
18
60859471
60859473
TA
--
14
GENIC
homozygous
46480482
18
60860133
60860134
G
A
34
GENIC
homozygous
46689563
18
60861233
60861234
G
A
17
GENIC
homozygous
46689564
18
60861305
60861306
G
A
26
GENIC
homozygous
46689565
18
60861569
60861570
T
-
17
GENIC
homozygous
46666192
18
60861717
60861718
C
T
17
GENIC
homozygous
46689566
18
60861784
60861785
G
A
19
GENIC
homozygous
46689567
18
60861813
60861814
G
A
23
GENIC
homozygous
46689568
18
60862065
60862066
T
C
27
GENIC
homozygous
46480492
18
60862597
60862598
G
GCA
37
GENIC
possibly homozygous
46689569
18
60862660
60862661
T
C
49
GENIC
homozygous
46666194
18
60864395
60864396
G
C
34
GENIC
homozygous
46689570
18
60865549
60865550
C
T
28
GENIC
homozygous
46689571
18
60865881
60865882
T
G
36
GENIC
homozygous
46480500
18
60865885
60865886
G
T
35
GENIC
homozygous
46480501
18
60865929
60865930
A
AGTCT
39
GENIC
homozygous
46480502
18
60866172
60866173
G
A
27
GENIC
homozygous
46480504
18
60867345
60867346
G
GTT
13
GENIC
heterozygous
46480508
18
60867715
60867716
T
C
17
GENIC
homozygous
46480509
18
60867345
60867346
G
GT
13
GENIC
heterozygous
46819154
18
60857425
60857426
T
TCTCTCTCTCTCTCTCTCTCTCTCTCC
12
GENIC
homozygous
46819153
