chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
36763448
36763449
G
GGGCTGTGTAGAGACCCTGTCTCAAAAACAAACAACCAACAAACCCCCAAACCAACCAACCAACAGCCAACCCCAACTCCATCCATCTGTC
23
GENIC
homozygous
46461330
19
36766882
36766883
C
T
33
GENIC
homozygous
46109418
19
36767132
36767133
C
T
38
GENIC
homozygous
46109420
19
36767582
36767583
A
G
10
GENIC
homozygous
46109422
19
36767752
36767754
TT
--
15
GENIC
possibly homozygous
46109424
19
36767753
36767754
T
-
15
GENIC
heterozygous
46109426
19
36768471
36768472
C
CT
10
GENIC
homozygous
46109428
19
36769408
36769409
G
GA
11
GENIC
heterozygous
46109432
19
36769483
36769484
G
GA
21
GENIC
homozygous
46109434
19
36769503
36769504
A
AG
19
GENIC
homozygous
46109436
19
36769541
36769542
A
C
11
GENIC
homozygous
46380049
19
36768636
36768637
C
CACACACACACACACACACACAT
10
GENIC
homozygous
46380045
19
36769540
36769541
C
A
11
GENIC
homozygous
46380047
19
36769553
36769554
A
G
12
GENIC
homozygous
46109438
19
36769583
36769584
C
-
15
GENIC
homozygous
46109440
19
36769611
36769612
T
A
19
GENIC
homozygous
46109442
19
36769615
36769616
G
GC
19
GENIC
homozygous
46109444
19
36772540
36772541
C
CTA
22
GENIC
homozygous
46109445
19
36775220
36775221
T
TCACACACACACA
11
GENIC
heterozygous
46461332
19
36775220
36775221
T
TCACACACACACACA
11
GENIC
possibly homozygous
46461334
19
36776224
36776225
T
TCA
7
GENIC
homozygous
46109449
19
36773746
36773747
A
-
14
GENIC
heterozygous
46429696
