chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
105207501
105207502
A
T
24
GENIC
homozygous
61491699
1
105207708
105207709
G
T
18
GENIC
possibly homozygous
62148289
1
105207710
105207711
G
T
19
GENIC
possibly homozygous
62148291
1
105207712
105207713
G
T
20
GENIC
possibly homozygous
62148293
1
105207713
105207714
G
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAT
27
GENIC
homozygous
62085483
1
105207883
105207884
T
C
36
GENIC
homozygous
61737353
1
105212116
105212117
C
T
19
GENIC
homozygous
61737355
1
105212880
105212884
GATA
----
4
GENIC
homozygous
62148297
1
105212957
105212958
A
G
17
GENIC
homozygous
61491720
1
105213674
105213675
C
T
24
GENIC
homozygous
61737357
1
105213758
105213759
G
A
30
GENIC
homozygous
61737359
1
105213915
105213916
T
G
25
GENIC
homozygous
61737361
1
105214154
105214155
A
-
10
GENIC
homozygous
61737363
1
105214252
105214253
A
G
16
GENIC
homozygous
61737365
1
105214335
105214336
G
A
18
GENIC
homozygous
61737367
1
105214416
105214417
C
T
20
GENIC
homozygous
61737369
1
105214436
105214437
T
G
19
GENIC
homozygous
61737371
1
105215229
105215230
G
A
23
GENIC
possibly homozygous
61737373
1
105219382
105219383
A
G
17
GENIC
homozygous
61737375
1
105219473
105219474
A
AGTGTGT
6
GENIC
heterozygous
61491734
1
105219473
105219474
A
AGTGT
6
GENIC
heterozygous
61491735
1
105221107
105221108
T
TGACA
20
GENIC
homozygous
61491736
1
105222120
105222121
C
CCTG
16
GENIC
homozygous
62085484
1
105222652
105222653
T
C
19
GENIC
homozygous
61491739
1
105222773
105222774
G
C
28
GENIC
homozygous
61737377
1
105224362
105224363
T
C
26
GENIC
homozygous
61737379
