chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
10572093
10572094
T
C
13
GENIC
homozygous
46059312
19
10572350
10572351
C
T
22
GENIC
homozygous
46059313
19
10573115
10573116
C
A
23
GENIC
homozygous
46059314
19
10573297
10573298
G
C
15
GENIC
homozygous
46059315
19
10573355
10573356
T
A
21
GENIC
homozygous
46059316
19
10573410
10573411
C
G
15
GENIC
homozygous
46059317
19
10573899
10573900
A
-
18
GENIC
homozygous
46059318
19
10574087
10574088
T
C
22
GENIC
homozygous
46059319
19
10574287
10574288
G
T
17
GENIC
homozygous
46059320
19
10575019
10575020
G
A
16
GENIC
homozygous
46059321
19
10575181
10575182
T
TA
8
GENIC
homozygous
46059322
19
10575567
10575590
CTCCCTCCCTCCCTCCCTCCCTC
-----------------------
7
GENIC
possibly homozygous
46059324
19
10575563
10575564
C
-
7
GENIC
heterozygous
46507213
19
10575565
10575590
CTCTCCCTCCCTCCCTCCCTCCCTC
-------------------------
7
GENIC
heterozygous
46458601
19
10575565
10575566
C
-
7
GENIC
possibly homozygous
46458603
19
10575789
10575790
C
A
18
GENIC
homozygous
46059325
19
10576099
10576101
GC
--
3
GENIC
heterozygous
46428079
19
10576100
10576101
C
CAAAAAAAAAA
3
GENIC
heterozygous
46428082
19
10576360
10576361
C
G
3
GENIC
homozygous
46059328
