chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
106338269
106338270
A
T
5
GENIC
homozygous
51590538
10
106339683
106339685
GT
--
5
GENIC
heterozygous
52463031
10
106351703
106351705
AC
--
15
GENIC
heterozygous
51765385
10
106354189
106354190
T
C
11
GENIC
homozygous
51590543
10
106362564
106362565
G
GTTT
16
GENIC
homozygous
51590545
10
106367663
106367664
T
TAC
3
GENIC
heterozygous
51590549
10
106368841
106368842
T
TG
4
GENIC
homozygous
51590551
10
106372366
106372369
TGC
---
1
GENIC
homozygous
52463032
10
106374268
106374269
C
-
6
GENIC
homozygous
51590559
10
106341213
106341214
A
ATG
2
GENIC
heterozygous
52514847
10
106347091
106347093
GT
--
6
GENIC
heterozygous
52447725
10
106384747
106384748
A
ATG
5
GENIC
homozygous
52407076
10
106384750
106384751
T
TGCTAGGCAAGCGCTCTACCACTGAGCTAAA
3
GENIC
homozygous
52407078
10
106384755
106384757
GG
--
4
GENIC
homozygous
52447731
10
106384758
106384759
G
-
5
GENIC
homozygous
51590577
10
106393629
106393630
T
-
22
GENIC
possibly homozygous
52447733
10
106402252
106402253
G
GA
13
GENIC
homozygous
51590581