geneid | 23192 |
---|---|
ensemblid | ENSG00000168397.17 |
hgncid | 20790 |
symbol | ATG4B |
name | autophagy related 4B cysteine peptidase |
refseq_nuc | NM_013325.5 |
refseq_prot | NP_037457.3 |
ensembl_nuc | ENST00000404914.8 |
ensembl_prot | ENSP00000384259.3 |
mane_status | MANE Select |
chr | chr2 |
start | 241637693 |
end | 241673857 |
strand | + |
ver | v1.2 |
region | chr2:241637693-241673857 |
region5000 | chr2:241632693-241678857 |
regionname0 | ATG4B_chr2_241637693_241673857 |
regionname5000 | ATG4B_chr2_241632693_241678857 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 393 | 324 | 70 | 57 | 151 | 11 | 34 | 112 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0002 | 1/0 | 393 | 58 | 4 | 7 | 37 | 3 | 6 | 35 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003 | 0/0 | 393 | 25 | 13 | 1 | 7 | 2 | 2 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0004 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0005 | 0/0 | 393 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0006 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1182 | 223 | 58 | 45 | 86 | 6 | 27 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0002 | 0/0 | 1182 | 87 | 10 | 10 | 56 | 5 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0003 | 1/0 | 1182 | 58 | 4 | 7 | 37 | 3 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0004 | 0/0 | 1182 | 23 | 11 | 1 | 7 | 2 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0005 | 0/0 | 1182 | 5 | 0 | 0 | 5 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0006 | 0/0 | 1182 | 4 | 2 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0007 | 0/0 | 1182 | 4 | 0 | 0 | 4 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0008 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0009 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0010 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0011 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
c0012 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1615 | 89 | 11 | 37 | 28 | 4 | 9 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0002 | 0/0 | 1612 | 74 | 9 | 4 | 45 | 2 | 14 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0003 | 0/0 | 1618 | 49 | 9 | 7 | 25 | 2 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0004 | 0/0 | 1615 | 46 | 11 | 6 | 25 | 3 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0005 | 0/0 | 1618 | 37 | 0 | 3 | 32 | 2 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0006 | 0/0 | 1611 | 17 | 16 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0007 | 0/0 | 1615 | 12 | 1 | 1 | 7 | 2 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0008 | 0/0 | 1615 | 12 | 0 | 0 | 12 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0009 | 0/0 | 1611 | 8 | 0 | 0 | 8 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0010 | 0/0 | 1615 | 8 | 8 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0011 | 0/1 | 1615 | 5 | 3 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0012 | 1/0 | 1616 | 5 | 1 | 0 | 0 | 0 | 3 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0013 | 0/0 | 1618 | 4 | 0 | 0 | 4 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0014 | 0/0 | 1615 | 4 | 2 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0015 | 0/0 | 1618 | 3 | 1 | 1 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0016 | 0/0 | 1614 | 3 | 1 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0017 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0018 | 0/0 | 1611 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0019 | 0/0 | 1615 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0020 | 0/0 | 1613 | 2 | 0 | 0 | 1 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0021 | 0/0 | 1612 | 2 | 0 | 0 | 0 | 0 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0022 | 0/0 | 1618 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0023 | 0/0 | 1618 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0024 | 0/0 | 1615 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0025 | 0/0 | 1618 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0026 | 0/0 | 1615 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0027 | 0/0 | 1615 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0028 | 0/0 | 1615 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0029 | 0/0 | 1618 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0030 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0031 | 0/0 | 1615 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0032 | 0/0 | 1616 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0033 | 0/0 | 1616 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0034 | 0/0 | 1615 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0035 | 0/0 | 1618 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0036 | 0/0 | 1612 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0037 | 0/0 | 1612 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0038 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0039 | 0/0 | 1612 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0040 | 0/0 | 1612 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0041 | 0/0 | 1615 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0042 | 0/0 | 1615 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0043 | 0/0 | 1616 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
t0044 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0002 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0013 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0034 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0318 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1182 | 223 | 58 | 45 | 86 | 6 | 27 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002 | 0/0 | 1182 | 87 | 10 | 10 | 56 | 5 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0005 | 0/0 | 1182 | 5 | 0 | 0 | 5 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0006 | 0/0 | 1182 | 4 | 2 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0007 | 0/0 | 1182 | 4 | 0 | 0 | 4 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0010 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0002c0003 | 1/0 | 1182 | 58 | 4 | 7 | 37 | 3 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003c0004 | 0/0 | 1182 | 23 | 11 | 1 | 7 | 2 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003c0008 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0004c0012 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0005c0009 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0006c0011 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2796 | 88 | 11 | 36 | 28 | 4 | 9 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0002 | 0/0 | 2793 | 73 | 9 | 4 | 45 | 2 | 13 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0004 | 0/0 | 2796 | 11 | 9 | 1 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0006 | 0/0 | 2792 | 17 | 16 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0009 | 0/0 | 2792 | 8 | 0 | 0 | 8 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0011 | 0/1 | 2796 | 5 | 3 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0012 | 0/0 | 2797 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0016 | 0/0 | 2795 | 3 | 1 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0017 | 0/0 | 2795 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0018 | 0/0 | 2792 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0020 | 0/0 | 2794 | 2 | 0 | 0 | 1 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0021 | 0/0 | 2793 | 2 | 0 | 0 | 0 | 0 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0028 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0031 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0032 | 0/0 | 2797 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0033 | 0/0 | 2797 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0036 | 0/0 | 2793 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0037 | 0/0 | 2793 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0038 | 0/0 | 2795 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0039 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0001t0040 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0003 | 0/0 | 2799 | 45 | 7 | 5 | 25 | 2 | 6 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0005 | 0/0 | 2799 | 28 | 0 | 3 | 23 | 2 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0013 | 0/0 | 2799 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0015 | 0/0 | 2799 | 3 | 1 | 1 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0022 | 0/0 | 2799 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0023 | 0/0 | 2799 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0025 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0029 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0030 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0035 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0002t0044 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0005t0005 | 0/0 | 2799 | 5 | 0 | 0 | 5 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0006t0003 | 0/0 | 2799 | 4 | 2 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0007t0005 | 0/0 | 2799 | 4 | 0 | 0 | 4 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0001c0010t0002 | 0/0 | 2793 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0002c0003t0004 | 0/0 | 2796 | 35 | 2 | 5 | 24 | 3 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0002c0003t0008 | 0/0 | 2796 | 12 | 0 | 0 | 12 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0002c0003t0012 | 1/0 | 2797 | 4 | 0 | 0 | 0 | 0 | 3 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0002c0003t0014 | 0/0 | 2796 | 4 | 2 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0002c0003t0041 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0002c0003t0042 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0002c0003t0043 | 0/0 | 2797 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003c0004t0007 | 0/0 | 2796 | 11 | 0 | 1 | 7 | 2 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003c0004t0010 | 0/0 | 2796 | 8 | 8 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003c0004t0024 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003c0004t0026 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003c0004t0027 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003c0004t0034 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0003c0008t0019 | 0/0 | 2796 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0004c0012t0013 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0005c0009t0001 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
a0006c0011t0007 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | copy fasta | chr2 | 241632693 | 241678857 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0013 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0034 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0006g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0009g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0009g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0011g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0011g0318 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0011g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0012g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0016g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0016g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0016g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0017g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0018g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0020g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0021g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0021g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0031g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0032g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0033g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0036g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0037g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0038g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0039g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0001t0040g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0013g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0013g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0015g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0015g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0022g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0022g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0023g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0025g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0029g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0030g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0035g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0002t0044g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0005t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0006t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0006t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0006t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0006t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0007t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0007t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0007t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0007t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0001c0010t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0012g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0012g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0014g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0014g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0014g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0014g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0041g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0042g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0002c0003t0043g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0010g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0024g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0026g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0027g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0004t0034g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0008t0019g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0003c0008t0019g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0004c0012t0013g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0005c0009t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
a0006c0011t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0092 | EUR | GBR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00140 | hp1 | a0002 | c0003 | t0004 | g0113 | EUR | GBR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00140 | hp2 | a0002 | c0003 | t0004 | g0132 | EUR | GBR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00280 | hp2 | a0001 | c0002 | t0005 | g0072 | EUR | FIN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00323 | hp1 | a0001 | c0002 | t0003 | g0095 | EUR | FIN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00323 | hp2 | a0001 | c0002 | t0005 | g0071 | EUR | FIN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00408 | hp2 | a0001 | c0002 | t0003 | g0043 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00438 | hp1 | a0001 | c0002 | t0022 | g0087 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00438 | hp2 | a0001 | c0001 | t0037 | g0293 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00544 | hp1 | a0001 | c0001 | t0032 | g0330 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00544 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00597 | hp1 | a0001 | c0002 | t0013 | g0079 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0098 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0127 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00609 | hp2 | a0001 | c0002 | t0003 | g0137 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00621 | hp1 | a0001 | c0002 | t0025 | g0187 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00621 | hp2 | a0001 | c0002 | t0013 | g0089 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0091 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00642 | hp1 | a0001 | c0001 | t0011 | g0036 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00673 | hp1 | a0001 | c0002 | t0005 | g0088 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | CHS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00735 | hp1 | a0002 | c0003 | t0004 | g0006 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00741 | hp1 | a0002 | c0003 | t0014 | g0351 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01071 | hp1 | a0002 | c0003 | t0014 | g0352 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01099 | hp1 | a0003 | c0004 | t0007 | g0209 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01106 | hp1 | a0001 | c0002 | t0023 | g0128 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01109 | hp1 | a0001 | c0006 | t0003 | g0123 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01167 | hp1 | a0002 | c0003 | t0004 | g0006 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01167 | hp2 | a0001 | c0001 | t0016 | g0159 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01168 | hp2 | a0001 | c0002 | t0003 | g0021 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01169 | hp1 | a0001 | c0001 | t0016 | g0161 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01169 | hp2 | a0001 | c0002 | t0003 | g0021 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01255 | hp2 | a0005 | c0009 | t0001 | g0101 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0147 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0148 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01496 | hp1 | a0001 | c0002 | t0015 | g0020 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01496 | hp2 | a0001 | c0006 | t0003 | g0204 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01515 | hp1 | a0003 | c0004 | t0007 | g0195 | EUR | IBS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | IBS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01517 | hp1 | a0002 | c0003 | t0004 | g0116 | EUR | IBS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01884 | hp2 | a0002 | c0003 | t0014 | g0202 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0341 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01928 | hp2 | a0002 | c0003 | t0004 | g0030 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0188 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01952 | hp1 | a0002 | c0003 | t0004 | g0030 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01952 | hp2 | a0001 | c0002 | t0005 | g0064 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01981 | hp1 | a0001 | c0002 | t0005 | g0063 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02027 | hp1 | a0001 | c0002 | t0005 | g0075 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02027 | hp2 | a0002 | c0003 | t0004 | g0022 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0348 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0094 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02056 | hp2 | a0003 | c0004 | t0007 | g0026 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02074 | hp2 | a0001 | c0007 | t0005 | g0065 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02080 | hp1 | a0001 | c0005 | t0005 | g0174 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02129 | hp2 | a0001 | c0002 | t0005 | g0085 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02132 | hp2 | a0001 | c0002 | t0005 | g0078 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02135 | hp1 | a0001 | c0002 | t0013 | g0068 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | KHV | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CDX | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02155 | hp2 | a0002 | c0003 | t0004 | g0083 | EAS | CDX | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | CDX | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | CDX | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02257 | hp1 | a0001 | c0002 | t0003 | g0162 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02258 | hp2 | a0001 | c0002 | t0003 | g0171 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02293 | hp2 | a0001 | c0002 | t0005 | g0062 | AMR | PEL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0164 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02572 | hp1 | a0002 | c0003 | t0014 | g0353 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0328 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0097 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02615 | hp1 | a0001 | c0006 | t0003 | g0134 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02622 | hp1 | a0003 | c0004 | t0010 | g0027 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0115 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02647 | hp1 | a0003 | c0004 | t0010 | g0205 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02683 | hp2 | a0001 | c0001 | t0036 | g0012 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0336 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02738 | hp2 | a0002 | c0003 | t0004 | g0138 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02809 | hp2 | a0002 | c0003 | t0004 | g0140 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02886 | hp1 | a0003 | c0004 | t0010 | g0206 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0343 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02965 | hp1 | a0001 | c0002 | t0044 | g0212 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0345 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02970 | hp1 | a0003 | c0004 | t0026 | g0028 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0036 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03017 | hp1 | a0001 | c0010 | t0002 | g0306 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03017 | hp2 | a0002 | c0003 | t0012 | g0009 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03041 | hp1 | a0003 | c0004 | t0024 | g0189 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03041 | hp2 | a0001 | c0006 | t0003 | g0122 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03098 | hp1 | a0003 | c0004 | t0010 | g0028 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03098 | hp2 | a0001 | c0001 | t0012 | g0155 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0245 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03209 | hp1 | a0003 | c0008 | t0019 | g0042 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0248 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03453 | hp1 | a0001 | c0001 | t0018 | g0015 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03453 | hp2 | a0001 | c0001 | t0017 | g0038 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03490 | hp2 | a0001 | c0001 | t0021 | g0252 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03491 | hp1 | a0003 | c0004 | t0027 | g0246 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03492 | hp1 | a0001 | c0001 | t0021 | g0002 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03516 | hp1 | a0001 | c0001 | t0033 | g0335 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ESN | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03540 | hp2 | a0001 | c0001 | t0040 | g0268 | AFR | GWD | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03579 | hp1 | a0003 | c0004 | t0010 | g0027 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03654 | hp2 | a0002 | c0003 | t0012 | g0009 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03669 | hp2 | a0001 | c0002 | t0003 | g0039 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03704 | hp1 | a0001 | c0002 | t0003 | g0074 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03710 | hp2 | a0002 | c0003 | t0041 | g0139 | SAS | PJL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03831 | hp2 | a0002 | c0003 | t0042 | g0142 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0099 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03927 | hp1 | a0001 | c0001 | t0020 | g0002 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03942 | hp1 | a0001 | c0002 | t0003 | g0019 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03942 | hp2 | a0003 | c0004 | t0007 | g0191 | SAS | BEB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04204 | hp1 | a0002 | c0003 | t0012 | g0009 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG04204 | hp2 | a0001 | c0001 | t0031 | g0037 | SAS | STU | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18522 | hp1 | a0001 | c0002 | t0003 | g0163 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0346 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | CHB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | CHB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18906 | hp1 | a0003 | c0008 | t0019 | g0041 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18906 | hp2 | a0001 | c0001 | t0038 | g0158 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18939 | hp1 | a0001 | c0005 | t0005 | g0199 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18941 | hp1 | a0003 | c0004 | t0007 | g0190 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18941 | hp2 | a0001 | c0002 | t0005 | g0076 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18942 | hp1 | a0001 | c0002 | t0005 | g0167 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18943 | hp1 | a0002 | c0003 | t0004 | g0119 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18944 | hp2 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18945 | hp2 | a0001 | c0002 | t0005 | g0124 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18946 | hp1 | a0001 | c0007 | t0005 | g0059 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18946 | hp2 | a0002 | c0003 | t0008 | g0052 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18947 | hp1 | a0002 | c0003 | t0004 | g0120 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18949 | hp1 | a0001 | c0002 | t0005 | g0073 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18949 | hp2 | a0002 | c0003 | t0008 | g0005 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18951 | hp1 | a0001 | c0002 | t0035 | g0016 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0105 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18953 | hp2 | a0001 | c0002 | t0005 | g0169 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18954 | hp1 | a0001 | c0005 | t0005 | g0203 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18954 | hp2 | a0002 | c0003 | t0004 | g0112 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18957 | hp1 | a0002 | c0003 | t0008 | g0049 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18957 | hp2 | a0001 | c0002 | t0005 | g0017 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18959 | hp1 | a0003 | c0004 | t0007 | g0194 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18959 | hp2 | a0001 | c0002 | t0003 | g0069 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18960 | hp1 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18961 | hp1 | a0002 | c0003 | t0008 | g0048 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18962 | hp1 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18963 | hp2 | a0002 | c0003 | t0004 | g0111 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18964 | hp1 | a0002 | c0003 | t0008 | g0005 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18965 | hp1 | a0001 | c0002 | t0005 | g0060 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18965 | hp2 | a0002 | c0003 | t0008 | g0045 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18966 | hp1 | a0003 | c0004 | t0007 | g0196 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18969 | hp1 | a0002 | c0003 | t0004 | g0081 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0126 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18971 | hp1 | a0001 | c0007 | t0005 | g0058 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18971 | hp2 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18972 | hp1 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18973 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18975 | hp1 | a0001 | c0002 | t0005 | g0077 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18975 | hp2 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18977 | hp1 | a0003 | c0004 | t0007 | g0207 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18977 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18978 | hp1 | a0002 | c0003 | t0008 | g0047 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18979 | hp1 | a0002 | c0003 | t0004 | g0175 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18981 | hp2 | a0002 | c0003 | t0004 | g0022 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18982 | hp1 | a0001 | c0002 | t0005 | g0084 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18984 | hp1 | a0002 | c0003 | t0004 | g0106 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18984 | hp2 | a0001 | c0002 | t0005 | g0066 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18985 | hp2 | a0002 | c0003 | t0004 | g0117 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18987 | hp1 | a0002 | c0003 | t0004 | g0240 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18987 | hp2 | a0002 | c0003 | t0004 | g0104 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18989 | hp1 | a0003 | c0004 | t0007 | g0200 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18990 | hp1 | a0002 | c0003 | t0008 | g0051 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18990 | hp2 | a0001 | c0001 | t0028 | g0001 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18991 | hp2 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18992 | hp1 | a0002 | c0003 | t0004 | g0133 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18993 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18994 | hp2 | a0001 | c0001 | t0020 | g0310 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18999 | hp1 | a0002 | c0003 | t0008 | g0005 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18999 | hp2 | a0001 | c0002 | t0005 | g0168 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19000 | hp2 | a0001 | c0002 | t0005 | g0170 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19005 | hp1 | a0002 | c0003 | t0004 | g0108 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19005 | hp2 | a0001 | c0002 | t0003 | g0102 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19006 | hp2 | a0004 | c0012 | t0013 | g0070 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19007 | hp2 | a0001 | c0005 | t0005 | g0198 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19009 | hp1 | a0003 | c0004 | t0007 | g0026 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19011 | hp2 | a0002 | c0003 | t0004 | g0118 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19012 | hp1 | a0002 | c0003 | t0004 | g0130 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19030 | hp1 | a0003 | c0004 | t0010 | g0192 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19030 | hp2 | a0001 | c0001 | t0011 | g0157 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19043 | hp1 | a0001 | c0001 | t0039 | g0281 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19043 | hp2 | a0001 | c0002 | t0030 | g0332 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19054 | hp1 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19055 | hp1 | a0002 | c0003 | t0004 | g0096 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19056 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19056 | hp2 | a0001 | c0002 | t0005 | g0080 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19060 | hp2 | a0001 | c0002 | t0005 | g0016 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19064 | hp1 | a0001 | c0002 | t0022 | g0086 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19066 | hp1 | a0001 | c0002 | t0005 | g0061 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19066 | hp2 | a0002 | c0003 | t0004 | g0109 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19067 | hp1 | a0001 | c0001 | t0009 | g0176 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19068 | hp1 | a0002 | c0003 | t0004 | g0082 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19068 | hp2 | a0001 | c0007 | t0005 | g0067 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19074 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19075 | hp1 | a0002 | c0003 | t0043 | g0121 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19076 | hp2 | a0002 | c0003 | t0008 | g0046 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19077 | hp1 | a0002 | c0003 | t0008 | g0050 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19080 | hp1 | a0001 | c0001 | t0009 | g0177 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19080 | hp2 | a0002 | c0003 | t0004 | g0280 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19081 | hp1 | a0002 | c0003 | t0008 | g0044 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19081 | hp2 | a0002 | c0003 | t0004 | g0271 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19083 | hp1 | a0001 | c0001 | t0009 | g0179 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19083 | hp2 | a0001 | c0002 | t0005 | g0166 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19084 | hp2 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19086 | hp1 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19087 | hp2 | a0001 | c0002 | t0005 | g0017 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19088 | hp2 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19090 | hp1 | a0001 | c0002 | t0029 | g0181 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19091 | hp1 | a0002 | c0003 | t0004 | g0131 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0344 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ASW | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20129 | hp2 | a0002 | c0003 | t0004 | g0165 | AFR | ASW | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20752 | hp1 | a0001 | c0002 | t0003 | g0223 | EUR | TSI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20752 | hp2 | a0003 | c0004 | t0007 | g0193 | EUR | TSI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0323 | EUR | TSI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20805 | hp2 | a0001 | c0002 | t0015 | g0020 | EUR | TSI | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20905 | hp1 | a0001 | c0002 | t0003 | g0019 | SAS | GIH | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0303 | SAS | GIH | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01123 | hp1 | a0002 | c0003 | t0004 | g0006 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02486 | hp2 | a0001 | c0001 | t0016 | g0160 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG02559 | hp2 | a0003 | c0004 | t0010 | g0201 | AFR | ACB | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03471 | hp1 | a0001 | c0001 | t0017 | g0038 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG03471 | hp2 | a0001 | c0001 | t0018 | g0015 | AFR | MSL | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG06807 | hp1 | a0003 | c0004 | t0010 | g0197 | AFR | USA | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0347 | AFR | USA | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18955 | hp1 | a0002 | c0003 | t0004 | g0107 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA18955 | hp2 | a0001 | c0005 | t0005 | g0180 | EAS | JPT | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA20300 | hp2 | a0003 | c0004 | t0034 | g0208 | AFR | USA | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA21309 | hp1 | a0006 | c0011 | t0007 | g0320 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
NA21309 | hp2 | a0001 | c0002 | t0015 | g0103 | AFR | LWK | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0011 | g0318 | REF | REF | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
homoSapiens_grch38 | hp1 | a0002 | c0003 | t0012 | g0214 | REF | REF | ATG4B_chr2_241632693_241678857 | ATG4B | chr2 | 241632693 | 241678857 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241651022
|
A | G | 1 | a0004 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.23A>G | p.Tyr8Cys | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 2/13 | 45/2797 | 23/1182 | 8/393 | chr2 | 241651022 | ||
chr2:241653596
|
G | A | 1 | a0005 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.269G>A | p.Arg90Gln | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/13 | 291/2797 | 269/1182 | 90/393 | chr2 | 241653596 | ||
chr2:241670757
|
A | G | 2 | a0003a0006 | 26 | HG01099.hp1 HG01515.hp1 HG02056.hp2 others(23): Show |
missense_variant | MODERATE | c.989A>G | p.Asn330Ser | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/13 | 1011/2797 | 989/1182 | 330/393 | chr2 | 241670757 | ||
chr2:241671358
|
T | A | 5 | a0001a0003a0004others(2): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
missense_variant | MODERATE | c.1061T>A | p.Leu354Gln | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/13 | 1083/2797 | 1061/1182 | 354/393 | chr2 | 241671358 | ||
chr2:241671379
|
G | T | 1 | a0006 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1082G>T | p.Cys361Phe | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/13 | 1104/2797 | 1082/1182 | 361/393 | chr2 | 241671379 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241654571
|
G | A | 1 | a0001c0006 | 4 | HG01109.hp1 HG01496.hp2 HG02615.hp1 others(1): Show |
synonymous_variant | LOW | c.309G>A | p.Arg103Arg | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/13 | 331/2797 | 309/1182 | 103/393 | chr2 | 241654571 | ||
chr2:241666718
|
C | T | 2 | a0001c0007a0003c0008 | 6 | HG02074.hp2 HG03209.hp1 NA18906.hp1 others(3): Show |
synonymous_variant | LOW | c.612C>T | p.Asn204Asn | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/13 | 634/2797 | 612/1182 | 204/393 | chr2 | 241666718 | ||
chr2:241666760
|
A | G | 1 | a0001c0005 | 5 | HG02080.hp1 NA18939.hp1 NA18954.hp1 others(2): Show |
synonymous_variant | LOW | c.654A>G | p.Pro218Pro | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/13 | 676/2797 | 654/1182 | 218/393 | chr2 | 241666760 | ||
chr2:241671314
|
G | A | 1 | a0001c0010 | 1 | HG03017.hp1 | splice_region_variant&synonymous_variant | LOW | c.1017G>A | p.Leu339Leu | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/13 | 1039/2797 | 1017/1182 | 339/393 | chr2 | 241671314 | ||
chr2:241671323
|
T | C | 5 | a0001c0002a0001c0005a0001c0006others(2): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
synonymous_variant | LOW | c.1026T>C | p.Leu342Leu | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/13 | 1048/2797 | 1026/1182 | 342/393 | chr2 | 241671323 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241637703
|
C | T | 1 | a0001c0002t0022 | 2 | HG00438.hp1 NA19064.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-12C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/13 | chr2 | 241637703 | ||||||
chr2:241672491
|
C | T | 1 | a0001c0002t0044 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 227 | chr2 | 241672491 | |||||
chr2:241672519
|
T | C | 34 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(31): Show | 254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*255T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 255 | chr2 | 241672519 | |||||
chr2:241672543
|
G | A | 1 | a0001c0002t0023 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 279 | chr2 | 241672543 | |||||
chr2:241672584
|
C | T | 7 | a0001c0002t0005a0001c0002t0013a0001c0002t0022others(4): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*320C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 320 | chr2 | 241672584 | |||||
chr2:241672648
|
T | TG | 30 | a0001c0001t0001a0001c0001t0011a0001c0001t0028others(27): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*387dupG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 388 | INFO_REALIGN_3_PRIME | chr2 | 241672648 | ||||
chr2:241672716
|
T | C | 1 | a0003c0004t0024 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 452 | chr2 | 241672716 | |||||
chr2:241672736
|
C | T | 1 | a0001c0002t0015 | 3 | HG01496.hp1 NA20805.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*472C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 472 | chr2 | 241672736 | |||||
chr2:241672766
|
C | T | 1 | a0003c0004t0034 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*502C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 502 | chr2 | 241672766 | |||||
chr2:241672927
|
G | T | 31 | a0001c0001t0001a0001c0001t0011a0001c0001t0021others(28): Show | 227 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*663G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 663 | chr2 | 241672927 | |||||
chr2:241673040
|
CG | C | 9 | a0001c0001t0004a0001c0001t0020a0001c0001t0032others(6): Show | 68 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*786delG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 786 | INFO_REALIGN_3_PRIME | chr2 | 241673040 | ||||
chr2:241673040
|
CGG | C | 41 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(38): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*785_*786delGG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 785 | INFO_REALIGN_3_PRIME | chr2 | 241673040 | ||||
chr2:241673045
|
G | C | 1 | a0001c0002t0025 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*781G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 781 | chr2 | 241673045 | |||||
chr2:241673072
|
C | T | 30 | a0001c0001t0001a0001c0001t0011a0001c0001t0028others(27): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*808C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 808 | chr2 | 241673072 | |||||
chr2:241673140
|
G | C | 1 | a0002c0003t0043 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*876G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 876 | chr2 | 241673140 | |||||
chr2:241673152
|
C | T | 4 | a0001c0001t0039a0001c0001t0040a0001c0002t0013others(1): Show | 6 | HG00597.hp1 HG00621.hp2 HG02135.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*888C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 888 | chr2 | 241673152 | |||||
chr2:241673203
|
TGTG | T | 3 | a0001c0001t0006a0001c0001t0009a0001c0001t0018 | 27 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*943_*945delGTG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 943 | INFO_REALIGN_3_PRIME | chr2 | 241673203 | ||||
chr2:241673340
|
G | A | 12 | a0001c0001t0001a0001c0001t0028a0001c0001t0032others(9): Show | 117 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1076G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1076 | chr2 | 241673340 | |||||
chr2:241673342
|
T | G | 1 | a0001c0001t0039 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1078T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1078 | chr2 | 241673342 | |||||
chr2:241673369
|
T | G | 30 | a0001c0001t0001a0001c0001t0011a0001c0001t0017others(27): Show | 227 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*1105T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1105 | chr2 | 241673369 | |||||
chr2:241673415
|
G | A | 3 | a0001c0001t0006a0001c0001t0009a0001c0001t0016 | 28 | HG01167.hp2 HG01169.hp1 HG01261.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1151G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1151 | chr2 | 241673415 | |||||
chr2:241673420
|
T | C | 15 | a0001c0002t0003a0001c0002t0005a0001c0002t0013others(12): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1156T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1156 | chr2 | 241673420 | |||||
chr2:241673457
|
C | CGCT | 15 | a0001c0002t0003a0001c0002t0005a0001c0002t0013others(12): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1209_*1211dupGCT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1212 | INFO_REALIGN_3_PRIME | chr2 | 241673457 | ||||
chr2:241673485
|
C | T | 1 | a0001c0001t0028 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1221C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1221 | chr2 | 241673485 | |||||
chr2:241673493
|
C | T | 1 | a0001c0001t0018 | 2 | HG03453.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1229C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1229 | chr2 | 241673493 | |||||
chr2:241673494
|
A | G | 34 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(31): Show | 256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*1230A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1230 | chr2 | 241673494 | |||||
chr2:241673504
|
G | A | 1 | a0001c0002t0029 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1240 | chr2 | 241673504 | |||||
chr2:241673583
|
CAT | C | 8 | a0001c0001t0002a0001c0001t0020a0001c0001t0021others(5): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1321_*1322delTA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1321 | INFO_REALIGN_3_PRIME | chr2 | 241673583 | ||||
chr2:241673598
|
C | G | 1 | a0001c0001t0037 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1334C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1334 | chr2 | 241673598 | |||||
chr2:241673674
|
A | G | 27 | a0001c0001t0001a0001c0001t0011a0001c0001t0017others(24): Show | 206 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1410A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1410 | chr2 | 241673674 | |||||
chr2:241673718
|
T | G | 30 | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(27): Show | 233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*1454T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1454 | chr2 | 241673718 | |||||
chr2:241673763
|
T | G | 1 | a0001c0002t0035 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1499T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1499 | chr2 | 241673763 | |||||
chr2:241673812
|
G | A | 1 | a0003c0004t0026 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1548G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 13/13 | 1548 | chr2 | 241673812 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241637840
|
C | T | 2 | a0001c0001t0001g0354a0001c0001t0001g0355 | 2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.10+116C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241637840 | ||||||
chr2:241637872
|
G | GGGGCGGT others(13): Show |
3 | a0002c0003t0014g0351a0002c0003t0014g0352a0002c0003t0014g0353 | 3 | HG00741.hp1 HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.10+157_10+176dupTT others(18): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241637872 | |||||
chr2:241637943
|
C | T | 1 | a0001c0001t0001g0350 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10+219C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241637943 | ||||||
chr2:241638014
|
C | CCCTTGCG others(26): Show |
1 | a0001c0001t0001g0349 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.10+299_10+300insTC others(31): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241638014 | |||||
chr2:241638059
|
G | C | 1 | a0001c0001t0001g0349 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.10+335G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638059 | ||||||
chr2:241638146
|
G | A | 1 | a0001c0001t0002g0004 | 3 | HG02559.hp1 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.10+422G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638146 | ||||||
chr2:241638147
|
C | A | 1 | a0001c0002t0003g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.10+423C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638147 | ||||||
chr2:241638149
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.10+425T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638149 | ||||||
chr2:241638192
|
G | A | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+468G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638192 | ||||||
chr2:241638250
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(41): Show | 52 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.10+526C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638250 | ||||||
chr2:241638265
|
C | A | 1 | a0001c0002t0003g0043 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.10+541C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638265 | ||||||
chr2:241638370
|
A | AGT | 81 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(78): Show | 88 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.10+661_10+662dupGT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241638370 | |||||
chr2:241638413
|
C | T | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+689C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638413 | ||||||
chr2:241638419
|
A | G | 1 | a0001c0001t0017g0038 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.10+695A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638419 | ||||||
chr2:241638420
|
T | C | 10 | a0002c0003t0008g0005a0002c0003t0008g0044a0002c0003t0008g0045others(7): Show | 12 | NA18946.hp2 NA18949.hp2 NA18957.hp1 others(9): Show |
intron_variant | MODIFIER | c.10+696T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638420 | ||||||
chr2:241638475
|
G | T | 3 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0312 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.10+751G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638475 | ||||||
chr2:241638482
|
C | T | 1 | a0001c0001t0002g0311 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.10+758C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638482 | ||||||
chr2:241638497
|
T | A | 1 | a0001c0001t0001g0349 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.10+773T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638497 | ||||||
chr2:241638498
|
A | T | 1 | a0001c0001t0001g0349 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.10+774A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638498 | ||||||
chr2:241638501
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(39): Show | 49 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.10+777T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638501 | ||||||
chr2:241638535
|
G | A | 152 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0093others(149): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.10+811G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638535 | ||||||
chr2:241638555
|
C | T | 6 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0176others(3): Show | 8 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.10+831C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638555 | ||||||
chr2:241638610
|
T | A | 1 | a0001c0005t0005g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.10+886T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638610 | ||||||
chr2:241638705
|
C | A | 11 | a0001c0002t0005g0014a0001c0002t0005g0060a0001c0002t0005g0061others(8): Show | 12 | HG01952.hp2 HG01981.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.10+981C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638705 | ||||||
chr2:241638722
|
A | G | 1 | a0002c0003t0004g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.10+998A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638722 | ||||||
chr2:241638786
|
C | T | 1 | a0001c0001t0020g0310 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.10+1062C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638786 | ||||||
chr2:241638935
|
G | C | 1 | a0001c0001t0001g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.10+1211G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638935 | ||||||
chr2:241638982
|
C | T | 6 | a0001c0001t0006g0343a0001c0001t0006g0344a0001c0001t0006g0345others(3): Show | 6 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.10+1258C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638982 | ||||||
chr2:241638999
|
C | G | 1 | a0001c0001t0001g0242 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.10+1275C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241638999 | ||||||
chr2:241639127
|
G | T | 1 | a0001c0005t0005g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.10+1403G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639127 | ||||||
chr2:241639166
|
C | T | 1 | a0001c0005t0005g0174 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.10+1442C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639166 | ||||||
chr2:241639174
|
C | G | 153 | a0001c0001t0001g0241a0001c0001t0002g0090a0001c0001t0002g0092others(150): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.10+1450C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639174 | ||||||
chr2:241639226
|
C | T | 1 | a0002c0003t0004g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.10+1502C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639226 | ||||||
chr2:241639230
|
G | A | 8 | a0001c0001t0006g0343a0001c0001t0006g0344a0001c0001t0006g0345others(5): Show | 10 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.10+1506G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639230 | ||||||
chr2:241639246
|
A | G | 1 | a0001c0001t0002g0309 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.10+1522A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639246 | ||||||
chr2:241639335
|
G | T | 153 | a0001c0001t0001g0241a0001c0001t0002g0090a0001c0001t0002g0092others(150): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.10+1611G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639335 | ||||||
chr2:241639386
|
A | C | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+1662A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639386 | ||||||
chr2:241639590
|
G | C | 1 | a0001c0001t0002g0311 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.10+1866G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639590 | ||||||
chr2:241639657
|
G | T | 1 | a0001c0005t0005g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.10+1933G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639657 | ||||||
chr2:241639860
|
G | T | 79 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(76): Show | 86 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.10+2136G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639860 | ||||||
chr2:241639909
|
G | A | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+2185G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639909 | ||||||
chr2:241639992
|
C | G | 1 | a0001c0002t0003g0173 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10+2268C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241639992 | ||||||
chr2:241640076
|
A | G | 2 | a0001c0001t0001g0342a0001c0001t0006g0341 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.10+2352A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640076 | ||||||
chr2:241640242
|
T | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(241): Show | 274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.10+2518T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640242 | ||||||
chr2:241640398
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(39): Show | 49 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.10+2674C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640398 | ||||||
chr2:241640430
|
C | T | 1 | a0001c0002t0003g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.10+2706C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640430 | ||||||
chr2:241640432
|
T | C | 1 | a0001c0002t0003g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.10+2708T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640432 | ||||||
chr2:241640779
|
A | G | 324 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(321): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.10+3055A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640779 | ||||||
chr2:241640787
|
C | CG | 5 | a0001c0001t0001g0211a0001c0002t0003g0069a0001c0002t0013g0068others(2): Show | 5 | HG02135.hp1 NA18959.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.10+3066dupG | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241640787 | |||||
chr2:241640818
|
A | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.10+3094A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640818 | ||||||
chr2:241640836
|
C | T | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.10+3112C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640836 | ||||||
chr2:241640996
|
A | G | 7 | a0001c0001t0006g0172a0001c0001t0009g0023a0001c0001t0009g0024others(4): Show | 9 | HG02647.hp2 NA18960.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.10+3272A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241640996 | ||||||
chr2:241641055
|
G | A | 193 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0002g0090others(190): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.10+3331G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641055 | ||||||
chr2:241641057
|
G | A | 29 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0002g0090others(26): Show | 31 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.10+3333G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641057 | ||||||
chr2:241641201
|
G | A | 1 | a0001c0001t0017g0038 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.10+3477G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641201 | ||||||
chr2:241641317
|
G | A | 115 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0100others(112): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.10+3593G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641317 | ||||||
chr2:241641325
|
C | G | 1 | a0001c0001t0002g0308 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+3601C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641325 | ||||||
chr2:241641325
|
C | T | 1 | a0001c0002t0003g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.10+3601C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641325 | ||||||
chr2:241641326
|
G | C | 1 | a0001c0001t0002g0308 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+3602G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641326 | ||||||
chr2:241641346
|
C | T | 1 | a0001c0001t0002g0307 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.10+3622C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641346 | ||||||
chr2:241641411
|
A | T | 1 | a0002c0003t0004g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10+3687A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641411 | ||||||
chr2:241641448
|
G | A | 1 | a0001c0002t0005g0166 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.10+3724G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641448 | ||||||
chr2:241641448
|
G | C | 1 | a0001c0001t0002g0308 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+3724G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641448 | ||||||
chr2:241641449
|
C | G | 1 | a0001c0001t0002g0308 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+3725C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641449 | ||||||
chr2:241641458
|
G | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.10+3734G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641458 | ||||||
chr2:241641549
|
C | CA | 16 | a0001c0001t0001g0213a0001c0001t0001g0315a0001c0001t0001g0316others(13): Show | 16 | HG00639.hp1 HG02055.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.10+3842dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241641549 | |||||
chr2:241641549
|
C | CAA | 21 | a0001c0002t0003g0188a0001c0005t0005g0198a0001c0005t0005g0199others(18): Show | 23 | HG01515.hp1 HG01884.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.10+3841_10+3842dup others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241641549 | |||||
chr2:241641767
|
G | A | 1 | a0001c0002t0044g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.10+4043G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641767 | ||||||
chr2:241641951
|
A | G | 4 | a0001c0002t0003g0162a0001c0002t0003g0163a0001c0002t0003g0164others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+4227A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241641951 | ||||||
chr2:241642033
|
T | TA | 192 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0093others(189): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.10+4319dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241642033 | |||||
chr2:241642109
|
A | G | 1 | a0001c0010t0002g0306 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.10+4385A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642109 | ||||||
chr2:241642167
|
G | GT | 6 | a0001c0001t0002g0311a0001c0002t0003g0210a0001c0002t0013g0068others(3): Show | 6 | HG02135.hp1 HG03710.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.10+4456dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241642167 | |||||
chr2:241642173
|
TTTTTTTT others(7): Show |
T | 1 | a0001c0001t0002g0308 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10+4451_10+4464del others(14): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241642173 | |||||
chr2:241642188
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(322): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.10+4464T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642188 | ||||||
chr2:241642336
|
T | C | 2 | a0001c0001t0002g0250a0001c0001t0002g0251 | 2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.10+4612T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642336 | ||||||
chr2:241642393
|
T | A | 79 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(76): Show | 86 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.10+4669T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642393 | ||||||
chr2:241642411
|
A | G | 1 | a0001c0001t0011g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10+4687A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642411 | ||||||
chr2:241642495
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.10+4771G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642495 | ||||||
chr2:241642569
|
G | GT | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(272): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.10+4854dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241642569 | |||||
chr2:241642645
|
A | C | 6 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0176others(3): Show | 8 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.10+4921A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642645 | ||||||
chr2:241642830
|
CTAA | C | 81 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(78): Show | 88 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.10+5107_10+5109del others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642830 | ||||||
chr2:241642871
|
C | CT | 80 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0247others(77): Show | 89 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(1): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTT | 44 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0037others(41): Show | 50 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTT | 16 | a0001c0001t0001g0316a0001c0001t0001g0338a0001c0001t0001g0339others(13): Show | 17 | HG00423.hp1 HG01243.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTT | 4 | a0001c0001t0001g0317a0001c0002t0005g0066a0001c0002t0005g0170others(1): Show | 4 | HG02074.hp2 NA18984.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTT | 9 | a0001c0001t0018g0015a0001c0002t0003g0095a0001c0002t0005g0071others(6): Show | 10 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(5): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTT | 57 | a0001c0001t0002g0092a0001c0001t0002g0100a0001c0001t0004g0110others(54): Show | 66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(6): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT | 27 | a0001c0001t0004g0135a0001c0001t0004g0136a0001c0002t0003g0008others(24): Show | 30 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(7): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0004g0143a0001c0001t0004g0145a0001c0001t0006g0007others(11): Show | 16 | HG01099.hp2 HG01167.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(8): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(2): Show |
12 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(9): Show | 12 | HG01169.hp1 HG01433.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(9): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(4): Show |
1 | a0001c0002t0005g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(11): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0005g0076 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(13): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(11): Show |
3 | a0001c0002t0005g0017a0001c0002t0005g0077a0001c0002t0005g0078 | 4 | HG02132.hp2 NA18957.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(18): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(12): Show |
4 | a0001c0002t0003g0173a0001c0002t0005g0080a0001c0002t0013g0079others(1): Show | 4 | HG00597.hp1 NA18969.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(19): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(13): Show |
2 | a0002c0003t0004g0082a0002c0003t0004g0083 | 2 | HG02155.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(20): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(14): Show |
2 | a0001c0002t0005g0084a0001c0002t0013g0068 | 2 | HG02135.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(21): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(15): Show |
3 | a0001c0002t0005g0085a0001c0002t0022g0086a0001c0002t0022g0087 | 3 | HG00438.hp1 HG02129.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.10+5147_10+5148ins others(22): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(16): Show |
1 | a0001c0002t0005g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(23): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(18): Show |
1 | a0001c0002t0013g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(25): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0002g0090 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.10+5147_10+5148ins others(26): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
CCTTTTTT others(2): Show |
C | 25 | a0001c0002t0003g0094a0001c0005t0005g0198a0001c0005t0005g0199others(22): Show | 27 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.10+5148_10+5156del others(9): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642871
|
CCTTTTTT others(3): Show |
C | 3 | a0001c0002t0003g0188a0003c0004t0007g0190a0003c0004t0024g0189 | 3 | HG01943.hp2 HG03041.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.10+5148_10+5157del others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642871 | ||||||
chr2:241642872
|
C | T | 292 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(289): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.10+5148C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642872 | ||||||
chr2:241642972
|
T | C | 1 | a0001c0002t0003g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.10+5248T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241642972 | ||||||
chr2:241643076
|
G | A | 114 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0100others(111): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.10+5352G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643076 | ||||||
chr2:241643165
|
GAACCACC others(6): Show |
G | 1 | a0003c0004t0027g0246 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.10+5446_10+5458del others(13): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643165 | |||||
chr2:241643267
|
C | T | 2 | a0001c0006t0003g0122a0001c0006t0003g0123 | 2 | HG01109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.10+5543C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643267 | ||||||
chr2:241643310
|
T | C | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+5586T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643310 | ||||||
chr2:241643364
|
A | AT | 19 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(16): Show | 20 | HG01175.hp1 HG01175.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.10+5662dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643364 | |||||
chr2:241643364
|
A | ATT | 35 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0037others(32): Show | 39 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.10+5661_10+5662dup others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643364 | |||||
chr2:241643364
|
A | ATTT | 7 | a0001c0001t0001g0003a0001c0001t0001g0316a0001c0001t0001g0337others(4): Show | 10 | HG00423.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.10+5660_10+5662dup others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643364 | |||||
chr2:241643364
|
AT | A | 119 | a0001c0001t0001g0254a0001c0001t0001g0342a0001c0001t0002g0092others(116): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.10+5662delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643364 | |||||
chr2:241643576
|
A | G | 79 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(76): Show | 86 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.10+5852A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643576 | ||||||
chr2:241643596
|
A | G | 28 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(25): Show | 30 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.10+5872A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643596 | ||||||
chr2:241643603
|
CAT | C | 3 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0312 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.10+5887_10+5888del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643603 | |||||
chr2:241643616
|
A | G | 81 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(78): Show | 88 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.10+5892A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643616 | ||||||
chr2:241643619
|
T | G | 4 | a0001c0002t0003g0162a0001c0002t0003g0163a0001c0002t0003g0164others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5895T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643619 | ||||||
chr2:241643663
|
C | CGT | 148 | a0001c0001t0001g0236a0001c0001t0002g0090a0001c0001t0002g0092others(145): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.10+5956_10+5957dup others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | |||||
chr2:241643663
|
C | CGTGT | 10 | a0001c0001t0002g0004a0001c0001t0002g0257a0001c0001t0004g0114others(7): Show | 12 | HG00609.hp2 HG00639.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.10+5954_10+5957dup others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | |||||
chr2:241643663
|
C | CGTGTGT | 75 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(72): Show | 79 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.10+5952_10+5957dup others(6): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | |||||
chr2:241643663
|
C | CGTGTGTG others(1): Show |
10 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0288others(7): Show | 11 | HG00558.hp2 HG00639.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.10+5950_10+5957dup others(8): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | |||||
chr2:241643663
|
C | CGTGTGTG others(3): Show |
28 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(25): Show | 35 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.10+5948_10+5957dup others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | |||||
chr2:241643663
|
C | CGTGTGTG others(5): Show |
8 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0323others(5): Show | 8 | HG00423.hp1 HG01891.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.10+5946_10+5957dup others(12): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | |||||
chr2:241643663
|
C | CGTGTGTG others(7): Show |
1 | a0001c0001t0001g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.10+5944_10+5957dup others(14): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | |||||
chr2:241643663
|
CGT | C | 25 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(22): Show | 27 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.10+5956_10+5957del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | |||||
chr2:241643663
|
CGTGT | C | 4 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0312others(1): Show | 4 | HG02818.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5954_10+5957del others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643663 | |||||
chr2:241643678
|
G | GTGTGTGT others(3): Show |
7 | a0001c0001t0006g0343a0001c0001t0006g0344a0001c0001t0006g0345others(4): Show | 8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.10+5957_10+5958ins others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643678 | |||||
chr2:241643688
|
A | T | 1 | a0002c0003t0008g0045 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.10+5964A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643688 | ||||||
chr2:241643690
|
A | AT | 4 | a0001c0002t0003g0098a0001c0002t0003g0099a0002c0003t0008g0045others(1): Show | 4 | HG00597.hp2 HG03834.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.10+5970dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643690 | |||||
chr2:241643690
|
AT | A | 9 | a0001c0001t0001g0216a0001c0001t0006g0343a0001c0001t0006g0344others(6): Show | 10 | HG01099.hp1 HG02055.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.10+5970delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643690 | |||||
chr2:241643692
|
T | TCCCCCCC others(3): Show |
4 | a0001c0005t0005g0199a0003c0004t0007g0026a0003c0004t0007g0207others(1): Show | 5 | HG02056.hp2 HG03041.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.10+5968_10+5969ins others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | ||||||
chr2:241643692
|
T | TCCCCCCC others(4): Show |
4 | a0001c0005t0005g0180a0001c0005t0005g0198a0003c0004t0007g0196others(1): Show | 4 | HG06807.hp1 NA18955.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+5968_10+5969ins others(11): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | ||||||
chr2:241643692
|
T | TCCCCCCC others(5): Show |
1 | a0003c0004t0010g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.10+5968_10+5969ins others(12): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | ||||||
chr2:241643692
|
T | TCCCCCCC others(7): Show |
5 | a0001c0002t0003g0188a0001c0005t0005g0203a0003c0004t0007g0191others(2): Show | 5 | HG01515.hp1 HG01943.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.10+5968_10+5969ins others(14): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | ||||||
chr2:241643692
|
T | TCCCCCCC others(14): Show |
3 | a0003c0004t0007g0193a0003c0004t0010g0192a0003c0004t0010g0205 | 3 | HG02647.hp1 NA19030.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.10+5968_10+5969ins others(21): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | ||||||
chr2:241643692
|
T | TCCCCCCC others(15): Show |
1 | a0001c0006t0003g0204 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.10+5968_10+5969ins others(22): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | ||||||
chr2:241643692
|
T | TCCCCCCC others(36): Show |
1 | a0003c0004t0027g0246 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.10+5968_10+5969ins others(43): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | ||||||
chr2:241643692
|
TTTCC | T | 4 | a0003c0004t0010g0027a0003c0004t0010g0028a0003c0004t0010g0201others(1): Show | 5 | HG02559.hp2 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.10+5969_10+5972del others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643692 | ||||||
chr2:241643693
|
T | C | 23 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(20): Show | 24 | HG01496.hp2 HG01515.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.10+5969T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643693 | ||||||
chr2:241643694
|
T | C | 29 | a0001c0001t0001g0215a0001c0001t0001g0313a0001c0001t0001g0314others(26): Show | 30 | HG00738.hp2 HG01099.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.10+5970T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643694 | ||||||
chr2:241643694
|
TC | T | 108 | a0001c0001t0002g0090a0001c0001t0002g0093a0001c0001t0004g0110others(105): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.10+5981delC | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643694 | |||||
chr2:241643694
|
TCC | T | 82 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(79): Show | 89 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.10+5980_10+5981del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241643694 | |||||
chr2:241643695
|
C | T | 50 | a0001c0001t0002g0092a0001c0001t0002g0100a0001c0001t0004g0114others(47): Show | 58 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.10+5971C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643695 | ||||||
chr2:241643696
|
C | T | 109 | a0001c0001t0002g0090a0001c0001t0002g0093a0001c0001t0004g0110others(106): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.10+5972C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643696 | ||||||
chr2:241643699
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.10+5975C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643699 | ||||||
chr2:241643738
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(39): Show | 49 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.10+6014C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643738 | ||||||
chr2:241643788
|
C | G | 1 | a0001c0002t0013g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.10+6064C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643788 | ||||||
chr2:241643812
|
C | G | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+6088C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643812 | ||||||
chr2:241643843
|
G | A | 5 | a0001c0002t0005g0166a0001c0002t0005g0167a0001c0002t0005g0168others(2): Show | 5 | NA18942.hp1 NA18953.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.10+6119G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643843 | ||||||
chr2:241643879
|
G | A | 78 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(75): Show | 85 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.10+6155G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643879 | ||||||
chr2:241643929
|
A | C | 4 | a0001c0005t0005g0180a0001c0005t0005g0198a0001c0005t0005g0199others(1): Show | 4 | NA18939.hp1 NA18954.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.10+6205A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643929 | ||||||
chr2:241643942
|
C | T | 191 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0093others(188): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.10+6218C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643942 | ||||||
chr2:241643943
|
G | A | 2 | a0001c0001t0002g0258a0001c0001t0002g0309 | 2 | HG00408.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.10+6219G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241643943 | ||||||
chr2:241644045
|
A | T | 191 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0093others(188): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.10+6321A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644045 | ||||||
chr2:241644138
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(39): Show | 49 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.10+6414G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644138 | ||||||
chr2:241644241
|
G | A | 1 | a0002c0003t0014g0202 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.10+6517G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644241 | ||||||
chr2:241644285
|
G | A | 191 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0093others(188): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.10+6561G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644285 | ||||||
chr2:241644297
|
C | A | 1 | a0001c0001t0002g0311 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.10+6573C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644297 | ||||||
chr2:241644314
|
G | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(39): Show | 49 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.10+6590G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644314 | ||||||
chr2:241644350
|
C | T | 1 | a0001c0001t0002g0004 | 3 | HG02559.hp1 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.10+6626C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644350 | ||||||
chr2:241644360
|
C | T | 1 | a0002c0003t0004g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.10+6636C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644360 | ||||||
chr2:241644363
|
T | C | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10+6639T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644363 | ||||||
chr2:241644537
|
C | T | 41 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(38): Show | 48 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.11-6473C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644537 | ||||||
chr2:241644538
|
G | A | 3 | a0001c0001t0002g0100a0001c0001t0006g0345a0001c0001t0006g0346 | 3 | HG02486.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.11-6472G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644538 | ||||||
chr2:241644747
|
C | T | 163 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0093others(160): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.11-6263C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644747 | ||||||
chr2:241644864
|
G | A | 1 | a0001c0002t0003g0182 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.11-6146G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241644864 | ||||||
chr2:241644947
|
C | CA | 108 | a0001c0001t0001g0218a0001c0001t0002g0092a0001c0001t0002g0093others(105): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.11-6050dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241644947 | |||||
chr2:241645028
|
T | G | 1 | a0001c0002t0044g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.11-5982T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645028 | ||||||
chr2:241645093
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.11-5917G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645093 | ||||||
chr2:241645218
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(16): Show | 25 | HG00735.hp2 HG00738.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.11-5792C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645218 | ||||||
chr2:241645327
|
G | C | 1 | a0006c0011t0007g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.11-5683G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645327 | ||||||
chr2:241645335
|
A | G | 28 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(25): Show | 30 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.11-5675A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645335 | ||||||
chr2:241645424
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.11-5586A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645424 | ||||||
chr2:241645461
|
T | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(46): Show | 57 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.11-5549T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645461 | ||||||
chr2:241645483
|
C | T | 1 | a0002c0003t0042g0142 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.11-5527C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645483 | ||||||
chr2:241645487
|
C | T | 1 | a0001c0002t0003g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.11-5523C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645487 | ||||||
chr2:241645505
|
A | G | 159 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0093others(156): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.11-5505A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645505 | ||||||
chr2:241645599
|
C | T | 2 | a0001c0001t0001g0342a0001c0001t0006g0341 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.11-5411C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645599 | ||||||
chr2:241645626
|
C | T | 1 | a0001c0001t0017g0038 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.11-5384C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645626 | ||||||
chr2:241645729
|
C | T | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.11-5281C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645729 | ||||||
chr2:241645736
|
CACAGT | C | 6 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0176others(3): Show | 8 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.11-5271_11-5267del others(5): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241645736 | |||||
chr2:241645888
|
A | G | 26 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(23): Show | 28 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.11-5122A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645888 | ||||||
chr2:241645940
|
T | C | 1 | a0001c0002t0005g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.11-5070T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645940 | ||||||
chr2:241645954
|
G | A | 41 | a0001c0001t0004g0110a0001c0002t0003g0021a0001c0002t0003g0091others(38): Show | 47 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.11-5056G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645954 | ||||||
chr2:241645960
|
C | T | 3 | a0001c0001t0038g0158a0003c0008t0019g0041a0003c0008t0019g0042 | 3 | HG03209.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.11-5050C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241645960 | ||||||
chr2:241646201
|
G | A | 244 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(241): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.11-4809G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646201 | ||||||
chr2:241646219
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0037others(27): Show | 36 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.11-4791G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646219 | ||||||
chr2:241646306
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0319a0001c0001t0001g0321others(2): Show | 6 | HG01106.hp2 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.11-4704A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646306 | ||||||
chr2:241646319
|
C | G | 2 | a0001c0007t0005g0059a0001c0007t0005g0067 | 2 | NA18946.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.11-4691C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646319 | ||||||
chr2:241646394
|
G | C | 1 | a0002c0003t0004g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.11-4616G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646394 | ||||||
chr2:241646408
|
C | G | 1 | a0001c0001t0001g0233 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.11-4602C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646408 | ||||||
chr2:241646461
|
A | G | 1 | a0002c0003t0004g0030 | 2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.11-4549A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646461 | ||||||
chr2:241646491
|
C | A | 1 | a0001c0002t0005g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.11-4519C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646491 | ||||||
chr2:241646573
|
C | T | 2 | a0001c0002t0003g0129a0001c0002t0003g0137 | 2 | HG00609.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.11-4437C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646573 | ||||||
chr2:241646735
|
A | G | 2 | a0002c0003t0004g0112a0002c0003t0004g0133 | 2 | NA18954.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.11-4275A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646735 | ||||||
chr2:241646781
|
C | CT | 7 | a0001c0001t0001g0213a0001c0001t0001g0232a0001c0001t0002g0243others(4): Show | 8 | HG01928.hp2 HG01952.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.11-4210dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241646781 | |||||
chr2:241646781
|
CT | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(78): Show | 91 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.11-4210delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241646781 | |||||
chr2:241646781
|
CTT | C | 237 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(234): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.11-4211_11-4210del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241646781 | |||||
chr2:241646837
|
C | A | 1 | a0001c0001t0006g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.11-4173C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646837 | ||||||
chr2:241646845
|
C | T | 3 | a0001c0001t0016g0159a0001c0001t0016g0160a0001c0001t0016g0161 | 3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.11-4165C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241646845 | ||||||
chr2:241647029
|
C | G | 1 | a0001c0002t0005g0078 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.11-3981C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647029 | ||||||
chr2:241647030
|
C | T | 1 | a0002c0003t0004g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.11-3980C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647030 | ||||||
chr2:241647075
|
T | C | 1 | a0001c0002t0003g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.11-3935T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647075 | ||||||
chr2:241647078
|
C | T | 1 | a0003c0008t0019g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.11-3932C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647078 | ||||||
chr2:241647188
|
G | C | 1 | a0003c0004t0010g0197 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.11-3822G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647188 | ||||||
chr2:241647270
|
CATG | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(39): Show | 49 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.11-3738_11-3736del others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241647270 | |||||
chr2:241647297
|
T | C | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.11-3713T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647297 | ||||||
chr2:241647357
|
G | A | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.11-3653G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647357 | ||||||
chr2:241647389
|
C | G | 1 | a0001c0001t0001g0290 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.11-3621C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647389 | ||||||
chr2:241647390
|
G | C | 1 | a0001c0001t0001g0290 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.11-3620G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647390 | ||||||
chr2:241647423
|
C | A | 10 | a0001c0002t0003g0018a0001c0002t0003g0069a0001c0002t0003g0098others(7): Show | 11 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.11-3587C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647423 | ||||||
chr2:241647445
|
C | A | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.11-3565C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647445 | ||||||
chr2:241647482
|
G | A | 242 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(239): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.11-3528G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647482 | ||||||
chr2:241647622
|
CA | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(79): Show | 93 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.11-3367delA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241647622 | |||||
chr2:241647622
|
CAA | C | 227 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(224): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.11-3368_11-3367del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241647622 | |||||
chr2:241647622
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0006g0345a0001c0001t0006g0346a0001c0001t0006g0347others(2): Show | 6 | HG02055.hp1 HG02965.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.11-3378_11-3367del others(12): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241647622 | |||||
chr2:241647639
|
A | G | 193 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(190): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.11-3371A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647639 | ||||||
chr2:241647769
|
G | C | 4 | a0001c0007t0005g0058a0001c0007t0005g0059a0001c0007t0005g0065others(1): Show | 4 | HG02074.hp2 NA18946.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.11-3241G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647769 | ||||||
chr2:241647820
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.11-3190A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647820 | ||||||
chr2:241647836
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(39): Show | 49 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.11-3174G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647836 | ||||||
chr2:241647930
|
A | G | 48 | a0001c0001t0002g0092a0001c0001t0002g0100a0001c0001t0004g0114others(45): Show | 56 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.11-3080A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647930 | ||||||
chr2:241647941
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | NA18612.hp1 NA18963.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.11-3069C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241647941 | ||||||
chr2:241648019
|
C | T | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.11-2991C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648019 | ||||||
chr2:241648245
|
C | A | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.11-2765C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648245 | ||||||
chr2:241648388
|
G | A | 1 | a0001c0002t0003g0188 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.11-2622G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648388 | ||||||
chr2:241648427
|
T | C | 1 | a0003c0004t0010g0197 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.11-2583T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648427 | ||||||
chr2:241648594
|
C | CA | 243 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(240): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.11-2404dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241648594 | |||||
chr2:241648606
|
A | G | 1 | a0003c0004t0027g0246 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.11-2404A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648606 | ||||||
chr2:241648607
|
G | A | 1 | a0003c0004t0027g0246 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.11-2403G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648607 | ||||||
chr2:241648607
|
G | GA | 26 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(23): Show | 28 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.11-2394dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241648607 | |||||
chr2:241648616
|
A | AG | 5 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0176others(2): Show | 7 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.11-2394_11-2393ins others(1): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648616 | ||||||
chr2:241648655
|
G | C | 1 | a0001c0001t0001g0254 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.11-2355G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648655 | ||||||
chr2:241648838
|
T | A | 194 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(191): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.11-2172T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648838 | ||||||
chr2:241648977
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.11-2033C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648977 | ||||||
chr2:241648999
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.11-2011T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241648999 | ||||||
chr2:241649211
|
T | C | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.11-1799T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649211 | ||||||
chr2:241649392
|
T | C | 1 | a0001c0002t0003g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.11-1618T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649392 | ||||||
chr2:241649403
|
T | C | 2 | a0001c0001t0001g0342a0001c0001t0006g0341 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.11-1607T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649403 | ||||||
chr2:241649563
|
C | A | 1 | a0001c0002t0003g0105 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.11-1447C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649563 | ||||||
chr2:241649603
|
C | A | 1 | a0001c0001t0001g0350 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11-1407C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649603 | ||||||
chr2:241649759
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.11-1251T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241649759 | ||||||
chr2:241649784
|
C | CT | 23 | a0001c0001t0001g0029a0001c0001t0001g0213a0001c0001t0001g0215others(20): Show | 25 | HG00099.hp1 HG00738.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.11-1210dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241649784 | |||||
chr2:241650035
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.11-975C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650035 | ||||||
chr2:241650119
|
C | T | 5 | a0001c0001t0002g0034a0001c0001t0002g0257a0001c0001t0002g0283others(2): Show | 6 | HG00099.hp1 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.11-891C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650119 | ||||||
chr2:241650199
|
C | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0319a0001c0001t0001g0321others(4): Show | 8 | HG01074.hp1 HG01106.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.11-811C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650199 | ||||||
chr2:241650225
|
T | C | 4 | a0001c0002t0003g0162a0001c0002t0003g0163a0001c0002t0003g0164others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.11-785T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650225 | ||||||
chr2:241650442
|
G | T | 2 | a0001c0001t0001g0342a0001c0001t0006g0341 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.11-568G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650442 | ||||||
chr2:241650446
|
C | T | 196 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(193): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.11-564C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650446 | ||||||
chr2:241650630
|
T | C | 5 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0342others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.11-380T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650630 | ||||||
chr2:241650636
|
C | T | 5 | a0003c0004t0007g0026a0003c0004t0007g0194a0003c0004t0007g0196others(2): Show | 6 | HG02056.hp2 NA18959.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.11-374C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650636 | ||||||
chr2:241650637
|
G | A | 1 | a0001c0001t0001g0354 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.11-373G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650637 | ||||||
chr2:241650639
|
G | T | 11 | a0001c0002t0003g0008a0001c0002t0003g0025a0001c0002t0003g0182others(8): Show | 14 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.11-371G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650639 | ||||||
chr2:241650684
|
A | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0319a0001c0001t0001g0321others(4): Show | 8 | HG01074.hp1 HG01106.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.11-326A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650684 | ||||||
chr2:241650822
|
T | C | 272 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(269): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.11-188T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650822 | ||||||
chr2:241650914
|
G | A | 1 | a0001c0001t0006g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.11-96G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650914 | ||||||
chr2:241650923
|
A | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(46): Show | 57 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.11-87A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 1/12 | chr2 | 241650923 | ||||||
chr2:241651251
|
A | T | 1 | a0001c0001t0002g0282 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.113-13A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 2/12 | chr2 | 241651251 | ||||||
chr2:241651407
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.184+72A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651407 | ||||||
chr2:241651433
|
C | T | 1 | a0001c0002t0003g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.184+98C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651433 | ||||||
chr2:241651652
|
G | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0295 | 2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.184+317G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651652 | ||||||
chr2:241651658
|
G | A | 1 | a0001c0002t0003g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.184+323G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651658 | ||||||
chr2:241651811
|
C | T | 1 | a0003c0004t0007g0196 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.184+476C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651811 | ||||||
chr2:241651813
|
G | A | 1 | a0001c0001t0002g0261 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.184+478G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651813 | ||||||
chr2:241651941
|
C | T | 1 | a0001c0001t0017g0038 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.184+606C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651941 | ||||||
chr2:241651992
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.184+657G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241651992 | ||||||
chr2:241652013
|
G | A | 7 | a0001c0001t0006g0343a0001c0001t0006g0344a0001c0001t0006g0345others(4): Show | 8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.184+678G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652013 | ||||||
chr2:241652053
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.184+718T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652053 | ||||||
chr2:241652118
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.184+783G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652118 | ||||||
chr2:241652126
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.184+791C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652126 | ||||||
chr2:241652173
|
G | A | 3 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0312 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.184+838G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652173 | ||||||
chr2:241652301
|
C | T | 1 | a0003c0004t0010g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.184+966C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652301 | ||||||
chr2:241652559
|
G | A | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.185-953G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652559 | ||||||
chr2:241652656
|
C | G | 1 | a0001c0007t0005g0058 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.185-856C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652656 | ||||||
chr2:241652691
|
G | A | 1 | a0003c0004t0010g0197 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.185-821G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652691 | ||||||
chr2:241652691
|
G | T | 1 | a0001c0001t0017g0038 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.185-821G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652691 | ||||||
chr2:241652895
|
G | T | 5 | a0001c0002t0005g0071a0001c0002t0005g0072a0001c0002t0005g0085others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-617G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652895 | ||||||
chr2:241652932
|
C | T | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.185-580C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652932 | ||||||
chr2:241652968
|
A | G | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.185-544A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652968 | ||||||
chr2:241652989
|
C | T | 1 | a0001c0001t0001g0338 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.185-523C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652989 | ||||||
chr2:241652999
|
A | C | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.185-513A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241652999 | ||||||
chr2:241653005
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.185-507C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653005 | ||||||
chr2:241653038
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-474C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653038 | ||||||
chr2:241653176
|
A | G | 42 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.185-336A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653176 | ||||||
chr2:241653221
|
C | T | 3 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0312 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.185-291C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653221 | ||||||
chr2:241653227
|
G | A | 2 | a0001c0001t0001g0342a0001c0001t0006g0341 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.185-285G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653227 | ||||||
chr2:241653407
|
G | A | 1 | a0003c0004t0007g0190 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.185-105G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653407 | ||||||
chr2:241653506
|
C | T | 1 | a0003c0008t0019g0042 | 1 | HG03209.hp1 | splice_region_variant&intron_variant | LOW | c.185-6C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 3/12 | chr2 | 241653506 | ||||||
chr2:241653644
|
C | T | 1 | a0001c0001t0009g0024 | 2 | NA18971.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.283+34C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653644 | ||||||
chr2:241653678
|
C | T | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283+68C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653678 | ||||||
chr2:241653699
|
A | G | 46 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(43): Show | 53 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.283+89A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653699 | ||||||
chr2:241653703
|
G | A | 1 | a0001c0002t0005g0061 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.283+93G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653703 | ||||||
chr2:241653862
|
C | T | 3 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0312 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.283+252C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653862 | ||||||
chr2:241653947
|
C | G | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.283+337C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653947 | ||||||
chr2:241653947
|
C | T | 1 | a0001c0001t0039g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+337C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653947 | ||||||
chr2:241653990
|
G | GA | 50 | a0001c0001t0001g0232a0001c0001t0002g0263a0001c0001t0002g0264others(47): Show | 57 | HG00140.hp1 HG00438.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.283+401dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241653990 | |||||
chr2:241653990
|
GA | G | 37 | a0001c0001t0001g0213a0001c0001t0001g0217a0001c0001t0001g0230others(34): Show | 38 | HG00323.hp2 HG01099.hp1 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.283+401delA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241653990 | |||||
chr2:241653992
|
A | G | 1 | a0001c0002t0044g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.283+382A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241653992 | ||||||
chr2:241654009
|
A | AG | 5 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0176others(2): Show | 7 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+399_283+400ins others(1): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654009 | ||||||
chr2:241654009
|
A | G | 5 | a0001c0001t0002g0239a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG02074.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+399A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654009 | ||||||
chr2:241654009
|
AAAG | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0037others(23): Show | 31 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.283+411_283+413del others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654009 | |||||
chr2:241654010
|
AAG | A | 9 | a0001c0001t0001g0329a0001c0001t0006g0343a0001c0001t0006g0344others(6): Show | 11 | HG00642.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+402_283+403del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654010 | |||||
chr2:241654014
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.283+404A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654014 | ||||||
chr2:241654148
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.284-398T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654148 | ||||||
chr2:241654150
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.284-396T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654150 | ||||||
chr2:241654160
|
C | G | 1 | a0001c0001t0002g0287 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.284-386C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654160 | ||||||
chr2:241654160
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0222a0001c0001t0001g0241 | 3 | HG01168.hp1 HG01258.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.284-386C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654160 | ||||||
chr2:241654252
|
C | T | 1 | a0001c0001t0002g0276 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.284-294C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654252 | ||||||
chr2:241654264
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(127): Show | 144 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.284-282C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654264 | ||||||
chr2:241654282
|
T | A | 1 | a0001c0005t0005g0174 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.284-264T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654282 | ||||||
chr2:241654288
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(124): Show | 141 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.284-258A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654288 | ||||||
chr2:241654290
|
A | G | 10 | a0001c0005t0005g0180a0001c0005t0005g0198a0001c0005t0005g0199others(7): Show | 11 | HG02056.hp2 NA18939.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-256A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654290 | ||||||
chr2:241654376
|
A | G | 1 | a0001c0002t0044g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.284-170A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654376 | ||||||
chr2:241654392
|
T | G | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.284-154T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654392 | ||||||
chr2:241654419
|
TA | T | 170 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0221others(167): Show | 191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.284-104delA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | |||||
chr2:241654419
|
TAA | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(54): Show | 64 | HG00423.hp1 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.284-105_284-104del others(2): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | |||||
chr2:241654419
|
TAAA | T | 19 | a0001c0001t0001g0317a0001c0001t0006g0345a0001c0001t0006g0346others(16): Show | 21 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-106_284-104del others(3): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | |||||
chr2:241654419
|
TAAAA | T | 39 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(36): Show | 41 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.284-107_284-104del others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | |||||
chr2:241654419
|
TAAAAAAA | T | 16 | a0001c0005t0005g0198a0001c0005t0005g0199a0003c0004t0007g0026others(13): Show | 18 | HG02056.hp2 HG02559.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.284-110_284-104del others(7): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 241654419 | |||||
chr2:241654462
|
A | G | 47 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(44): Show | 50 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.284-84A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 4/12 | chr2 | 241654462 | ||||||
chr2:241654683
|
G | A | 60 | a0001c0001t0002g0033a0001c0001t0002g0040a0001c0001t0002g0255others(57): Show | 63 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.385+36G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654683 | ||||||
chr2:241654802
|
C | T | 6 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0176others(3): Show | 8 | NA18960.hp1 NA18971.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.385+155C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654802 | ||||||
chr2:241654811
|
C | T | 31 | a0001c0001t0006g0147a0001c0001t0011g0036a0001c0001t0011g0328others(28): Show | 34 | HG00642.hp1 HG01099.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.385+164C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654811 | ||||||
chr2:241654825
|
C | T | 1 | a0001c0002t0005g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.385+178C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654825 | ||||||
chr2:241654860
|
C | T | 84 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0247others(81): Show | 90 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.385+213C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241654860 | ||||||
chr2:241655006
|
C | T | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.386-265C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241655006 | ||||||
chr2:241655093
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.386-178C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241655093 | ||||||
chr2:241655095
|
T | C | 68 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0003g0188others(65): Show | 72 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.386-176T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241655095 | ||||||
chr2:241655207
|
C | T | 109 | a0001c0001t0002g0092a0001c0001t0002g0100a0001c0001t0004g0110others(106): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.386-64C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 5/12 | chr2 | 241655207 | ||||||
chr2:241655483
|
G | A | 1 | a0002c0003t0008g0048 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.458+140G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241655483 | ||||||
chr2:241655597
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.458+254C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241655597 | ||||||
chr2:241655789
|
T | C | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.458+446T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241655789 | ||||||
chr2:241655967
|
C | T | 1 | a0001c0001t0011g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.458+624C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241655967 | ||||||
chr2:241656091
|
G | T | 1 | a0001c0002t0003g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.458+748G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656091 | ||||||
chr2:241656136
|
C | T | 2 | a0001c0002t0005g0014a0001c0002t0005g0066 | 3 | NA18962.hp1 NA18984.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.458+793C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656136 | ||||||
chr2:241656171
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.458+828C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656171 | ||||||
chr2:241656199
|
A | T | 196 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(193): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.458+856A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656199 | ||||||
chr2:241656295
|
G | A | 7 | a0001c0001t0006g0343a0001c0001t0006g0344a0001c0001t0006g0345others(4): Show | 8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.458+952G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656295 | ||||||
chr2:241656472
|
C | A | 5 | a0001c0002t0003g0069a0001c0002t0003g0125a0001c0002t0003g0126others(2): Show | 5 | NA18945.hp2 NA18959.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+1129C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656472 | ||||||
chr2:241656505
|
T | C | 204 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(201): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.458+1162T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656505 | ||||||
chr2:241656586
|
C | T | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.458+1243C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656586 | ||||||
chr2:241656713
|
G | A | 5 | a0001c0002t0005g0166a0001c0002t0005g0167a0001c0002t0005g0168others(2): Show | 5 | NA18942.hp1 NA18953.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.458+1370G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656713 | ||||||
chr2:241656802
|
A | G | 1 | a0001c0001t0001g0331 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.458+1459A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656802 | ||||||
chr2:241656981
|
T | G | 1 | a0002c0003t0014g0202 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.458+1638T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241656981 | ||||||
chr2:241657009
|
CCTGGGCT others(13): Show |
C | 42 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.458+1667_458+1686d others(22): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657009 | ||||||
chr2:241657024
|
A | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(37): Show | 47 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.458+1681A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657024 | ||||||
chr2:241657028
|
G | T | 1 | a0001c0001t0001g0334 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.458+1685G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657028 | ||||||
chr2:241657056
|
A | G | 321 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(318): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.458+1713A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657056 | ||||||
chr2:241657107
|
C | G | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.458+1764C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657107 | ||||||
chr2:241657255
|
G | A | 1 | a0001c0001t0002g0004 | 3 | HG02559.hp1 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.459-1853G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657255 | ||||||
chr2:241657290
|
CT | C | 7 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0312others(4): Show | 7 | HG02818.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-1804delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 241657290 | |||||
chr2:241657300
|
T | TTG | 40 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(37): Show | 47 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.459-1807_459-1806i others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 241657300 | |||||
chr2:241657392
|
G | A | 42 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.459-1716G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657392 | ||||||
chr2:241657458
|
C | A | 1 | a0001c0002t0003g0105 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.459-1650C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657458 | ||||||
chr2:241657470
|
A | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(37): Show | 47 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.459-1638A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657470 | ||||||
chr2:241657497
|
G | T | 1 | a0001c0001t0002g0311 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.459-1611G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657497 | ||||||
chr2:241657580
|
G | A | 1 | a0001c0002t0044g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.459-1528G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657580 | ||||||
chr2:241657644
|
C | A | 7 | a0001c0001t0006g0248a0001c0001t0009g0023a0001c0001t0009g0024others(4): Show | 9 | HG03209.hp2 NA18960.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-1464C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657644 | ||||||
chr2:241657884
|
G | C | 69 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0003g0188others(66): Show | 73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.459-1224G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657884 | ||||||
chr2:241657903
|
G | C | 321 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(318): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.459-1205G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241657903 | ||||||
chr2:241658139
|
A | G | 33 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0037others(30): Show | 39 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.459-969A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658139 | ||||||
chr2:241658139
|
A | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0319a0001c0001t0001g0321others(4): Show | 8 | HG01074.hp1 HG01106.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-969A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658139 | ||||||
chr2:241658196
|
C | T | 1 | a0001c0002t0003g0184 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.459-912C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658196 | ||||||
chr2:241658203
|
G | T | 7 | a0001c0001t0006g0343a0001c0001t0006g0344a0001c0001t0006g0345others(4): Show | 8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-905G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658203 | ||||||
chr2:241658482
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.459-626T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658482 | ||||||
chr2:241658622
|
T | TCACTGGC others(3): Show |
42 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.459-482_459-473dup others(10): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 241658622 | |||||
chr2:241658850
|
A | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0213others(9): Show | 16 | HG00735.hp2 HG00738.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.459-258A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658850 | ||||||
chr2:241658852
|
G | T | 1 | a0001c0001t0001g0321 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.459-256G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658852 | ||||||
chr2:241658860
|
C | T | 1 | a0001c0001t0006g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.459-248C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658860 | ||||||
chr2:241658922
|
A | C | 1 | a0001c0006t0003g0134 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.459-186A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241658922 | ||||||
chr2:241659002
|
C | T | 2 | a0001c0001t0001g0342a0001c0001t0006g0341 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.459-106C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241659002 | ||||||
chr2:241659003
|
G | A | 86 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(83): Show | 93 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.459-105G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241659003 | ||||||
chr2:241659073
|
A | T | 1 | a0001c0002t0003g0137 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.459-35A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 6/12 | chr2 | 241659073 | ||||||
chr2:241659364
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.538+177C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659364 | ||||||
chr2:241659530
|
C | T | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.538+343C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659530 | ||||||
chr2:241659659
|
C | T | 85 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(82): Show | 92 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.538+472C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659659 | ||||||
chr2:241659780
|
T | C | 324 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(321): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.538+593T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659780 | ||||||
chr2:241659781
|
T | C | 324 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(321): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.538+594T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659781 | ||||||
chr2:241659920
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.538+733G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659920 | ||||||
chr2:241659921
|
G | T | 1 | a0002c0003t0004g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.538+734G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241659921 | ||||||
chr2:241660062
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.538+875C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660062 | ||||||
chr2:241660112
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.538+925C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660112 | ||||||
chr2:241660146
|
C | T | 2 | a0001c0002t0015g0020a0001c0002t0015g0103 | 3 | HG01496.hp1 NA20805.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.538+959C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660146 | ||||||
chr2:241660183
|
C | T | 42 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+996C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660183 | ||||||
chr2:241660232
|
C | T | 7 | a0001c0001t0006g0248a0001c0001t0009g0023a0001c0001t0009g0024others(4): Show | 9 | HG03209.hp2 NA18960.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+1045C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660232 | ||||||
chr2:241660321
|
C | T | 42 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+1134C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660321 | ||||||
chr2:241660354
|
A | G | 360 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(357): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.538+1167A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660354 | ||||||
chr2:241660367
|
C | G | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.538+1180C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660367 | ||||||
chr2:241660390
|
G | A | 5 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0342others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.538+1203G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660390 | ||||||
chr2:241660561
|
T | C | 1 | a0002c0003t0004g0116 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.538+1374T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660561 | ||||||
chr2:241660703
|
T | TA | 42 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+1517dupA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241660703 | |||||
chr2:241660807
|
C | T | 42 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+1620C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660807 | ||||||
chr2:241660941
|
G | C | 1 | a0001c0001t0002g0269 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.538+1754G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660941 | ||||||
chr2:241660968
|
C | T | 2 | a0001c0001t0001g0354a0001c0001t0001g0355 | 2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.538+1781C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241660968 | ||||||
chr2:241661117
|
G | A | 1 | a0006c0011t0007g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538+1930G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661117 | ||||||
chr2:241661237
|
C | G | 1 | a0001c0001t0001g0003 | 4 | HG01884.hp1 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.538+2050C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661237 | ||||||
chr2:241661284
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.538+2097A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661284 | ||||||
chr2:241661430
|
G | T | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.538+2243G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661430 | ||||||
chr2:241661464
|
G | A | 1 | a0003c0004t0010g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.538+2277G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661464 | ||||||
chr2:241661481
|
C | T | 42 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.538+2294C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661481 | ||||||
chr2:241661515
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.538+2328C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661515 | ||||||
chr2:241661573
|
C | T | 1 | a0001c0002t0044g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+2386C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661573 | ||||||
chr2:241661593
|
G | T | 9 | a0001c0001t0006g0248a0001c0001t0009g0023a0001c0001t0009g0024others(6): Show | 11 | HG03209.hp1 HG03209.hp2 NA18906.hp1 others(8): Show |
intron_variant | MODIFIER | c.538+2406G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661593 | ||||||
chr2:241661643
|
C | G | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.538+2456C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661643 | ||||||
chr2:241661653
|
C | T | 1 | a0002c0003t0004g0116 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.538+2466C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661653 | ||||||
chr2:241661757
|
C | T | 1 | a0002c0003t0004g0109 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.538+2570C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661757 | ||||||
chr2:241661834
|
G | A | 1 | a0001c0002t0005g0061 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.538+2647G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661834 | ||||||
chr2:241661871
|
A | C | 1 | a0001c0010t0002g0306 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.538+2684A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241661871 | ||||||
chr2:241662013
|
G | A | 278 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(275): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.538+2826G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662013 | ||||||
chr2:241662098
|
C | G | 1 | a0001c0001t0002g0272 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.538+2911C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662098 | ||||||
chr2:241662199
|
G | A | 199 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(196): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.538+3012G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662199 | ||||||
chr2:241662290
|
G | C | 7 | a0001c0001t0006g0343a0001c0001t0006g0344a0001c0001t0006g0345others(4): Show | 8 | HG02055.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.538+3103G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662290 | ||||||
chr2:241662517
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.538+3330G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662517 | ||||||
chr2:241662553
|
C | T | 1 | a0001c0001t0040g0268 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.538+3366C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662553 | ||||||
chr2:241662698
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.538+3511G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662698 | ||||||
chr2:241662740
|
TGGGCCGG others(46): Show |
T | 3 | a0001c0002t0005g0017a0001c0002t0005g0077a0001c0002t0005g0080 | 4 | NA18957.hp2 NA18975.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+3563_538+3615d others(55): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241662740 | |||||
chr2:241662751
|
TGGTGGCT others(46): Show |
T | 1 | a0001c0002t0005g0084 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.538+3597_538+3649d others(55): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241662751 | |||||
chr2:241662761
|
C | T | 255 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0032others(252): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.538+3574C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662761 | ||||||
chr2:241662787
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.538+3600A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662787 | ||||||
chr2:241662798
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.538+3611C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662798 | ||||||
chr2:241662804
|
C | T | 1 | a0001c0002t0005g0080 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.538+3617C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662804 | ||||||
chr2:241662855
|
C | T | 1 | a0001c0001t0009g0024 | 2 | NA18971.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.538+3668C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662855 | ||||||
chr2:241662857
|
CGGTGGCT others(46): Show |
C | 1 | a0001c0001t0002g0276 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.538+3703_539-3703d others(55): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241662857 | |||||
chr2:241662858
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0349 | 3 | NA19006.hp1 NA19065.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.538+3671G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662858 | ||||||
chr2:241662952
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.539-3693C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662952 | ||||||
chr2:241662953
|
G | A | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.539-3692G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241662953 | ||||||
chr2:241662956
|
C | CCGGGCG | 5 | a0001c0002t0005g0166a0001c0002t0005g0167a0001c0002t0005g0168others(2): Show | 5 | NA18942.hp1 NA18953.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-3685_539-3680d others(8): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241662956 | |||||
chr2:241663054
|
C | T | 90 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0254others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.539-3591C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663054 | ||||||
chr2:241663095
|
T | G | 1 | a0002c0003t0043g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-3550T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663095 | ||||||
chr2:241663097
|
G | T | 1 | a0002c0003t0043g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-3548G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663097 | ||||||
chr2:241663098
|
T | G | 1 | a0002c0003t0043g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-3547T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663098 | ||||||
chr2:241663125
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.539-3520C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663125 | ||||||
chr2:241663126
|
G | A | 1 | a0001c0001t0032g0330 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.539-3519G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663126 | ||||||
chr2:241663140
|
C | T | 1 | a0001c0001t0002g0307 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.539-3505C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663140 | ||||||
chr2:241663175
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.539-3470G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663175 | ||||||
chr2:241663317
|
G | C | 27 | a0001c0002t0003g0188a0001c0005t0005g0180a0001c0005t0005g0198others(24): Show | 29 | HG01099.hp1 HG01515.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.539-3328G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663317 | ||||||
chr2:241663322
|
C | A | 1 | a0002c0003t0004g0117 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.539-3323C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663322 | ||||||
chr2:241663374
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.539-3271G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663374 | ||||||
chr2:241663490
|
G | C | 33 | a0001c0001t0002g0250a0001c0002t0003g0188a0001c0005t0005g0180others(30): Show | 37 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.539-3155G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663490 | ||||||
chr2:241663567
|
T | C | 1 | a0001c0001t0002g0300 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.539-3078T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663567 | ||||||
chr2:241663591
|
T | C | 33 | a0001c0001t0002g0250a0001c0002t0003g0188a0001c0005t0005g0180others(30): Show | 37 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.539-3054T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663591 | ||||||
chr2:241663794
|
A | G | 3 | a0001c0002t0003g0188a0003c0004t0007g0193a0003c0004t0007g0195 | 3 | HG01515.hp1 HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.539-2851A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663794 | ||||||
chr2:241663811
|
A | AT | 76 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0315others(73): Show | 87 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.539-2818dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241663811 | |||||
chr2:241663811
|
A | ATT | 41 | a0001c0002t0003g0074a0001c0002t0003g0173a0001c0002t0005g0014others(38): Show | 43 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.539-2819_539-2818d others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241663811 | |||||
chr2:241663811
|
AT | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0219a0001c0001t0001g0254others(1): Show | 7 | HG01074.hp2 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.539-2818delT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241663811 | |||||
chr2:241663823
|
T | G | 13 | a0001c0001t0006g0007a0001c0001t0006g0144a0001c0001t0006g0147others(10): Show | 16 | HG01261.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-2822T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663823 | ||||||
chr2:241663829
|
G | C | 14 | a0001c0001t0006g0007a0001c0001t0006g0144a0001c0001t0006g0147others(11): Show | 17 | HG01261.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.539-2816G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663829 | ||||||
chr2:241663846
|
C | T | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539-2799C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663846 | ||||||
chr2:241663895
|
C | T | 1 | a0001c0002t0005g0073 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.539-2750C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663895 | ||||||
chr2:241663927
|
A | G | 1 | a0001c0001t0002g0291 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.539-2718A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241663927 | ||||||
chr2:241664025
|
G | A | 2 | a0001c0001t0002g0277a0001c0001t0002g0298 | 2 | NA18962.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.539-2620G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664025 | ||||||
chr2:241664039
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.539-2606T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664039 | ||||||
chr2:241664040
|
G | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0055 | 2 | HG01261.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.539-2605G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664040 | ||||||
chr2:241664138
|
A | G | 1 | a0001c0002t0003g0245 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.539-2507A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664138 | ||||||
chr2:241664164
|
T | G | 39 | a0001c0001t0001g0334a0001c0002t0003g0074a0001c0002t0005g0014others(36): Show | 41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.539-2481T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664164 | ||||||
chr2:241664255
|
A | G | 245 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0035others(242): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.539-2390A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664255 | ||||||
chr2:241664279
|
A | G | 3 | a0001c0001t0004g0143a0001c0001t0004g0154a0001c0001t0012g0155 | 3 | HG01099.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.539-2366A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664279 | ||||||
chr2:241664308
|
T | G | 83 | a0001c0001t0001g0233a0001c0001t0001g0254a0001c0001t0001g0288others(80): Show | 90 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.539-2337T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664308 | ||||||
chr2:241664318
|
C | G | 1 | a0001c0002t0003g0043 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.539-2327C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664318 | ||||||
chr2:241664394
|
C | T | 1 | a0001c0001t0006g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.539-2251C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664394 | ||||||
chr2:241664459
|
G | T | 3 | a0001c0002t0013g0068a0001c0002t0013g0079a0001c0002t0013g0089 | 3 | HG00597.hp1 HG00621.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.539-2186G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664459 | ||||||
chr2:241664471
|
G | A | 1 | a0002c0003t0043g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-2174G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664471 | ||||||
chr2:241664596
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.539-2049A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664596 | ||||||
chr2:241664601
|
C | T | 1 | a0001c0001t0009g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.539-2044C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664601 | ||||||
chr2:241664660
|
C | G | 99 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0012others(96): Show | 110 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.539-1985C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664660 | ||||||
chr2:241664729
|
T | C | 1 | a0001c0002t0003g0102 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.539-1916T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664729 | ||||||
chr2:241664754
|
A | G | 11 | a0001c0002t0003g0008a0001c0002t0003g0025a0001c0002t0003g0182others(8): Show | 14 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-1891A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664754 | ||||||
chr2:241664825
|
G | A | 167 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0012others(164): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.539-1820G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664825 | ||||||
chr2:241664912
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.539-1733C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664912 | ||||||
chr2:241664961
|
A | G | 47 | a0001c0001t0002g0263a0001c0001t0002g0265a0001c0001t0002g0269others(44): Show | 49 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.539-1684A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241664961 | ||||||
chr2:241665039
|
A | G | 45 | a0001c0001t0002g0303a0001c0002t0003g0008a0001c0002t0003g0018others(42): Show | 52 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.539-1606A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665039 | ||||||
chr2:241665366
|
C | T | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-1279C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665366 | ||||||
chr2:241665391
|
G | A | 14 | a0001c0001t0006g0007a0001c0001t0006g0141a0001c0001t0006g0144others(11): Show | 16 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-1254G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665391 | ||||||
chr2:241665466
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.539-1179T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665466 | ||||||
chr2:241665674
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(97): Show | 119 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.539-971G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665674 | ||||||
chr2:241665834
|
T | C | 1 | a0002c0003t0043g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-811T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665834 | ||||||
chr2:241665835
|
C | T | 1 | a0002c0003t0043g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.539-810C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665835 | ||||||
chr2:241665916
|
A | G | 5 | a0003c0004t0007g0026a0003c0004t0007g0194a0003c0004t0007g0196others(2): Show | 6 | HG02056.hp2 NA18959.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.539-729A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665916 | ||||||
chr2:241665947
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.539-698C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665947 | ||||||
chr2:241665947
|
C | G | 3 | a0002c0003t0014g0351a0002c0003t0014g0352a0002c0003t0014g0353 | 3 | HG00741.hp1 HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.539-698C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241665947 | ||||||
chr2:241666007
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(102): Show | 124 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.539-638G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666007 | ||||||
chr2:241666023
|
T | A | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.539-622T>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666023 | ||||||
chr2:241666109
|
C | T | 14 | a0001c0001t0006g0007a0001c0001t0006g0141a0001c0001t0006g0144others(11): Show | 16 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-536C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666109 | ||||||
chr2:241666136
|
C | T | 1 | a0001c0002t0015g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539-509C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666136 | ||||||
chr2:241666231
|
C | T | 92 | a0001c0001t0002g0253a0001c0002t0003g0008a0001c0002t0003g0018others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.539-414C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666231 | ||||||
chr2:241666260
|
C | T | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-385C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666260 | ||||||
chr2:241666261
|
G | A | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-384G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666261 | ||||||
chr2:241666282
|
G | T | 1 | a0001c0001t0020g0310 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.539-363G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666282 | ||||||
chr2:241666526
|
T | C | 1 | a0001c0002t0003g0146 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.539-119T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666526 | ||||||
chr2:241666527
|
G | A | 24 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0254others(21): Show | 26 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.539-118G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666527 | ||||||
chr2:241666539
|
C | T | 3 | a0001c0002t0003g0115a0001c0006t0003g0122a0001c0006t0003g0123 | 3 | HG01109.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.539-106C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666539 | ||||||
chr2:241666547
|
C | T | 91 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(88): Show | 100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.539-98C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666547 | ||||||
chr2:241666591
|
G | T | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-54G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666591 | ||||||
chr2:241666593
|
A | T | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.539-52A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666593 | ||||||
chr2:241666621
|
G | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(102): Show | 124 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.539-24G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 7/12 | chr2 | 241666621 | ||||||
chr2:241666913
|
G | A | 1 | a0001c0002t0003g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.732+75G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666913 | ||||||
chr2:241666916
|
G | A | 3 | a0001c0002t0005g0088a0001c0002t0022g0086a0001c0002t0022g0087 | 3 | HG00438.hp1 HG00673.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.732+78G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666916 | ||||||
chr2:241666925
|
C | T | 1 | a0006c0011t0007g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.732+87C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666925 | ||||||
chr2:241666946
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.732+108G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666946 | ||||||
chr2:241666976
|
C | T | 1 | a0001c0002t0025g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.732+138C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241666976 | ||||||
chr2:241667096
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(194): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.732+258T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667096 | ||||||
chr2:241667250
|
C | T | 14 | a0001c0001t0006g0007a0001c0001t0006g0141a0001c0001t0006g0144others(11): Show | 16 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.732+412C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667250 | ||||||
chr2:241667268
|
A | T | 1 | a0002c0003t0043g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.732+430A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667268 | ||||||
chr2:241667432
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(194): Show | 225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.732+594T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667432 | ||||||
chr2:241667450
|
A | G | 1 | a0001c0001t0017g0038 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.732+612A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667450 | ||||||
chr2:241667477
|
G | A | 1 | a0003c0004t0010g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.732+639G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667477 | ||||||
chr2:241667493
|
A | T | 1 | a0002c0003t0043g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.733-650A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667493 | ||||||
chr2:241667607
|
TA | T | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(6): Show | 9 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-521delA | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 241667607 | |||||
chr2:241667608
|
A | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(71): Show | 90 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.733-535A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667608 | ||||||
chr2:241667609
|
A | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-534A>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667609 | ||||||
chr2:241667683
|
C | T | 1 | a0001c0002t0003g0182 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.733-460C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667683 | ||||||
chr2:241667684
|
A | G | 21 | a0001c0002t0005g0016a0001c0002t0005g0071a0001c0002t0005g0072others(18): Show | 21 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.733-459A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667684 | ||||||
chr2:241667895
|
C | T | 21 | a0003c0004t0007g0026a0003c0004t0007g0190a0003c0004t0007g0191others(18): Show | 23 | HG01099.hp1 HG01515.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.733-248C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241667895 | ||||||
chr2:241668036
|
T | C | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.733-107T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241668036 | ||||||
chr2:241668068
|
G | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(102): Show | 124 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.733-75G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241668068 | ||||||
chr2:241668069
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(102): Show | 124 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.733-74C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241668069 | ||||||
chr2:241668091
|
G | C | 1 | a0001c0001t0001g0331 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.733-52G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 8/12 | chr2 | 241668091 | ||||||
chr2:241668348
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.811+127T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 9/12 | chr2 | 241668348 | ||||||
chr2:241668363
|
C | A | 4 | a0002c0003t0014g0202a0002c0003t0014g0351a0002c0003t0014g0352others(1): Show | 4 | HG00741.hp1 HG01071.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.811+142C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 9/12 | chr2 | 241668363 | ||||||
chr2:241668392
|
G | C | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.812-148G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 9/12 | chr2 | 241668392 | ||||||
chr2:241668509
|
A | G | 92 | a0001c0001t0002g0100a0001c0002t0003g0008a0001c0002t0003g0018others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.812-31A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 9/12 | chr2 | 241668509 | ||||||
chr2:241668700
|
C | G | 2 | a0001c0001t0002g0272a0001c0001t0002g0273 | 2 | HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.957+15C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668700 | ||||||
chr2:241668766
|
G | GC | 42 | a0001c0002t0005g0014a0001c0002t0005g0016a0001c0002t0005g0017others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.957+82dupC | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241668766 | |||||
chr2:241668768
|
G | GT | 53 | a0001c0001t0001g0327a0001c0001t0002g0292a0001c0001t0002g0297others(50): Show | 60 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.957+93dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241668768 | |||||
chr2:241668768
|
G | T | 42 | a0001c0002t0005g0014a0001c0002t0005g0016a0001c0002t0005g0017others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.957+83G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668768 | ||||||
chr2:241668777
|
T | C | 2 | a0001c0001t0009g0178a0001c0001t0009g0179 | 2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.957+92T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668777 | ||||||
chr2:241668789
|
G | C | 23 | a0001c0001t0004g0149a0001c0001t0006g0007a0001c0001t0006g0141others(20): Show | 28 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.957+104G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668789 | ||||||
chr2:241668872
|
C | T | 1 | a0001c0002t0005g0124 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.957+187C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668872 | ||||||
chr2:241668898
|
A | G | 1 | a0001c0001t0037g0293 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.957+213A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668898 | ||||||
chr2:241668941
|
G | A | 1 | a0001c0002t0003g0102 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.957+256G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668941 | ||||||
chr2:241668948
|
G | A | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.957+263G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241668948 | ||||||
chr2:241669018
|
CACACGGG others(48): Show |
C | 83 | a0001c0001t0001g0003a0001c0002t0003g0008a0001c0002t0003g0018others(80): Show | 95 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.957+359_957+413del others(55): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241669018 | |||||
chr2:241669022
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 118 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.957+337C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669022 | ||||||
chr2:241669069
|
T | C | 4 | a0001c0002t0003g0162a0001c0002t0003g0163a0001c0002t0003g0164others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+384T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669069 | ||||||
chr2:241669100
|
C | T | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.957+415C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669100 | ||||||
chr2:241669123
|
C | T | 1 | a0001c0002t0003g0184 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.957+438C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669123 | ||||||
chr2:241669124
|
G | A | 2 | a0001c0001t0037g0293a0003c0004t0010g0205 | 2 | HG00438.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.957+439G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669124 | ||||||
chr2:241669145
|
C | T | 1 | a0001c0001t0006g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.957+460C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669145 | ||||||
chr2:241669257
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0342 | 2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.957+572G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669257 | ||||||
chr2:241669299
|
G | A | 93 | a0001c0001t0001g0054a0001c0002t0003g0008a0001c0002t0003g0018others(90): Show | 102 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.957+614G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669299 | ||||||
chr2:241669351
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01081.hp2 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+666C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669351 | ||||||
chr2:241669414
|
G | A | 42 | a0001c0002t0005g0014a0001c0002t0005g0016a0001c0002t0005g0017others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.957+729G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669414 | ||||||
chr2:241669504
|
TTTTG | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(103): Show | 125 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.957+835_957+838del others(4): Show |
ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241669504 | |||||
chr2:241669546
|
C | T | 50 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(47): Show | 57 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.957+861C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669546 | ||||||
chr2:241669568
|
C | T | 23 | a0001c0001t0006g0007a0001c0001t0006g0141a0001c0001t0006g0144others(20): Show | 29 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.957+883C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669568 | ||||||
chr2:241669569
|
A | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(314): Show | 357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.957+884A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669569 | ||||||
chr2:241669622
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(100): Show | 121 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.957+937C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669622 | ||||||
chr2:241669632
|
G | C | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.957+947G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669632 | ||||||
chr2:241669663
|
A | C | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.957+978A>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669663 | ||||||
chr2:241669679
|
C | A | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.957+994C>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669679 | ||||||
chr2:241669728
|
T | C | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-998T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669728 | ||||||
chr2:241669743
|
A | G | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-983A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669743 | ||||||
chr2:241669801
|
G | A | 90 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(87): Show | 99 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.958-925G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669801 | ||||||
chr2:241669811
|
G | T | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.958-915G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669811 | ||||||
chr2:241669837
|
C | T | 1 | a0001c0001t0002g0251 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.958-889C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669837 | ||||||
chr2:241669850
|
G | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(217): Show | 254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.958-876G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669850 | ||||||
chr2:241669885
|
A | G | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-841A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669885 | ||||||
chr2:241669908
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(102): Show | 124 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.958-818G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669908 | ||||||
chr2:241669913
|
C | CT | 50 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(47): Show | 57 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.958-812dupT | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241669913 | |||||
chr2:241669946
|
C | T | 1 | a0001c0002t0005g0078 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.958-780C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241669946 | ||||||
chr2:241670021
|
C | T | 91 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(88): Show | 100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.958-705C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670021 | ||||||
chr2:241670089
|
T | C | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-637T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670089 | ||||||
chr2:241670139
|
C | T | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-587C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670139 | ||||||
chr2:241670140
|
G | A | 1 | a0001c0001t0004g0154 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.958-586G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670140 | ||||||
chr2:241670171
|
G | T | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.958-555G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670171 | ||||||
chr2:241670232
|
G | C | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-494G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670232 | ||||||
chr2:241670245
|
C | G | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-481C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670245 | ||||||
chr2:241670317
|
C | T | 1 | a0002c0003t0043g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.958-409C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670317 | ||||||
chr2:241670318
|
T | C | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.958-408T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670318 | ||||||
chr2:241670374
|
C | T | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-352C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670374 | ||||||
chr2:241670424
|
T | C | 1 | a0001c0001t0017g0038 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.958-302T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670424 | ||||||
chr2:241670435
|
C | T | 1 | a0001c0001t0002g0307 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.958-291C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670435 | ||||||
chr2:241670505
|
G | A | 1 | a0002c0003t0004g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.958-221G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670505 | ||||||
chr2:241670572
|
G | A | 50 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(47): Show | 57 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.958-154G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670572 | ||||||
chr2:241670577
|
T | C | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.958-149T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670577 | ||||||
chr2:241670604
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.958-122A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 10/12 | chr2 | 241670604 | ||||||
chr2:241670838
|
T | C | 98 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(95): Show | 107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1014+56T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241670838 | ||||||
chr2:241670925
|
T | C | 1 | a0001c0001t0006g0141 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1014+143T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241670925 | ||||||
chr2:241670990
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(103): Show | 125 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.1014+208C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241670990 | ||||||
chr2:241671002
|
G | A | 22 | a0001c0001t0006g0007a0001c0001t0006g0141a0001c0001t0006g0144others(19): Show | 27 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1014+220G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671002 | ||||||
chr2:241671087
|
G | A | 3 | a0001c0001t0016g0159a0001c0001t0016g0160a0001c0001t0016g0161 | 3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1015-225G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671087 | ||||||
chr2:241671087
|
G | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(195): Show | 226 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1015-225G>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671087 | ||||||
chr2:241671092
|
C | T | 1 | a0001c0002t0005g0170 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1015-220C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671092 | ||||||
chr2:241671225
|
C | T | 42 | a0001c0002t0005g0014a0001c0002t0005g0016a0001c0002t0005g0017others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1015-87C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671225 | ||||||
chr2:241671266
|
A | G | 3 | a0001c0001t0016g0159a0001c0001t0016g0160a0001c0001t0016g0161 | 3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1015-46A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 11/12 | chr2 | 241671266 | ||||||
chr2:241671452
|
T | C | 1 | a0001c0002t0003g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1108+47T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671452 | ||||||
chr2:241671464
|
C | T | 4 | a0002c0003t0014g0202a0002c0003t0014g0351a0002c0003t0014g0352others(1): Show | 4 | HG00741.hp1 HG01071.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108+59C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671464 | ||||||
chr2:241671635
|
C | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(102): Show | 124 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1108+230C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671635 | ||||||
chr2:241671640
|
G | A | 22 | a0001c0001t0006g0007a0001c0001t0006g0141a0001c0001t0006g0144others(19): Show | 27 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1108+235G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671640 | ||||||
chr2:241671655
|
G | A | 3 | a0003c0004t0010g0205a0003c0004t0010g0206a0003c0004t0034g0208 | 3 | HG02647.hp1 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1108+250G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671655 | ||||||
chr2:241671752
|
C | G | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1108+347C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671752 | ||||||
chr2:241671762
|
G | C | 1 | a0003c0004t0034g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1108+357G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671762 | ||||||
chr2:241671817
|
G | A | 1 | a0001c0001t0018g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1109-374G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671817 | ||||||
chr2:241671842
|
C | T | 1 | a0001c0001t0002g0253 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1109-349C>T | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671842 | ||||||
chr2:241671857
|
T | C | 92 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(89): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1109-334T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671857 | ||||||
chr2:241671872
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(102): Show | 124 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1109-319G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671872 | ||||||
chr2:241671911
|
T | G | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0342 | 3 | HG02451.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1109-280T>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671911 | ||||||
chr2:241671934
|
G | C | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1109-257G>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671934 | ||||||
chr2:241671959
|
A | G | 42 | a0001c0002t0005g0014a0001c0002t0005g0016a0001c0002t0005g0017others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1109-232A>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671959 | ||||||
chr2:241671963
|
T | C | 1 | a0001c0002t0003g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1109-228T>C | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671963 | ||||||
chr2:241671994
|
C | G | 2 | a0003c0008t0019g0041a0003c0008t0019g0042 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1109-197C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241671994 | ||||||
chr2:241672132
|
G | A | 90 | a0001c0002t0003g0008a0001c0002t0003g0018a0001c0002t0003g0019others(87): Show | 98 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1109-59G>A | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241672132 | ||||||
chr2:241672136
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1109-55C>G | ATG4B | ENSG00000168397.17 | transcript | ENST00000404914.8 | protein_coding | 12/12 | chr2 | 241672136 |