geneid | 2028 |
---|---|
ensemblid | ENSG00000138792.10 |
hgncid | 3355 |
symbol | ENPEP |
name | glutamyl aminopeptidase |
refseq_nuc | NM_001977.4 |
refseq_prot | NP_001968.3 |
ensembl_nuc | ENST00000265162.10 |
ensembl_prot | ENSP00000265162.5 |
mane_status | MANE Select |
chr | chr4 |
start | 110476155 |
end | 110565285 |
strand | + |
ver | v1.2 |
region | chr4:110476155-110565285 |
region5000 | chr4:110471155-110570285 |
regionname0 | ENPEP_chr4_110476155_110565285 |
regionname5000 | ENPEP_chr4_110471155_110570285 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 957 | 153 | 32 | 20 | 73 | 8 | 20 | 52 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002 | 0/1 | 957 | 87 | 24 | 23 | 25 | 3 | 11 | 16 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003 | 1/0 | 957 | 42 | 11 | 6 | 17 | 1 | 6 | 12 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0004 | 0/0 | 957 | 10 | 0 | 0 | 9 | 0 | 1 | 7 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0005 | 0/0 | 957 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0006 | 0/0 | 957 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0007 | 0/0 | 957 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0008 | 0/0 | 957 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0009 | 0/0 | 957 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0010 | 0/0 | 957 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0011 | 0/0 | 957 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0012 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0013 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0014 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0015 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0016 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0017 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2874 | 150 | 29 | 20 | 73 | 8 | 20 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0002 | 0/1 | 2874 | 85 | 24 | 22 | 25 | 2 | 11 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0003 | 1/0 | 2874 | 41 | 10 | 6 | 17 | 1 | 6 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0004 | 0/0 | 2874 | 10 | 0 | 0 | 9 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0005 | 0/0 | 2874 | 6 | 6 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0006 | 0/0 | 2874 | 2 | 0 | 1 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0007 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0008 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0009 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0010 | 0/0 | 2874 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0011 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0012 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0013 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0014 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0015 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0016 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0017 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0018 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0019 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0020 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0021 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
c0022 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3988 | 131 | 26 | 26 | 59 | 8 | 12 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0002 | 0/0 | 3988 | 67 | 10 | 8 | 35 | 0 | 14 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0003 | 1/1 | 3988 | 28 | 6 | 2 | 11 | 1 | 6 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0004 | 0/0 | 3988 | 17 | 6 | 5 | 3 | 0 | 3 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0005 | 0/0 | 3988 | 17 | 17 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0006 | 0/0 | 3988 | 10 | 0 | 0 | 9 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0007 | 0/0 | 3988 | 8 | 7 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0008 | 0/0 | 3988 | 3 | 0 | 2 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0009 | 0/0 | 3988 | 3 | 1 | 1 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0010 | 0/0 | 3988 | 2 | 0 | 2 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0011 | 0/0 | 3988 | 2 | 1 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0012 | 0/0 | 3988 | 2 | 0 | 0 | 0 | 1 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0013 | 0/0 | 3988 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0014 | 0/0 | 3988 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0015 | 0/0 | 3988 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0016 | 0/0 | 3988 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0017 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0018 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0019 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0020 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0021 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0022 | 0/0 | 3988 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0023 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0024 | 0/0 | 3988 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0025 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0026 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0027 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0028 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0029 | 0/0 | 3988 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
t0030 | 0/0 | 3988 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0003 | 0/1 | 3 | 0 | 0 | 0 | 1 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2874 | 150 | 29 | 20 | 73 | 8 | 20 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0007 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0014 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002 | 0/1 | 2874 | 85 | 24 | 22 | 25 | 2 | 11 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0006 | 0/0 | 2874 | 2 | 0 | 1 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0003 | 1/0 | 2874 | 41 | 10 | 6 | 17 | 1 | 6 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0012 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0004c0004 | 0/0 | 2874 | 10 | 0 | 0 | 9 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0005c0005 | 0/0 | 2874 | 6 | 6 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0006c0008 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0006c0021 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0007c0010 | 0/0 | 2874 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0008c0020 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0009c0013 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0010c0016 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0011c0015 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0012c0009 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0013c0019 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0014c0018 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0015c0017 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0016c0011 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0017c0022 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6861 | 74 | 15 | 10 | 34 | 7 | 8 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0002 | 0/0 | 6861 | 32 | 4 | 4 | 20 | 0 | 4 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0003 | 0/0 | 6861 | 6 | 1 | 0 | 3 | 0 | 2 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0004 | 0/0 | 6861 | 6 | 0 | 2 | 2 | 0 | 2 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0005 | 0/0 | 6861 | 4 | 4 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0006 | 0/0 | 6861 | 9 | 0 | 0 | 8 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0007 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0008 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0009 | 0/0 | 6861 | 3 | 1 | 1 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0011 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0012 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0014 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0015 | 0/0 | 6861 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0017 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0018 | 0/0 | 6734 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0019 | 0/0 | 6861 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0020 | 0/0 | 6861 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0022 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0026 | 0/0 | 6861 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0027 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0028 | 0/0 | 6861 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0001t0030 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0007t0001 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0007t0003 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0001c0014t0029 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0001 | 0/0 | 6861 | 37 | 3 | 14 | 17 | 1 | 2 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0002 | 0/0 | 6861 | 14 | 1 | 3 | 5 | 0 | 5 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0003 | 0/1 | 6861 | 8 | 3 | 0 | 0 | 1 | 3 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0004 | 0/0 | 6861 | 6 | 3 | 1 | 1 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0005 | 0/0 | 6861 | 12 | 12 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0007 | 0/0 | 6861 | 2 | 1 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0008 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0010 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0014 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0016 | 0/0 | 6861 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0002t0025 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0006t0001 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0002c0006t0012 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0003t0001 | 0/0 | 6861 | 9 | 3 | 0 | 6 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0003t0002 | 0/0 | 6861 | 13 | 4 | 1 | 3 | 0 | 5 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0003t0003 | 1/0 | 6861 | 11 | 0 | 2 | 8 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0003t0004 | 0/0 | 6861 | 4 | 2 | 2 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0003t0007 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0003t0008 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0003t0010 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0003t0024 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0003c0012t0003 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0004c0004t0001 | 0/0 | 6861 | 3 | 0 | 0 | 2 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0004c0004t0002 | 0/0 | 6861 | 7 | 0 | 0 | 7 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0005c0005t0001 | 0/0 | 6861 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0005c0005t0007 | 0/0 | 6861 | 4 | 4 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0006c0008t0004 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0006c0008t0021 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0006c0021t0001 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0007c0010t0001 | 0/0 | 6861 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0008c0020t0023 | 0/0 | 6861 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0009c0013t0001 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0010c0016t0006 | 0/0 | 6861 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0011c0015t0003 | 0/0 | 6861 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0012c0009t0013 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0013c0019t0011 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0014c0018t0013 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0015c0017t0002 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0016c0011t0005 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
a0017c0022t0001 | 0/0 | 6861 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | copy fasta | chr4 | 110471155 | 110570285 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0006g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0008g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0009g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0011g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0014g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0015g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0015g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0017g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0018g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0019g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0020g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0022g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0026g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0027g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0028g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0001t0030g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0007t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0007t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0001c0014t0029g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0003g0003 | 0/1 | 3 | 0 | 0 | 0 | 1 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0008g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0010g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0014g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0016g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0002t0025g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0006t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0002c0006t0012g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0003g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0008g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0010g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0003t0024g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0003c0012t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0004c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0004c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0004c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0004c0004t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0004c0004t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0004c0004t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0004c0004t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0005c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0005c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0005c0005t0007g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0005c0005t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0005c0005t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0006c0008t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0006c0008t0021g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0006c0021t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0007c0010t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0008c0020t0023g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0009c0013t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0010c0016t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0011c0015t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0012c0009t0013g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0013c0019t0011g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0014c0018t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0015c0017t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0016c0011t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
a0017c0022t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0001 | g0222 | EUR | GBR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | GBR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00280 | hp1 | a0002 | c0006 | t0012 | g0028 | EUR | FIN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00280 | hp2 | a0001 | c0001 | t0009 | g0007 | EUR | FIN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0257 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00423 | hp2 | a0003 | c0003 | t0003 | g0283 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00438 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00597 | hp1 | a0001 | c0001 | t0028 | g0184 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00642 | hp1 | a0002 | c0002 | t0004 | g0034 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00673 | hp1 | a0004 | c0004 | t0002 | g0020 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00673 | hp2 | a0003 | c0003 | t0001 | g0242 | EAS | CHS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00735 | hp1 | a0002 | c0002 | t0007 | g0099 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00741 | hp1 | a0003 | c0003 | t0004 | g0273 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0189 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01074 | hp1 | a0002 | c0002 | t0010 | g0036 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01175 | hp1 | a0003 | c0003 | t0010 | g0237 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01243 | hp1 | a0001 | c0001 | t0011 | g0068 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0168 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0128 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01256 | hp1 | a0003 | c0003 | t0003 | g0015 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01256 | hp2 | a0002 | c0006 | t0001 | g0029 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01258 | hp2 | a0003 | c0003 | t0003 | g0015 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01261 | hp1 | a0001 | c0001 | t0030 | g0193 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01261 | hp2 | a0002 | c0002 | t0025 | g0244 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0251 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01361 | hp1 | a0001 | c0001 | t0008 | g0065 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01361 | hp2 | a0003 | c0003 | t0004 | g0246 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0255 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0003 | EUR | IBS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01891 | hp1 | a0001 | c0014 | t0029 | g0074 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01891 | hp2 | a0017 | c0022 | t0001 | g0158 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01928 | hp2 | a0007 | c0010 | t0001 | g0216 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01934 | hp2 | a0002 | c0002 | t0008 | g0037 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01975 | hp2 | a0003 | c0003 | t0002 | g0279 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0241 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02040 | hp2 | a0004 | c0004 | t0002 | g0019 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02055 | hp1 | a0003 | c0003 | t0001 | g0236 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02055 | hp2 | a0012 | c0009 | t0013 | g0224 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02080 | hp2 | a0008 | c0020 | t0023 | g0232 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02132 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02145 | hp1 | a0002 | c0002 | t0004 | g0041 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02145 | hp2 | a0003 | c0003 | t0001 | g0275 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CDX | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | CDX | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02257 | hp1 | a0003 | c0003 | t0002 | g0282 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0180 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0031 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02280 | hp1 | a0002 | c0002 | t0007 | g0109 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02280 | hp2 | a0002 | c0002 | t0005 | g0026 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0239 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02451 | hp2 | a0002 | c0002 | t0005 | g0040 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02572 | hp1 | a0015 | c0017 | t0002 | g0229 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0148 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02622 | hp1 | a0001 | c0007 | t0001 | g0143 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0067 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02647 | hp1 | a0002 | c0002 | t0005 | g0044 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02647 | hp2 | a0003 | c0003 | t0002 | g0021 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0103 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02717 | hp2 | a0002 | c0002 | t0005 | g0045 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0179 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02723 | hp2 | a0006 | c0021 | t0001 | g0167 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02735 | hp1 | a0003 | c0003 | t0002 | g0260 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02735 | hp2 | a0003 | c0003 | t0002 | g0238 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0032 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02738 | hp2 | a0001 | c0001 | t0022 | g0124 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02809 | hp1 | a0001 | c0001 | t0027 | g0142 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02809 | hp2 | a0002 | c0002 | t0003 | g0054 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02896 | hp1 | a0005 | c0005 | t0007 | g0011 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02897 | hp1 | a0005 | c0005 | t0007 | g0011 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02922 | hp2 | a0002 | c0002 | t0003 | g0023 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02965 | hp1 | a0002 | c0002 | t0005 | g0050 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02965 | hp2 | a0003 | c0003 | t0004 | g0281 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02970 | hp2 | a0014 | c0018 | t0013 | g0042 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0272 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03017 | hp2 | a0009 | c0013 | t0001 | g0265 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03098 | hp1 | a0005 | c0005 | t0007 | g0155 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03139 | hp1 | a0002 | c0002 | t0005 | g0039 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03195 | hp1 | a0002 | c0002 | t0005 | g0049 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03225 | hp1 | a0001 | c0001 | t0014 | g0230 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03225 | hp2 | a0002 | c0002 | t0005 | g0108 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03239 | hp1 | a0004 | c0004 | t0001 | g0233 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03239 | hp2 | a0011 | c0015 | t0003 | g0190 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03453 | hp1 | a0002 | c0002 | t0004 | g0027 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03453 | hp2 | a0016 | c0011 | t0005 | g0277 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03486 | hp1 | a0003 | c0003 | t0007 | g0280 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03516 | hp1 | a0002 | c0002 | t0005 | g0051 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0101 | AFR | ESN | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03540 | hp1 | a0005 | c0005 | t0007 | g0154 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03540 | hp2 | a0003 | c0003 | t0002 | g0021 | AFR | GWD | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03579 | hp1 | a0006 | c0008 | t0004 | g0157 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03579 | hp2 | a0003 | c0003 | t0002 | g0235 | AFR | MSL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03669 | hp2 | a0002 | c0002 | t0003 | g0003 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03688 | hp1 | a0001 | c0001 | t0018 | g0072 | SAS | STU | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | STU | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0152 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03710 | hp2 | a0002 | c0002 | t0003 | g0058 | SAS | PJL | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0127 | SAS | BEB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03834 | hp2 | a0003 | c0003 | t0002 | g0262 | SAS | BEB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0033 | SAS | BEB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG03927 | hp2 | a0003 | c0003 | t0002 | g0250 | SAS | BEB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG04115 | hp2 | a0002 | c0002 | t0003 | g0030 | SAS | STU | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG04184 | hp1 | a0001 | c0001 | t0012 | g0151 | SAS | BEB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0094 | SAS | BEB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG04199 | hp1 | a0003 | c0003 | t0002 | g0256 | SAS | STU | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0082 | SAS | STU | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG04228 | hp1 | a0003 | c0003 | t0024 | g0249 | SAS | STU | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | CHB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CHB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18747 | hp2 | a0002 | c0002 | t0004 | g0169 | EAS | CHB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18906 | hp2 | a0002 | c0002 | t0005 | g0107 | AFR | YRI | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18941 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18942 | hp1 | a0003 | c0003 | t0002 | g0258 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18946 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18948 | hp1 | a0003 | c0003 | t0003 | g0247 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18949 | hp2 | a0004 | c0004 | t0001 | g0268 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18950 | hp2 | a0004 | c0004 | t0001 | g0269 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18959 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18968 | hp2 | a0001 | c0001 | t0019 | g0060 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18969 | hp1 | a0004 | c0004 | t0002 | g0270 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18970 | hp1 | a0001 | c0001 | t0026 | g0123 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18971 | hp1 | a0004 | c0004 | t0002 | g0267 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18971 | hp2 | a0001 | c0001 | t0015 | g0059 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18974 | hp2 | a0001 | c0001 | t0020 | g0178 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18980 | hp1 | a0001 | c0001 | t0015 | g0110 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18989 | hp1 | a0010 | c0016 | t0006 | g0129 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18991 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18995 | hp2 | a0003 | c0003 | t0002 | g0263 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19000 | hp2 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19001 | hp1 | a0001 | c0001 | t0006 | g0075 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19001 | hp2 | a0003 | c0003 | t0001 | g0276 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19004 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19004 | hp2 | a0004 | c0004 | t0002 | g0271 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19007 | hp2 | a0004 | c0004 | t0002 | g0019 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19009 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19011 | hp2 | a0003 | c0003 | t0003 | g0245 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19030 | hp1 | a0005 | c0005 | t0001 | g0159 | AFR | LWK | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19030 | hp2 | a0013 | c0019 | t0011 | g0285 | AFR | LWK | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19043 | hp1 | a0002 | c0002 | t0014 | g0100 | AFR | LWK | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19043 | hp2 | a0002 | c0002 | t0004 | g0083 | AFR | LWK | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19057 | hp1 | a0002 | c0002 | t0016 | g0009 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19057 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19066 | hp2 | a0003 | c0003 | t0002 | g0252 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19068 | hp2 | a0004 | c0004 | t0002 | g0020 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19072 | hp1 | a0003 | c0003 | t0003 | g0248 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19079 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19086 | hp1 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19088 | hp1 | a0002 | c0002 | t0016 | g0009 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20805 | hp2 | a0003 | c0003 | t0008 | g0254 | EUR | TSI | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20905 | hp1 | a0002 | c0002 | t0004 | g0035 | SAS | GIH | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | GIH | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02109 | hp1 | a0001 | c0007 | t0003 | g0022 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02109 | hp2 | a0003 | c0003 | t0004 | g0274 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02486 | hp1 | a0002 | c0002 | t0005 | g0043 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02486 | hp2 | a0005 | c0005 | t0001 | g0153 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG02559 | hp2 | a0002 | c0002 | t0005 | g0098 | AFR | ACB | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG06807 | hp1 | a0006 | c0008 | t0021 | g0156 | AFR | USA | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
HG06807 | hp2 | a0003 | c0012 | t0003 | g0278 | AFR | USA | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18955 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20300 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | USA | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA20300 | hp2 | a0001 | c0001 | t0017 | g0192 | AFR | USA | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | LWK | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | LWK | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0003 | g0003 | REF | REF | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0003 | g0240 | REF | REF | ENPEP_chr4_110471155_110570285 | ENPEP | chr4 | 110471155 | 110570285 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:110476508
|
A | G | 3 | a0005a0006a0017 | 10 | HG01891.hp2 HG02486.hp2 HG02723.hp2 others(7): Show |
missense_variant | MODERATE | c.94A>G | p.Ile32Val | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/20 | 354/6861 | 94/2874 | 32/957 | chr4 | 110476508 | ||
chr4:110476703
|
G | A | 1 | a0007 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.289G>A | p.Val97Ile | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/20 | 549/6861 | 289/2874 | 97/957 | chr4 | 110476703 | ||
chr4:110476848
|
C | T | 1 | a0008 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.434C>T | p.Pro145Leu | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/20 | 694/6861 | 434/2874 | 145/957 | chr4 | 110476848 | ||
chr4:110476928
|
G | C | 1 | a0016 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.514G>C | p.Glu172Gln | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/20 | 774/6861 | 514/2874 | 172/957 | chr4 | 110476928 | ||
chr4:110477052
|
A | G | 13 | a0001a0002a0005others(10): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
missense_variant | MODERATE | c.638A>G | p.Gln213Arg | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/20 | 898/6861 | 638/2874 | 213/957 | chr4 | 110477052 | ||
chr4:110488549
|
T | C | 7 | a0001a0004a0006others(4): Show | 170 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(167): Show |
missense_variant | MODERATE | c.653T>C | p.Val218Ala | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/20 | 913/6861 | 653/2874 | 218/957 | chr4 | 110488549 | ||
chr4:110491097
|
C | T | 1 | a0010 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.851C>T | p.Thr284Met | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/20 | 1111/6861 | 851/2874 | 284/957 | chr4 | 110491097 | ||
chr4:110513415
|
C | A | 1 | a0015 | 1 | HG02572.hp1 | missense_variant&splice_region_variant | MODERATE | c.1309C>A | p.Arg437Ser | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/20 | 1569/6861 | 1309/2874 | 437/957 | chr4 | 110513415 | ||
chr4:110520270
|
A | T | 2 | a0013a0017 | 2 | HG01891.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.1631A>T | p.Tyr544Phe | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/20 | 1891/6861 | 1631/2874 | 544/957 | chr4 | 110520270 | ||
chr4:110520314
|
C | T | 1 | a0011 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1675C>T | p.Arg559Cys | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/20 | 1935/6861 | 1675/2874 | 559/957 | chr4 | 110520314 | ||
chr4:110542808
|
A | G | 1 | a0009 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1865A>G | p.Asp622Gly | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 12/20 | 2125/6861 | 1865/2874 | 622/957 | chr4 | 110542808 | ||
chr4:110553396
|
C | A | 2 | a0012a0014 | 2 | HG02055.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.2583C>A | p.Ser861Arg | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/20 | 2843/6861 | 2583/2874 | 861/957 | chr4 | 110553396 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:110476429
|
G | A | 1 | a0002c0006 | 2 | HG00280.hp1 HG01256.hp2 |
synonymous_variant | LOW | c.15G>A | p.Glu5Glu | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/20 | 275/6861 | 15/2874 | 5/957 | chr4 | 110476429 | ||
chr4:110476435
|
G | A | 1 | a0012c0009 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.21G>A | p.Glu7Glu | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/20 | 281/6861 | 21/2874 | 7/957 | chr4 | 110476435 | ||
chr4:110476522
|
C | T | 4 | a0005c0005a0006c0008a0006c0021others(1): Show | 10 | HG01891.hp2 HG02486.hp2 HG02723.hp2 others(7): Show |
synonymous_variant | LOW | c.108C>T | p.Ala36Ala | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/20 | 368/6861 | 108/2874 | 36/957 | chr4 | 110476522 | ||
chr4:110491134
|
T | C | 1 | a0001c0014 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.888T>C | p.Ser296Ser | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/20 | 1148/6861 | 888/2874 | 296/957 | chr4 | 110491134 | ||
chr4:110509807
|
G | A | 2 | a0001c0007a0006c0021 | 3 | HG02109.hp1 HG02622.hp1 HG02723.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1194G>A | p.Gln398Gln | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 5/20 | 1454/6861 | 1194/2874 | 398/957 | chr4 | 110509807 | ||
chr4:110515382
|
T | C | 1 | a0003c0012 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1449T>C | p.Ser483Ser | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/20 | 1709/6861 | 1449/2874 | 483/957 | chr4 | 110515382 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:110476240
|
G | A | 1 | a0001c0001t0017 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-175G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/20 | 175 | chr4 | 110476240 | |||||
chr4:110561561
|
T | A | 3 | a0001c0001t0008a0002c0002t0008a0003c0003t0008 | 3 | HG01361.hp1 HG01934.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 3 | chr4 | 110561561 | |||||
chr4:110561664
|
A | G | 1 | a0001c0001t0030 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*106A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 106 | chr4 | 110561664 | |||||
chr4:110561847
|
A | G | 1 | a0001c0001t0009 | 3 | HG00280.hp2 HG01496.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*289A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 289 | chr4 | 110561847 | |||||
chr4:110561977
|
C | A | 7 | a0001c0001t0004a0001c0001t0006a0001c0001t0018others(4): Show | 28 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*419C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 419 | chr4 | 110561977 | |||||
chr4:110562018
|
T | C | 1 | a0001c0001t0019 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*460T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 460 | chr4 | 110562018 | |||||
chr4:110562295
|
T | C | 2 | a0001c0001t0006a0010c0016t0006 | 10 | HG02698.hp2 NA18941.hp1 NA18946.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*737T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 737 | chr4 | 110562295 | |||||
chr4:110562297
|
C | G | 9 | a0001c0001t0002a0001c0001t0015a0001c0001t0028others(6): Show | 73 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*739C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 739 | chr4 | 110562297 | |||||
chr4:110562413
|
A | G | 13 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(10): Show | 48 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*855A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 855 | chr4 | 110562413 | |||||
chr4:110562889
|
AAAACCTT others(120): Show |
A | 1 | a0001c0001t0018 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1335_*1461del | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 1335 | INFO_REALIGN_3_PRIME | chr4 | 110562889 | ||||
chr4:110562983
|
A | G | 1 | a0002c0002t0016 | 2 | NA19057.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1425A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 1425 | chr4 | 110562983 | |||||
chr4:110562987
|
C | T | 30 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(27): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*1429C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 1429 | chr4 | 110562987 | |||||
chr4:110563427
|
A | G | 1 | a0006c0008t0021 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1869A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 1869 | chr4 | 110563427 | |||||
chr4:110563433
|
C | T | 2 | a0012c0009t0013a0014c0018t0013 | 2 | HG02055.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1875C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 1875 | chr4 | 110563433 | |||||
chr4:110563502
|
C | T | 1 | a0001c0001t0026 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1944C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 1944 | chr4 | 110563502 | |||||
chr4:110563579
|
C | T | 2 | a0001c0001t0014a0002c0002t0014 | 2 | HG03225.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2021C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 2021 | chr4 | 110563579 | |||||
chr4:110563611
|
T | C | 1 | a0001c0001t0022 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2053T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 2053 | chr4 | 110563611 | |||||
chr4:110563874
|
G | C | 1 | a0001c0001t0015 | 2 | NA18971.hp2 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2316G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 2316 | chr4 | 110563874 | |||||
chr4:110563932
|
T | A | 1 | a0008c0020t0023 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2374T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 2374 | chr4 | 110563932 | |||||
chr4:110564015
|
T | G | 10 | a0001c0001t0004a0001c0001t0006a0001c0001t0018others(7): Show | 31 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2457T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 2457 | chr4 | 110564015 | |||||
chr4:110564133
|
A | G | 1 | a0002c0002t0025 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2575A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 2575 | chr4 | 110564133 | |||||
chr4:110564205
|
T | G | 5 | a0001c0001t0005a0001c0001t0014a0002c0002t0005others(2): Show | 19 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2647T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 2647 | chr4 | 110564205 | |||||
chr4:110564713
|
T | C | 2 | a0001c0001t0011a0013c0019t0011 | 2 | HG01243.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3155T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 3155 | chr4 | 110564713 | |||||
chr4:110564838
|
C | T | 9 | a0001c0001t0002a0001c0001t0012a0001c0001t0015others(6): Show | 73 | HG00280.hp1 HG00544.hp2 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*3280C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 3280 | chr4 | 110564838 | |||||
chr4:110565006
|
T | C | 22 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(19): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*3448T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 3448 | chr4 | 110565006 | |||||
chr4:110565162
|
A | T | 1 | a0001c0001t0020 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3604A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 20/20 | 3604 | chr4 | 110565162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:110477096
|
C | A | 37 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0053others(34): Show | 42 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.644+38C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110477096 | ||||||
chr4:110477434
|
C | G | 1 | a0013c0019t0011g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.644+376C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110477434 | ||||||
chr4:110477637
|
C | T | 1 | a0001c0001t0007g0284 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.644+579C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110477637 | ||||||
chr4:110477684
|
T | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(17): Show | 21 | HG00735.hp2 HG01243.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.644+626T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110477684 | ||||||
chr4:110477684
|
T | G | 1 | a0001c0014t0029g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.644+626T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110477684 | ||||||
chr4:110477782
|
T | C | 75 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0001g0111others(72): Show | 80 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.644+724T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110477782 | ||||||
chr4:110477963
|
G | A | 225 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(222): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.644+905G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110477963 | ||||||
chr4:110478052
|
T | A | 1 | a0008c0020t0023g0232 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.644+994T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110478052 | ||||||
chr4:110478071
|
C | T | 1 | a0003c0003t0003g0283 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.644+1013C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110478071 | ||||||
chr4:110478308
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230others(1): Show | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+1250C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110478308 | ||||||
chr4:110478438
|
TA | T | 232 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(229): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.644+1384delA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 110478438 | |||||
chr4:110478442
|
A | G | 232 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(229): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.644+1384A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110478442 | ||||||
chr4:110478548
|
C | T | 1 | a0003c0003t0001g0276 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.644+1490C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110478548 | ||||||
chr4:110478587
|
T | C | 1 | a0001c0001t0002g0146 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.644+1529T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110478587 | ||||||
chr4:110478650
|
G | T | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.644+1592G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110478650 | ||||||
chr4:110478817
|
G | A | 1 | a0001c0007t0003g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.644+1759G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110478817 | ||||||
chr4:110479196
|
C | T | 7 | a0003c0003t0001g0275a0003c0003t0002g0021a0003c0003t0002g0279others(4): Show | 8 | HG01975.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.644+2138C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110479196 | ||||||
chr4:110479259
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.644+2201C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110479259 | ||||||
chr4:110479469
|
T | C | 75 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0001g0111others(72): Show | 80 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.644+2411T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110479469 | ||||||
chr4:110479470
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0006g0075 | 2 | NA18965.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.644+2412G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110479470 | ||||||
chr4:110479508
|
A | T | 4 | a0001c0001t0002g0144a0001c0001t0005g0145a0001c0001t0027g0142others(1): Show | 4 | HG02622.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+2450A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110479508 | ||||||
chr4:110479604
|
G | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0116a0001c0001t0001g0117others(32): Show | 39 | HG00621.hp1 HG01255.hp2 HG01516.hp2 others(36): Show |
intron_variant | MODIFIER | c.644+2546G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110479604 | ||||||
chr4:110479665
|
G | A | 5 | a0003c0003t0002g0021a0003c0003t0002g0279a0003c0003t0004g0281others(2): Show | 6 | HG01975.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.644+2607G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110479665 | ||||||
chr4:110479813
|
A | G | 7 | a0003c0003t0002g0021a0003c0003t0002g0279a0003c0003t0002g0282others(4): Show | 8 | HG01975.hp2 HG02257.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.644+2755A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110479813 | ||||||
chr4:110479916
|
T | C | 5 | a0003c0003t0002g0021a0003c0003t0002g0279a0003c0003t0004g0281others(2): Show | 6 | HG01975.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.644+2858T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110479916 | ||||||
chr4:110480041
|
G | C | 1 | a0002c0002t0003g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.644+2983G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110480041 | ||||||
chr4:110480065
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG03492.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.644+3007C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110480065 | ||||||
chr4:110480135
|
A | G | 2 | a0003c0003t0004g0281a0003c0003t0007g0280 | 2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.644+3077A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110480135 | ||||||
chr4:110480420
|
G | A | 1 | a0001c0001t0003g0077 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.644+3362G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110480420 | ||||||
chr4:110480795
|
G | A | 7 | a0001c0001t0002g0004a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 9 | HG00544.hp2 HG02056.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.644+3737G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110480795 | ||||||
chr4:110480826
|
C | T | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.644+3768C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110480826 | ||||||
chr4:110480827
|
G | A | 6 | a0005c0005t0001g0153a0005c0005t0007g0011a0005c0005t0007g0154others(3): Show | 7 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.644+3769G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110480827 | ||||||
chr4:110481448
|
T | G | 2 | a0005c0005t0001g0159a0017c0022t0001g0158 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.644+4390T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110481448 | ||||||
chr4:110481542
|
A | T | 2 | a0003c0003t0002g0282a0016c0011t0005g0277 | 2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.644+4484A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110481542 | ||||||
chr4:110481573
|
C | T | 1 | a0002c0002t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.644+4515C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110481573 | ||||||
chr4:110481604
|
C | T | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.644+4546C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110481604 | ||||||
chr4:110481845
|
G | GGT | 45 | a0001c0001t0001g0014a0001c0001t0001g0047a0001c0001t0001g0052others(42): Show | 52 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.644+4790_644+4791d others(4): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 110481845 | |||||
chr4:110482035
|
G | T | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.644+4977G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482035 | ||||||
chr4:110482046
|
C | T | 1 | a0002c0002t0003g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.644+4988C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482046 | ||||||
chr4:110482115
|
A | G | 39 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0053others(36): Show | 44 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.644+5057A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482115 | ||||||
chr4:110482146
|
C | A | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.644+5088C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482146 | ||||||
chr4:110482154
|
A | G | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.644+5096A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482154 | ||||||
chr4:110482211
|
C | A | 83 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0001g0111others(80): Show | 89 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.644+5153C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482211 | ||||||
chr4:110482244
|
A | G | 1 | a0017c0022t0001g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.644+5186A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482244 | ||||||
chr4:110482381
|
C | T | 2 | a0002c0002t0001g0222a0002c0002t0001g0223 | 2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.644+5323C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482381 | ||||||
chr4:110482442
|
T | C | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.644+5384T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482442 | ||||||
chr4:110482445
|
G | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.644+5387G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482445 | ||||||
chr4:110482638
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.644+5580G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482638 | ||||||
chr4:110482838
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.645-5703G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482838 | ||||||
chr4:110482918
|
A | G | 1 | a0002c0002t0016g0009 | 2 | NA19057.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.645-5623A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482918 | ||||||
chr4:110482994
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.645-5547G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110482994 | ||||||
chr4:110483173
|
C | G | 6 | a0001c0007t0003g0022a0003c0003t0002g0021a0003c0003t0002g0279others(3): Show | 7 | HG01975.hp2 HG02109.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-5368C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483173 | ||||||
chr4:110483222
|
T | C | 1 | a0002c0002t0003g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.645-5319T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483222 | ||||||
chr4:110483254
|
T | C | 196 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(193): Show | 209 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.645-5287T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483254 | ||||||
chr4:110483257
|
A | G | 196 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(193): Show | 209 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.645-5284A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483257 | ||||||
chr4:110483555
|
A | G | 37 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0053others(34): Show | 42 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.645-4986A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483555 | ||||||
chr4:110483619
|
A | G | 76 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0001g0111others(73): Show | 81 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.645-4922A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483619 | ||||||
chr4:110483630
|
A | G | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.645-4911A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483630 | ||||||
chr4:110483723
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.645-4818A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483723 | ||||||
chr4:110483774
|
C | T | 1 | a0002c0002t0002g0152 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.645-4767C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483774 | ||||||
chr4:110483819
|
C | T | 4 | a0001c0001t0002g0144a0001c0001t0005g0145a0001c0001t0027g0142others(1): Show | 4 | HG02622.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.645-4722C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110483819 | ||||||
chr4:110484037
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.645-4504C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110484037 | ||||||
chr4:110484128
|
G | A | 1 | a0006c0008t0004g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.645-4413G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110484128 | ||||||
chr4:110484476
|
G | C | 76 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0001g0116others(73): Show | 82 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.645-4065G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110484476 | ||||||
chr4:110484770
|
T | TTA | 123 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0052others(120): Show | 136 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.645-3757_645-3756d others(4): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 110484770 | |||||
chr4:110484770
|
T | TTATA | 3 | a0002c0002t0001g0080a0002c0002t0001g0081a0003c0003t0001g0275 | 3 | HG02080.hp1 HG02145.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.645-3759_645-3756d others(6): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 110484770 | |||||
chr4:110484853
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.645-3688G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110484853 | ||||||
chr4:110484920
|
T | TGCAC | 97 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 100 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.645-3612_645-3609d others(6): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 110484920 | |||||
chr4:110485340
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 113 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.645-3201G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110485340 | ||||||
chr4:110485437
|
A | C | 70 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0001g0116others(67): Show | 75 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.645-3104A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110485437 | ||||||
chr4:110485480
|
C | A | 1 | a0004c0004t0001g0233 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.645-3061C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110485480 | ||||||
chr4:110485482
|
C | CG | 8 | a0001c0001t0001g0013a0001c0001t0001g0217a0001c0001t0001g0218others(5): Show | 9 | HG00423.hp1 HG00621.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.645-3054dupG | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 110485482 | |||||
chr4:110485569
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.645-2972T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110485569 | ||||||
chr4:110485642
|
G | A | 1 | a0001c0001t0007g0284 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.645-2899G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110485642 | ||||||
chr4:110485885
|
T | C | 1 | a0003c0003t0010g0237 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.645-2656T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110485885 | ||||||
chr4:110485909
|
A | G | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.645-2632A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110485909 | ||||||
chr4:110485964
|
G | A | 1 | a0002c0002t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.645-2577G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110485964 | ||||||
chr4:110485984
|
A | G | 2 | a0002c0002t0001g0105a0002c0002t0001g0106 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.645-2557A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110485984 | ||||||
chr4:110486053
|
C | T | 3 | a0003c0003t0004g0273a0003c0003t0004g0274a0003c0003t0010g0237 | 3 | HG00741.hp1 HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.645-2488C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486053 | ||||||
chr4:110486173
|
T | G | 1 | a0002c0002t0005g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.645-2368T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486173 | ||||||
chr4:110486295
|
G | A | 191 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(188): Show | 203 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.645-2246G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486295 | ||||||
chr4:110486323
|
C | T | 191 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(188): Show | 203 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.645-2218C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486323 | ||||||
chr4:110486401
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.645-2140C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486401 | ||||||
chr4:110486577
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.645-1964G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486577 | ||||||
chr4:110486676
|
A | T | 192 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(189): Show | 204 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.645-1865A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486676 | ||||||
chr4:110486707
|
C | T | 1 | a0001c0001t0002g0221 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.645-1834C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486707 | ||||||
chr4:110486838
|
C | T | 1 | a0004c0004t0002g0271 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.645-1703C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486838 | ||||||
chr4:110486904
|
A | G | 2 | a0002c0002t0005g0049a0002c0002t0005g0050 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.645-1637A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110486904 | ||||||
chr4:110487527
|
C | T | 155 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(152): Show | 167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.645-1014C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110487527 | ||||||
chr4:110487562
|
G | A | 233 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(230): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.645-979G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110487562 | ||||||
chr4:110487760
|
AAT | A | 7 | a0003c0003t0001g0275a0003c0003t0002g0021a0003c0003t0002g0279others(4): Show | 8 | HG01975.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-778_645-777del others(2): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 110487760 | |||||
chr4:110487898
|
T | C | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.645-643T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110487898 | ||||||
chr4:110487958
|
T | A | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.645-583T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110487958 | ||||||
chr4:110488250
|
G | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.645-291G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110488250 | ||||||
chr4:110488277
|
A | G | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.645-264A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110488277 | ||||||
chr4:110488329
|
A | C | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG00609.hp2 NA18943.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.645-212A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110488329 | ||||||
chr4:110488465
|
T | C | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.645-76T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 1/19 | chr4 | 110488465 | ||||||
chr4:110488769
|
A | G | 66 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0116others(63): Show | 68 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.786+87A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110488769 | ||||||
chr4:110488850
|
T | C | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.786+168T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110488850 | ||||||
chr4:110488878
|
T | C | 1 | a0003c0003t0002g0021 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.786+196T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110488878 | ||||||
chr4:110488881
|
G | A | 1 | a0002c0002t0002g0082 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.786+199G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110488881 | ||||||
chr4:110489141
|
G | A | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.786+459G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110489141 | ||||||
chr4:110489210
|
GA | G | 6 | a0001c0001t0001g0102a0001c0001t0002g0210a0001c0001t0006g0103others(3): Show | 7 | HG01975.hp2 HG02027.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+540delA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr4 | 110489210 | |||||
chr4:110489326
|
G | A | 57 | a0002c0002t0001g0005a0002c0002t0001g0024a0002c0002t0001g0025others(54): Show | 62 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.786+644G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110489326 | ||||||
chr4:110489429
|
C | T | 1 | a0002c0002t0003g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.786+747C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110489429 | ||||||
chr4:110489496
|
G | A | 1 | a0002c0002t0004g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.786+814G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110489496 | ||||||
chr4:110489516
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.786+834C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110489516 | ||||||
chr4:110489674
|
T | G | 243 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(240): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.786+992T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110489674 | ||||||
chr4:110489710
|
G | T | 5 | a0001c0001t0001g0225a0001c0007t0001g0143a0001c0007t0003g0022others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+1028G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110489710 | ||||||
chr4:110489782
|
T | C | 1 | a0006c0008t0021g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.786+1100T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110489782 | ||||||
chr4:110489882
|
T | C | 3 | a0001c0007t0001g0143a0001c0007t0003g0022a0006c0021t0001g0167 | 3 | HG02109.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.787-1151T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110489882 | ||||||
chr4:110490038
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.787-995C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110490038 | ||||||
chr4:110490120
|
A | C | 1 | a0001c0001t0002g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.787-913A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110490120 | ||||||
chr4:110490180
|
GGAA | G | 4 | a0001c0001t0001g0225a0001c0007t0001g0143a0001c0007t0003g0022others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-848_787-846del others(3): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr4 | 110490180 | |||||
chr4:110490218
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230others(2): Show | 6 | HG01255.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-815A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110490218 | ||||||
chr4:110490246
|
G | C | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.787-787G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110490246 | ||||||
chr4:110490330
|
G | A | 1 | a0001c0001t0012g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.787-703G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110490330 | ||||||
chr4:110490381
|
G | T | 2 | a0001c0001t0005g0179a0001c0001t0005g0180 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.787-652G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110490381 | ||||||
chr4:110490551
|
C | G | 1 | a0001c0001t0018g0072 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.787-482C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110490551 | ||||||
chr4:110490866
|
A | T | 2 | a0001c0001t0001g0055a0001c0001t0020g0178 | 2 | NA18974.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.787-167A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110490866 | ||||||
chr4:110490932
|
C | A | 2 | a0013c0019t0011g0285a0017c0022t0001g0158 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.787-101C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 2/19 | chr4 | 110490932 | ||||||
chr4:110491230
|
G | A | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.918+66G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491230 | ||||||
chr4:110491235
|
GT | G | 170 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(167): Show | 185 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.918+88delT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 110491235 | |||||
chr4:110491340
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0003g0209 | 2 | HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.918+176A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491340 | ||||||
chr4:110491668
|
A | G | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.918+504A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491668 | ||||||
chr4:110491677
|
T | A | 174 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(171): Show | 188 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.918+513T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491677 | ||||||
chr4:110491714
|
CTTTCTTT others(5): Show |
C | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(95): Show | 102 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.918+554_918+565del others(12): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 110491714 | |||||
chr4:110491718
|
CT | C | 49 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0070others(46): Show | 55 | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.918+574delT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 110491718 | |||||
chr4:110491718
|
CTT | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0047a0001c0001t0001g0055others(21): Show | 26 | HG00280.hp2 HG00735.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.918+573_918+574del others(2): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 110491718 | |||||
chr4:110491722
|
T | C | 1 | a0017c0022t0001g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.918+558T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491722 | ||||||
chr4:110491741
|
G | T | 1 | a0002c0002t0002g0266 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.918+577G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491741 | ||||||
chr4:110491743
|
C | T | 148 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.918+579C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491743 | ||||||
chr4:110491809
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230 | 4 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+645C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491809 | ||||||
chr4:110491869
|
C | T | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.918+705C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491869 | ||||||
chr4:110491909
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.918+745C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491909 | ||||||
chr4:110491910
|
G | A | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.918+746G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110491910 | ||||||
chr4:110491940
|
C | CT | 29 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0111others(26): Show | 31 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.918+777dupT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 110491940 | |||||
chr4:110492023
|
A | G | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.918+859A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110492023 | ||||||
chr4:110492025
|
C | T | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.918+861C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110492025 | ||||||
chr4:110492286
|
G | T | 5 | a0003c0003t0002g0021a0003c0003t0002g0279a0003c0003t0004g0281others(2): Show | 6 | HG01975.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+1122G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110492286 | ||||||
chr4:110492518
|
C | T | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.918+1354C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110492518 | ||||||
chr4:110492712
|
A | C | 1 | a0002c0002t0001g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.918+1548A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110492712 | ||||||
chr4:110492803
|
C | T | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.918+1639C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110492803 | ||||||
chr4:110492809
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.918+1645G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110492809 | ||||||
chr4:110492852
|
C | T | 1 | a0010c0016t0006g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.918+1688C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110492852 | ||||||
chr4:110492911
|
A | G | 1 | a0017c0022t0001g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.918+1747A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110492911 | ||||||
chr4:110493243
|
T | C | 181 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(178): Show | 195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.918+2079T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110493243 | ||||||
chr4:110493244
|
A | G | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.918+2080A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110493244 | ||||||
chr4:110493300
|
A | T | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+2136A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110493300 | ||||||
chr4:110493311
|
G | A | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.918+2147G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110493311 | ||||||
chr4:110493335
|
A | G | 3 | a0002c0002t0001g0024a0005c0005t0001g0159a0015c0017t0002g0229 | 3 | HG02572.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.918+2171A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110493335 | ||||||
chr4:110493581
|
A | T | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(95): Show | 102 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.918+2417A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110493581 | ||||||
chr4:110494058
|
G | A | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.918+2894G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110494058 | ||||||
chr4:110494118
|
C | T | 4 | a0001c0001t0001g0177a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG02602.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+2954C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110494118 | ||||||
chr4:110494463
|
T | C | 1 | a0013c0019t0011g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.918+3299T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110494463 | ||||||
chr4:110494620
|
A | G | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.918+3456A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110494620 | ||||||
chr4:110494910
|
T | C | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.918+3746T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110494910 | ||||||
chr4:110495094
|
G | C | 1 | a0001c0001t0006g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.918+3930G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495094 | ||||||
chr4:110495126
|
A | C | 178 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(175): Show | 192 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.918+3962A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495126 | ||||||
chr4:110495129
|
A | G | 1 | a0006c0008t0004g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.918+3965A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495129 | ||||||
chr4:110495136
|
A | G | 106 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(103): Show | 111 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.918+3972A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495136 | ||||||
chr4:110495299
|
G | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+4135G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495299 | ||||||
chr4:110495421
|
G | A | 1 | a0002c0002t0001g0222 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.918+4257G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495421 | ||||||
chr4:110495468
|
C | A | 1 | a0003c0003t0003g0015 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.918+4304C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495468 | ||||||
chr4:110495470
|
C | A | 1 | a0003c0003t0003g0015 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.918+4306C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495470 | ||||||
chr4:110495669
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.918+4505C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495669 | ||||||
chr4:110495802
|
C | A | 15 | a0002c0002t0001g0079a0002c0002t0002g0101a0002c0002t0002g0147others(12): Show | 16 | HG00735.hp1 HG02083.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.918+4638C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495802 | ||||||
chr4:110495870
|
T | C | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.918+4706T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495870 | ||||||
chr4:110495998
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.918+4834T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110495998 | ||||||
chr4:110496271
|
A | T | 59 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(56): Show | 68 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.918+5107A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110496271 | ||||||
chr4:110496285
|
A | G | 1 | a0002c0002t0005g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.918+5121A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110496285 | ||||||
chr4:110496508
|
C | A | 76 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(73): Show | 86 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.918+5344C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110496508 | ||||||
chr4:110496634
|
C | T | 1 | a0002c0002t0005g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.918+5470C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110496634 | ||||||
chr4:110496665
|
T | A | 100 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(97): Show | 104 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.918+5501T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110496665 | ||||||
chr4:110496704
|
A | T | 75 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(72): Show | 85 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.918+5540A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110496704 | ||||||
chr4:110496929
|
T | G | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.918+5765T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110496929 | ||||||
chr4:110496940
|
C | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 67 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.918+5776C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110496940 | ||||||
chr4:110497091
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.918+5927C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497091 | ||||||
chr4:110497236
|
C | T | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+6072C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497236 | ||||||
chr4:110497300
|
G | GT | 5 | a0003c0003t0002g0021a0003c0003t0002g0279a0003c0003t0004g0281others(2): Show | 6 | HG01975.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+6144dupT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 110497300 | |||||
chr4:110497308
|
T | A | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(42): Show | 51 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.918+6144T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497308 | ||||||
chr4:110497372
|
A | T | 181 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(178): Show | 195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.918+6208A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497372 | ||||||
chr4:110497393
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.918+6229C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497393 | ||||||
chr4:110497397
|
G | A | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.918+6233G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497397 | ||||||
chr4:110497410
|
T | C | 1 | a0005c0005t0007g0011 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.918+6246T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497410 | ||||||
chr4:110497472
|
T | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 5 | HG00438.hp1 NA18952.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+6308T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497472 | ||||||
chr4:110497515
|
TA | T | 17 | a0002c0002t0001g0079a0002c0002t0002g0101a0002c0002t0002g0147others(14): Show | 18 | HG00735.hp1 HG01891.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.918+6356delA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 110497515 | |||||
chr4:110497532
|
T | C | 1 | a0002c0002t0005g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.918+6368T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497532 | ||||||
chr4:110497552
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.918+6388A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497552 | ||||||
chr4:110497618
|
G | A | 186 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(183): Show | 201 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.918+6454G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497618 | ||||||
chr4:110497620
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.918+6456G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497620 | ||||||
chr4:110497658
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(55): Show | 67 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.918+6494G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497658 | ||||||
chr4:110497771
|
A | G | 1 | a0003c0012t0003g0278 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.918+6607A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497771 | ||||||
chr4:110497805
|
A | G | 2 | a0003c0003t0004g0273a0003c0003t0004g0274 | 2 | HG00741.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.918+6641A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497805 | ||||||
chr4:110497900
|
T | C | 188 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(185): Show | 203 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.918+6736T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497900 | ||||||
chr4:110497951
|
A | G | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.918+6787A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110497951 | ||||||
chr4:110498041
|
G | A | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(95): Show | 102 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.918+6877G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498041 | ||||||
chr4:110498053
|
T | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(56): Show | 68 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.918+6889T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498053 | ||||||
chr4:110498102
|
G | A | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(42): Show | 51 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.918+6938G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498102 | ||||||
chr4:110498143
|
A | G | 76 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(73): Show | 86 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.918+6979A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498143 | ||||||
chr4:110498353
|
C | CA | 183 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(180): Show | 197 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.918+7197dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 110498353 | |||||
chr4:110498401
|
G | A | 3 | a0005c0005t0001g0153a0005c0005t0007g0154a0005c0005t0007g0155 | 3 | HG02486.hp2 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.918+7237G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498401 | ||||||
chr4:110498459
|
A | G | 5 | a0003c0003t0002g0021a0003c0003t0002g0279a0003c0003t0004g0281others(2): Show | 6 | HG01975.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+7295A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498459 | ||||||
chr4:110498617
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.918+7453A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498617 | ||||||
chr4:110498643
|
C | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+7479C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498643 | ||||||
chr4:110498691
|
T | C | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.918+7527T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498691 | ||||||
chr4:110498721
|
C | T | 3 | a0003c0003t0004g0281a0003c0003t0007g0280a0003c0012t0003g0278 | 3 | HG02965.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.918+7557C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498721 | ||||||
chr4:110498846
|
C | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0225a0001c0001t0001g0231others(10): Show | 16 | HG00544.hp2 HG02027.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.918+7682C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110498846 | ||||||
chr4:110499127
|
T | A | 152 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(149): Show | 163 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.919-7510T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499127 | ||||||
chr4:110499154
|
C | T | 2 | a0003c0003t0004g0281a0003c0003t0007g0280 | 2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.919-7483C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499154 | ||||||
chr4:110499413
|
C | G | 1 | a0002c0002t0004g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.919-7224C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499413 | ||||||
chr4:110499421
|
G | A | 242 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(239): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.919-7216G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499421 | ||||||
chr4:110499488
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00741.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.919-7149A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499488 | ||||||
chr4:110499617
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.919-7020C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499617 | ||||||
chr4:110499723
|
A | T | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.919-6914A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499723 | ||||||
chr4:110499899
|
G | A | 2 | a0003c0003t0001g0275a0003c0003t0002g0282 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.919-6738G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499899 | ||||||
chr4:110499936
|
T | C | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.919-6701T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499936 | ||||||
chr4:110499939
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.919-6698C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499939 | ||||||
chr4:110499998
|
C | T | 3 | a0003c0003t0004g0281a0003c0003t0007g0280a0003c0012t0003g0278 | 3 | HG02965.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.919-6639C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110499998 | ||||||
chr4:110500028
|
G | A | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.919-6609G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110500028 | ||||||
chr4:110500063
|
A | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0207 | 2 | HG00408.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.919-6574A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110500063 | ||||||
chr4:110500149
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.919-6488G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110500149 | ||||||
chr4:110500287
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.919-6350A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110500287 | ||||||
chr4:110500604
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.919-6033G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110500604 | ||||||
chr4:110500620
|
C | A | 219 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(216): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.919-6017C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110500620 | ||||||
chr4:110500714
|
T | C | 3 | a0003c0003t0004g0281a0003c0003t0007g0280a0003c0012t0003g0278 | 3 | HG02965.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.919-5923T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110500714 | ||||||
chr4:110500794
|
G | A | 1 | a0001c0001t0028g0184 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.919-5843G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110500794 | ||||||
chr4:110500939
|
C | T | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.919-5698C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110500939 | ||||||
chr4:110501059
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.919-5578G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501059 | ||||||
chr4:110501067
|
C | T | 284 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(281): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.919-5570C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501067 | ||||||
chr4:110501308
|
A | G | 6 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0002g0203others(3): Show | 6 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.919-5329A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501308 | ||||||
chr4:110501317
|
T | C | 1 | a0003c0003t0010g0237 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.919-5320T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501317 | ||||||
chr4:110501403
|
C | T | 1 | a0001c0007t0003g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.919-5234C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501403 | ||||||
chr4:110501659
|
C | A | 17 | a0002c0002t0001g0079a0002c0002t0002g0101a0002c0002t0002g0147others(14): Show | 19 | HG00735.hp1 HG01975.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.919-4978C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501659 | ||||||
chr4:110501711
|
C | T | 78 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(75): Show | 89 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.919-4926C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501711 | ||||||
chr4:110501743
|
A | G | 3 | a0002c0002t0001g0024a0005c0005t0001g0159a0015c0017t0002g0229 | 3 | HG02572.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.919-4894A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501743 | ||||||
chr4:110501817
|
C | A | 1 | a0002c0002t0001g0241 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.919-4820C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501817 | ||||||
chr4:110501983
|
T | C | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.919-4654T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110501983 | ||||||
chr4:110502036
|
T | A | 3 | a0002c0002t0003g0030a0002c0006t0001g0029a0002c0006t0012g0028 | 3 | HG00280.hp1 HG01256.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.919-4601T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110502036 | ||||||
chr4:110502158
|
G | A | 60 | a0002c0002t0001g0005a0002c0002t0001g0025a0002c0002t0001g0032others(57): Show | 65 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.919-4479G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110502158 | ||||||
chr4:110502166
|
C | T | 3 | a0003c0003t0004g0281a0003c0003t0007g0280a0003c0012t0003g0278 | 3 | HG02965.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.919-4471C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110502166 | ||||||
chr4:110502228
|
A | G | 1 | a0002c0002t0001g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.919-4409A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110502228 | ||||||
chr4:110502340
|
G | T | 1 | a0009c0013t0001g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.919-4297G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110502340 | ||||||
chr4:110502378
|
C | G | 3 | a0002c0002t0001g0024a0005c0005t0001g0159a0015c0017t0002g0229 | 3 | HG02572.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.919-4259C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110502378 | ||||||
chr4:110502465
|
G | A | 3 | a0001c0001t0002g0104a0001c0001t0002g0183a0001c0001t0002g0186 | 3 | HG01975.hp1 NA18961.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.919-4172G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110502465 | ||||||
chr4:110502895
|
C | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.919-3742C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110502895 | ||||||
chr4:110502940
|
G | A | 173 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(170): Show | 187 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.919-3697G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110502940 | ||||||
chr4:110503016
|
T | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.919-3621T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503016 | ||||||
chr4:110503024
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230others(1): Show | 5 | HG01255.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.919-3613A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503024 | ||||||
chr4:110503042
|
T | C | 60 | a0002c0002t0001g0005a0002c0002t0001g0025a0002c0002t0001g0032others(57): Show | 65 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.919-3595T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503042 | ||||||
chr4:110503061
|
C | A | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919-3576C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503061 | ||||||
chr4:110503132
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.919-3505C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503132 | ||||||
chr4:110503151
|
A | G | 177 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(174): Show | 192 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.919-3486A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503151 | ||||||
chr4:110503235
|
G | C | 181 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(178): Show | 196 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.919-3402G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503235 | ||||||
chr4:110503275
|
G | A | 149 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(146): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.919-3362G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503275 | ||||||
chr4:110503442
|
A | G | 60 | a0002c0002t0001g0005a0002c0002t0001g0025a0002c0002t0001g0032others(57): Show | 65 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.919-3195A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503442 | ||||||
chr4:110503560
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.919-3077C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503560 | ||||||
chr4:110503611
|
C | A | 173 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(170): Show | 187 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.919-3026C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503611 | ||||||
chr4:110503689
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230others(1): Show | 5 | HG01255.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.919-2948A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503689 | ||||||
chr4:110503799
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.919-2838G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503799 | ||||||
chr4:110503911
|
A | C | 2 | a0001c0001t0005g0067a0001c0001t0011g0068 | 2 | HG01243.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.919-2726A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110503911 | ||||||
chr4:110504040
|
T | A | 24 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(21): Show | 28 | HG00544.hp2 HG00735.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.919-2597T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504040 | ||||||
chr4:110504211
|
C | T | 2 | a0013c0019t0011g0285a0017c0022t0001g0158 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.919-2426C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504211 | ||||||
chr4:110504230
|
T | C | 1 | a0002c0002t0001g0239 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.919-2407T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504230 | ||||||
chr4:110504255
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.919-2382T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504255 | ||||||
chr4:110504499
|
G | C | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.919-2138G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504499 | ||||||
chr4:110504585
|
C | G | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.919-2052C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504585 | ||||||
chr4:110504678
|
G | C | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919-1959G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504678 | ||||||
chr4:110504739
|
A | G | 104 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(101): Show | 108 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.919-1898A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504739 | ||||||
chr4:110504865
|
C | T | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.919-1772C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504865 | ||||||
chr4:110504871
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.919-1766C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504871 | ||||||
chr4:110504939
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230 | 4 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-1698G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504939 | ||||||
chr4:110504978
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0007g0284 | 2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.919-1659G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504978 | ||||||
chr4:110504983
|
A | G | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.919-1654A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110504983 | ||||||
chr4:110505025
|
T | C | 3 | a0002c0002t0001g0024a0005c0005t0001g0159a0015c0017t0002g0229 | 3 | HG02572.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.919-1612T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110505025 | ||||||
chr4:110505142
|
G | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.919-1495G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110505142 | ||||||
chr4:110505185
|
T | C | 57 | a0002c0002t0001g0005a0002c0002t0001g0025a0002c0002t0001g0032others(54): Show | 62 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.919-1452T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110505185 | ||||||
chr4:110505301
|
C | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(43): Show | 52 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.919-1336C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110505301 | ||||||
chr4:110505761
|
T | A | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919-876T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110505761 | ||||||
chr4:110506214
|
CAGAGAA | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(72): Show | 85 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.919-406_919-401del others(6): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 110506214 | |||||
chr4:110506308
|
A | G | 2 | a0001c0001t0005g0179a0001c0001t0005g0180 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.919-329A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110506308 | ||||||
chr4:110506383
|
C | T | 3 | a0003c0003t0001g0018a0003c0003t0001g0264a0003c0003t0002g0263 | 4 | NA18941.hp2 NA18995.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-254C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110506383 | ||||||
chr4:110506465
|
G | T | 1 | a0013c0019t0011g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.919-172G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 3/19 | chr4 | 110506465 | ||||||
chr4:110506775
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1039+18A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110506775 | ||||||
chr4:110507084
|
T | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039+327T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110507084 | ||||||
chr4:110507197
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1039+440C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110507197 | ||||||
chr4:110507523
|
T | C | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1039+766T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110507523 | ||||||
chr4:110507596
|
G | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039+839G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110507596 | ||||||
chr4:110507676
|
A | G | 3 | a0002c0002t0001g0024a0005c0005t0001g0159a0015c0017t0002g0229 | 3 | HG02572.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1039+919A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110507676 | ||||||
chr4:110507764
|
C | T | 1 | a0010c0016t0006g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1039+1007C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110507764 | ||||||
chr4:110507832
|
A | C | 1 | a0001c0001t0002g0073 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1039+1075A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110507832 | ||||||
chr4:110507926
|
G | A | 2 | a0001c0001t0015g0059a0001c0001t0019g0060 | 2 | NA18968.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1039+1169G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110507926 | ||||||
chr4:110508269
|
C | CA | 120 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(117): Show | 129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1040-1365dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 110508269 | |||||
chr4:110508269
|
C | CAA | 6 | a0001c0001t0001g0102a0001c0001t0001g0111a0001c0001t0001g0163others(3): Show | 6 | HG01346.hp1 HG03669.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040-1366_1040-136 others(6): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 110508269 | |||||
chr4:110508269
|
CA | C | 8 | a0002c0002t0001g0024a0002c0002t0001g0079a0002c0002t0001g0096others(5): Show | 8 | HG00140.hp1 HG01106.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040-1365delA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 110508269 | |||||
chr4:110508269
|
CAA | C | 30 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0002g0004others(27): Show | 35 | HG00544.hp2 HG00735.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.1040-1366_1040-136 others(6): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 110508269 | |||||
chr4:110508289
|
T | A | 6 | a0002c0002t0001g0005a0002c0002t0001g0032a0002c0002t0001g0033others(3): Show | 9 | HG01517.hp1 HG02004.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1040-1364T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110508289 | ||||||
chr4:110508290
|
G | C | 1 | a0002c0002t0001g0086 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1040-1363G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110508290 | ||||||
chr4:110508430
|
T | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 5 | HG00438.hp1 NA18952.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1040-1223T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110508430 | ||||||
chr4:110508479
|
A | C | 1 | a0005c0005t0007g0011 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1040-1174A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110508479 | ||||||
chr4:110508537
|
T | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(72): Show | 85 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1040-1116T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110508537 | ||||||
chr4:110508600
|
A | G | 3 | a0002c0002t0005g0026a0002c0002t0005g0043a0002c0002t0005g0044 | 3 | HG02280.hp2 HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1040-1053A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110508600 | ||||||
chr4:110508605
|
A | G | 1 | a0001c0001t0005g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1040-1048A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110508605 | ||||||
chr4:110508728
|
G | A | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1040-925G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110508728 | ||||||
chr4:110508904
|
C | T | 51 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(48): Show | 57 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1040-749C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110508904 | ||||||
chr4:110509132
|
G | A | 1 | a0013c0019t0011g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1040-521G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110509132 | ||||||
chr4:110509162
|
G | A | 1 | a0002c0002t0004g0034 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1040-491G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110509162 | ||||||
chr4:110509193
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1040-460C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110509193 | ||||||
chr4:110509354
|
G | A | 7 | a0001c0001t0002g0120a0001c0001t0002g0122a0001c0001t0004g0121others(4): Show | 7 | HG00621.hp1 HG02602.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1040-299G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110509354 | ||||||
chr4:110509396
|
T | A | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1040-257T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110509396 | ||||||
chr4:110509482
|
C | T | 241 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(238): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1040-171C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110509482 | ||||||
chr4:110509512
|
A | G | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1040-141A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110509512 | ||||||
chr4:110509613
|
A | G | 2 | a0013c0019t0011g0285a0017c0022t0001g0158 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1040-40A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 4/19 | chr4 | 110509613 | ||||||
chr4:110510007
|
G | A | 1 | a0002c0002t0003g0003 | 3 | HG01517.hp1 HG03669.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1194+200G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 5/19 | chr4 | 110510007 | ||||||
chr4:110510026
|
A | G | 57 | a0002c0002t0001g0005a0002c0002t0001g0025a0002c0002t0001g0032others(54): Show | 62 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1194+219A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 5/19 | chr4 | 110510026 | ||||||
chr4:110510129
|
G | A | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1195-116G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 5/19 | chr4 | 110510129 | ||||||
chr4:110510441
|
C | T | 2 | a0013c0019t0011g0285a0017c0022t0001g0158 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1308+83C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110510441 | ||||||
chr4:110510443
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1308+85A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110510443 | ||||||
chr4:110510607
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1308+249C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110510607 | ||||||
chr4:110510610
|
G | GA | 7 | a0002c0002t0001g0025a0002c0002t0001g0243a0002c0002t0004g0035others(4): Show | 7 | HG00673.hp2 HG01070.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1308+268dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr4 | 110510610 | |||||
chr4:110510610
|
GA | G | 130 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0102others(127): Show | 136 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1308+268delA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr4 | 110510610 | |||||
chr4:110510610
|
GAA | G | 5 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0078others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1308+267_1308+268d others(4): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr4 | 110510610 | |||||
chr4:110510660
|
A | G | 47 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(44): Show | 53 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.1308+302A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110510660 | ||||||
chr4:110510885
|
C | T | 174 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(171): Show | 188 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1308+527C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110510885 | ||||||
chr4:110510923
|
T | C | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1308+565T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110510923 | ||||||
chr4:110510925
|
A | G | 1 | a0001c0001t0005g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1308+567A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110510925 | ||||||
chr4:110511049
|
A | G | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1308+691A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511049 | ||||||
chr4:110511247
|
A | G | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1308+889A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511247 | ||||||
chr4:110511306
|
G | C | 12 | a0002c0002t0002g0101a0002c0002t0002g0147a0002c0002t0003g0058others(9): Show | 13 | HG00735.hp1 HG01975.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1308+948G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511306 | ||||||
chr4:110511444
|
C | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(47): Show | 56 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1308+1086C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511444 | ||||||
chr4:110511514
|
A | G | 1 | a0002c0002t0004g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1308+1156A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511514 | ||||||
chr4:110511552
|
C | G | 69 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230others(66): Show | 75 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1308+1194C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511552 | ||||||
chr4:110511609
|
T | C | 3 | a0003c0003t0004g0281a0003c0003t0007g0280a0003c0012t0003g0278 | 3 | HG02965.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1308+1251T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511609 | ||||||
chr4:110511685
|
G | A | 69 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230others(66): Show | 75 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1308+1327G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511685 | ||||||
chr4:110511698
|
G | A | 69 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230others(66): Show | 75 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1308+1340G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511698 | ||||||
chr4:110511761
|
CT | C | 69 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0002g0004others(66): Show | 77 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1308+1416delT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr4 | 110511761 | |||||
chr4:110511851
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1308+1493C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511851 | ||||||
chr4:110511920
|
C | T | 57 | a0002c0002t0001g0005a0002c0002t0001g0025a0002c0002t0001g0032others(54): Show | 62 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1309-1495C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110511920 | ||||||
chr4:110512013
|
C | G | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1309-1402C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512013 | ||||||
chr4:110512054
|
G | A | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-1361G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512054 | ||||||
chr4:110512061
|
G | A | 59 | a0002c0002t0001g0005a0002c0002t0001g0025a0002c0002t0001g0032others(56): Show | 64 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1309-1354G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512061 | ||||||
chr4:110512188
|
A | G | 1 | a0001c0001t0006g0119 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1309-1227A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512188 | ||||||
chr4:110512253
|
C | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(43): Show | 52 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1309-1162C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512253 | ||||||
chr4:110512291
|
A | G | 1 | a0002c0002t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1309-1124A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512291 | ||||||
chr4:110512336
|
G | A | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1309-1079G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512336 | ||||||
chr4:110512466
|
T | C | 1 | a0001c0001t0002g0150 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1309-949T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512466 | ||||||
chr4:110512493
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0006g0103a0001c0001t0022g0124 | 3 | HG02698.hp2 HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1309-922C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512493 | ||||||
chr4:110512496
|
T | C | 1 | a0001c0001t0004g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1309-919T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512496 | ||||||
chr4:110512576
|
A | G | 3 | a0002c0002t0004g0041a0002c0002t0005g0049a0002c0002t0005g0050 | 3 | HG02145.hp1 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1309-839A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512576 | ||||||
chr4:110512775
|
T | C | 2 | a0003c0003t0004g0273a0003c0003t0004g0274 | 2 | HG00741.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1309-640T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512775 | ||||||
chr4:110512896
|
C | G | 3 | a0003c0003t0004g0281a0003c0003t0007g0280a0003c0012t0003g0278 | 3 | HG02965.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1309-519C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512896 | ||||||
chr4:110512927
|
G | A | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-488G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110512927 | ||||||
chr4:110513128
|
C | T | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-287C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110513128 | ||||||
chr4:110513250
|
T | C | 3 | a0003c0003t0004g0273a0003c0003t0004g0274a0003c0003t0010g0237 | 3 | HG00741.hp1 HG01175.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1309-165T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110513250 | ||||||
chr4:110513257
|
C | A | 1 | a0001c0001t0002g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1309-158C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 6/19 | chr4 | 110513257 | ||||||
chr4:110513712
|
G | A | 2 | a0002c0002t0005g0049a0002c0002t0005g0050 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1443+163G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110513712 | ||||||
chr4:110513765
|
T | C | 2 | a0001c0001t0005g0145a0014c0018t0013g0042 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1443+216T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110513765 | ||||||
chr4:110513964
|
T | A | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1443+415T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110513964 | ||||||
chr4:110514253
|
T | A | 174 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(171): Show | 188 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1443+704T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110514253 | ||||||
chr4:110514278
|
T | C | 174 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(171): Show | 188 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1443+729T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110514278 | ||||||
chr4:110514281
|
T | TA | 3 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230 | 4 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1443+733dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 110514281 | |||||
chr4:110514347
|
T | G | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1443+798T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110514347 | ||||||
chr4:110514460
|
T | G | 3 | a0001c0007t0001g0143a0001c0007t0003g0022a0006c0021t0001g0167 | 3 | HG02109.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1443+911T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110514460 | ||||||
chr4:110514496
|
G | A | 1 | a0003c0003t0001g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1444-881G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110514496 | ||||||
chr4:110514547
|
A | G | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1444-830A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110514547 | ||||||
chr4:110514700
|
T | TG | 174 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(171): Show | 188 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1444-672dupG | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 110514700 | |||||
chr4:110514773
|
C | T | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1444-604C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110514773 | ||||||
chr4:110514922
|
A | T | 4 | a0002c0002t0002g0168a0003c0003t0004g0281a0003c0003t0007g0280others(1): Show | 4 | HG01255.hp1 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444-455A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110514922 | ||||||
chr4:110515018
|
C | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1444-359C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110515018 | ||||||
chr4:110515100
|
G | C | 2 | a0002c0002t0001g0105a0002c0002t0001g0106 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1444-277G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110515100 | ||||||
chr4:110515322
|
A | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG01496.hp2 HG01981.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444-55A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110515322 | ||||||
chr4:110515352
|
A | G | 14 | a0002c0002t0002g0101a0002c0002t0002g0147a0002c0002t0003g0058others(11): Show | 15 | HG00735.hp1 HG01891.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1444-25A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 7/19 | chr4 | 110515352 | ||||||
chr4:110515585
|
C | G | 168 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(165): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1509+143C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110515585 | ||||||
chr4:110515912
|
G | A | 3 | a0002c0002t0002g0084a0002c0002t0004g0169a0002c0002t0016g0009 | 4 | HG02165.hp2 NA18747.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+470G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110515912 | ||||||
chr4:110515947
|
C | T | 243 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(240): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1509+505C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110515947 | ||||||
chr4:110515971
|
A | C | 185 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(182): Show | 200 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1509+529A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110515971 | ||||||
chr4:110516227
|
A | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230 | 4 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+785A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516227 | ||||||
chr4:110516271
|
G | A | 1 | a0002c0002t0001g0085 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1509+829G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516271 | ||||||
chr4:110516467
|
T | A | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1509+1025T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516467 | ||||||
chr4:110516486
|
C | G | 3 | a0003c0003t0004g0281a0003c0003t0007g0280a0003c0012t0003g0278 | 3 | HG02965.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1509+1044C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516486 | ||||||
chr4:110516494
|
T | C | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1509+1052T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516494 | ||||||
chr4:110516527
|
G | C | 1 | a0002c0002t0001g0025 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1509+1085G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516527 | ||||||
chr4:110516706
|
A | C | 3 | a0003c0003t0004g0281a0003c0003t0007g0280a0003c0012t0003g0278 | 3 | HG02965.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1509+1264A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516706 | ||||||
chr4:110516801
|
A | G | 1 | a0003c0012t0003g0278 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1509+1359A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516801 | ||||||
chr4:110516830
|
G | A | 15 | a0001c0001t0001g0008a0002c0002t0002g0101a0002c0002t0002g0147others(12): Show | 17 | HG00735.hp1 HG01891.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.1509+1388G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516830 | ||||||
chr4:110516969
|
A | C | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1509+1527A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516969 | ||||||
chr4:110516974
|
C | T | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1509+1532C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516974 | ||||||
chr4:110516975
|
G | A | 3 | a0001c0001t0002g0203a0002c0002t0001g0024a0005c0005t0001g0159 | 3 | HG02056.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1509+1533G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516975 | ||||||
chr4:110516990
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230 | 4 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+1548C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110516990 | ||||||
chr4:110517039
|
G | A | 2 | a0001c0001t0005g0145a0014c0018t0013g0042 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1509+1597G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517039 | ||||||
chr4:110517069
|
G | A | 2 | a0002c0002t0005g0049a0002c0002t0005g0050 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1509+1627G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517069 | ||||||
chr4:110517129
|
G | A | 1 | a0002c0002t0004g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1509+1687G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517129 | ||||||
chr4:110517167
|
T | C | 5 | a0001c0001t0002g0004a0001c0001t0002g0078a0001c0001t0002g0149others(2): Show | 7 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+1725T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517167 | ||||||
chr4:110517189
|
C | G | 3 | a0003c0003t0004g0281a0003c0003t0007g0280a0003c0012t0003g0278 | 3 | HG02965.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1509+1747C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517189 | ||||||
chr4:110517203
|
G | A | 173 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(170): Show | 187 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1509+1761G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517203 | ||||||
chr4:110517462
|
G | T | 13 | a0001c0001t0001g0008a0002c0002t0002g0101a0002c0002t0002g0147others(10): Show | 15 | HG00735.hp1 HG01975.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1509+2020G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517462 | ||||||
chr4:110517569
|
C | T | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+2127C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517569 | ||||||
chr4:110517764
|
G | A | 13 | a0001c0001t0001g0008a0002c0002t0002g0101a0002c0002t0002g0147others(10): Show | 15 | HG00735.hp1 HG01975.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1510-2244G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517764 | ||||||
chr4:110517851
|
T | A | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1510-2157T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517851 | ||||||
chr4:110517862
|
C | G | 58 | a0001c0001t0001g0102a0002c0002t0001g0005a0002c0002t0001g0025others(55): Show | 63 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1510-2146C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110517862 | ||||||
chr4:110518121
|
C | T | 1 | a0002c0002t0004g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1510-1887C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518121 | ||||||
chr4:110518310
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1510-1698T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518310 | ||||||
chr4:110518330
|
G | T | 59 | a0001c0001t0001g0102a0002c0002t0001g0005a0002c0002t0001g0025others(56): Show | 64 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1510-1678G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518330 | ||||||
chr4:110518386
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 5 | NA18942.hp2 NA18950.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510-1622T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518386 | ||||||
chr4:110518402
|
G | A | 1 | a0002c0002t0001g0086 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1510-1606G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518402 | ||||||
chr4:110518446
|
C | T | 44 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0055others(41): Show | 49 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1510-1562C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518446 | ||||||
chr4:110518551
|
C | G | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1510-1457C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518551 | ||||||
chr4:110518654
|
C | A | 1 | a0003c0012t0003g0278 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1510-1354C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518654 | ||||||
chr4:110518918
|
C | T | 78 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(75): Show | 89 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1510-1090C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518918 | ||||||
chr4:110518920
|
A | G | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1510-1088A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110518920 | ||||||
chr4:110519146
|
T | C | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0003g0069others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510-862T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519146 | ||||||
chr4:110519188
|
T | A | 2 | a0002c0002t0008g0037a0002c0002t0010g0036 | 2 | HG01074.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1510-820T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519188 | ||||||
chr4:110519229
|
C | T | 4 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0154others(1): Show | 4 | HG02486.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510-779C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519229 | ||||||
chr4:110519308
|
A | G | 1 | a0001c0001t0002g0199 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1510-700A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519308 | ||||||
chr4:110519606
|
T | C | 1 | a0002c0006t0012g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1510-402T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519606 | ||||||
chr4:110519617
|
T | TCCA | 43 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0055others(40): Show | 48 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1510-369_1510-367d others(5): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 110519617 | |||||
chr4:110519617
|
TCCA | T | 25 | a0002c0002t0001g0080a0002c0002t0001g0081a0002c0002t0001g0085others(22): Show | 26 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1510-369_1510-367d others(5): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 110519617 | |||||
chr4:110519639
|
CCAT | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0225others(29): Show | 38 | HG00544.hp2 HG00735.hp1 HG01975.hp2 others(35): Show |
intron_variant | MODIFIER | c.1510-359_1510-357d others(5): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 110519639 | |||||
chr4:110519642
|
T | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0055others(40): Show | 48 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1510-366T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519642 | ||||||
chr4:110519652
|
T | C | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(95): Show | 102 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1510-356T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519652 | ||||||
chr4:110519896
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1510-112C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519896 | ||||||
chr4:110519906
|
G | A | 1 | a0017c0022t0001g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1510-102G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519906 | ||||||
chr4:110519909
|
A | T | 1 | a0001c0001t0002g0199 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1510-99A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519909 | ||||||
chr4:110519989
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1510-19G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 8/19 | chr4 | 110519989 | ||||||
chr4:110520440
|
G | C | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1727+74G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520440 | ||||||
chr4:110520447
|
A | G | 1 | a0002c0002t0001g0223 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1727+81A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520447 | ||||||
chr4:110520475
|
A | G | 1 | a0002c0002t0002g0094 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1727+109A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520475 | ||||||
chr4:110520555
|
A | T | 2 | a0002c0002t0004g0027a0003c0003t0002g0282 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1727+189A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520555 | ||||||
chr4:110520570
|
G | A | 1 | a0003c0003t0001g0242 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1727+204G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520570 | ||||||
chr4:110520628
|
A | T | 1 | a0002c0002t0002g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1727+262A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520628 | ||||||
chr4:110520666
|
G | T | 4 | a0003c0003t0001g0275a0003c0003t0004g0281a0003c0003t0007g0280others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1727+300G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520666 | ||||||
chr4:110520711
|
T | C | 2 | a0002c0002t0004g0027a0003c0003t0002g0282 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1727+345T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520711 | ||||||
chr4:110520764
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1727+398C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520764 | ||||||
chr4:110520900
|
C | A | 1 | a0001c0001t0015g0059 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1727+534C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520900 | ||||||
chr4:110520938
|
A | G | 1 | a0002c0002t0002g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1727+572A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110520938 | ||||||
chr4:110521070
|
G | C | 1 | a0002c0002t0001g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1727+704G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110521070 | ||||||
chr4:110521093
|
C | A | 2 | a0002c0002t0004g0027a0003c0003t0002g0282 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1727+727C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110521093 | ||||||
chr4:110521210
|
T | A | 86 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 97 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1727+844T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110521210 | ||||||
chr4:110521523
|
C | A | 2 | a0002c0002t0004g0027a0003c0003t0002g0282 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1727+1157C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110521523 | ||||||
chr4:110521594
|
A | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00741.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1727+1228A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110521594 | ||||||
chr4:110521811
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1727+1445G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110521811 | ||||||
chr4:110521835
|
A | C | 1 | a0001c0001t0001g0198 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1727+1469A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110521835 | ||||||
chr4:110521852
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0002g0140 | 3 | HG02615.hp2 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1727+1486C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110521852 | ||||||
chr4:110521957
|
C | A | 2 | a0001c0001t0005g0179a0001c0001t0005g0180 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1727+1591C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110521957 | ||||||
chr4:110522016
|
T | C | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1727+1650T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522016 | ||||||
chr4:110522040
|
G | T | 1 | a0002c0002t0001g0170 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1727+1674G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522040 | ||||||
chr4:110522078
|
C | T | 4 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0154others(1): Show | 4 | HG02486.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1727+1712C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522078 | ||||||
chr4:110522189
|
C | CT | 6 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0231others(3): Show | 7 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1727+1834dupT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 110522189 | |||||
chr4:110522222
|
G | A | 2 | a0001c0001t0001g0208a0002c0002t0025g0244 | 2 | HG01261.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1727+1856G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522222 | ||||||
chr4:110522293
|
T | G | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1727+1927T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522293 | ||||||
chr4:110522431
|
T | C | 4 | a0001c0001t0002g0004a0001c0001t0002g0149a0001c0001t0002g0150others(1): Show | 6 | HG00544.hp2 HG02056.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1727+2065T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522431 | ||||||
chr4:110522470
|
C | T | 3 | a0001c0001t0015g0059a0001c0001t0019g0060a0015c0017t0002g0229 | 3 | HG02572.hp1 NA18968.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1727+2104C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522470 | ||||||
chr4:110522495
|
A | C | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1727+2129A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522495 | ||||||
chr4:110522609
|
C | T | 5 | a0001c0001t0001g0225a0001c0007t0001g0143a0001c0007t0003g0022others(2): Show | 6 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1727+2243C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522609 | ||||||
chr4:110522622
|
G | A | 284 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(281): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1727+2256G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522622 | ||||||
chr4:110522627
|
T | C | 1 | a0002c0002t0002g0147 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1727+2261T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522627 | ||||||
chr4:110522659
|
A | T | 1 | a0001c0001t0002g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1727+2293A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522659 | ||||||
chr4:110522711
|
G | A | 4 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0154others(1): Show | 4 | HG02486.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1727+2345G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110522711 | ||||||
chr4:110523216
|
A | G | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1727+2850A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110523216 | ||||||
chr4:110523379
|
C | T | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1727+3013C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110523379 | ||||||
chr4:110523520
|
G | A | 1 | a0003c0003t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1727+3154G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110523520 | ||||||
chr4:110523790
|
A | T | 29 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0111others(26): Show | 31 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1727+3424A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110523790 | ||||||
chr4:110523804
|
A | G | 1 | a0001c0001t0002g0139 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1727+3438A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110523804 | ||||||
chr4:110523806
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1727+3440G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110523806 | ||||||
chr4:110523852
|
G | A | 2 | a0013c0019t0011g0285a0017c0022t0001g0158 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1727+3486G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110523852 | ||||||
chr4:110524015
|
C | A | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1727+3649C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524015 | ||||||
chr4:110524332
|
G | A | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1727+3966G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524332 | ||||||
chr4:110524431
|
A | G | 146 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(143): Show | 158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1727+4065A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524431 | ||||||
chr4:110524435
|
A | G | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1727+4069A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524435 | ||||||
chr4:110524487
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1727+4121G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524487 | ||||||
chr4:110524500
|
A | G | 1 | a0001c0001t0004g0128 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1727+4134A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524500 | ||||||
chr4:110524540
|
G | A | 74 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(71): Show | 85 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1727+4174G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524540 | ||||||
chr4:110524600
|
T | A | 1 | a0003c0003t0002g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1727+4234T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524600 | ||||||
chr4:110524629
|
T | C | 1 | a0002c0002t0004g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1727+4263T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524629 | ||||||
chr4:110524715
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1727+4349C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524715 | ||||||
chr4:110524790
|
G | C | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1727+4424G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524790 | ||||||
chr4:110524926
|
T | C | 1 | a0002c0002t0002g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1727+4560T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110524926 | ||||||
chr4:110525204
|
T | C | 284 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(281): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1727+4838T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110525204 | ||||||
chr4:110525359
|
G | A | 1 | a0007c0010t0001g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1727+4993G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110525359 | ||||||
chr4:110525371
|
C | A | 4 | a0001c0001t0001g0188a0001c0001t0002g0199a0001c0001t0002g0206others(1): Show | 4 | HG02027.hp1 HG02083.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1727+5005C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110525371 | ||||||
chr4:110525476
|
C | CT | 115 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(112): Show | 133 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1727+5112dupT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 110525476 | |||||
chr4:110525483
|
C | T | 117 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(114): Show | 135 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1727+5117C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110525483 | ||||||
chr4:110525662
|
TTAACTC | T | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(95): Show | 102 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1727+5300_1727+530 others(10): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 110525662 | |||||
chr4:110525967
|
T | G | 284 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(281): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1728-5231T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110525967 | ||||||
chr4:110526001
|
C | T | 41 | a0002c0002t0001g0017a0002c0002t0001g0170a0002c0002t0001g0239others(38): Show | 48 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1728-5197C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526001 | ||||||
chr4:110526103
|
C | G | 58 | a0001c0001t0001g0102a0002c0002t0001g0005a0002c0002t0001g0025others(55): Show | 63 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1728-5095C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526103 | ||||||
chr4:110526153
|
G | C | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1728-5045G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526153 | ||||||
chr4:110526177
|
G | A | 74 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(71): Show | 85 | HG00280.hp2 HG00544.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1728-5021G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526177 | ||||||
chr4:110526240
|
C | T | 7 | a0001c0001t0001g0225a0001c0007t0001g0143a0001c0007t0003g0022others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1728-4958C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526240 | ||||||
chr4:110526291
|
A | C | 1 | a0005c0005t0007g0155 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1728-4907A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526291 | ||||||
chr4:110526302
|
C | G | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1728-4896C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526302 | ||||||
chr4:110526619
|
A | C | 1 | a0002c0002t0001g0170 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1728-4579A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526619 | ||||||
chr4:110526698
|
T | C | 47 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0047others(44): Show | 53 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.1728-4500T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526698 | ||||||
chr4:110526720
|
A | G | 4 | a0003c0003t0001g0275a0003c0003t0004g0281a0003c0003t0007g0280others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1728-4478A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526720 | ||||||
chr4:110526873
|
T | C | 1 | a0002c0002t0002g0147 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1728-4325T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526873 | ||||||
chr4:110526918
|
A | C | 1 | a0001c0001t0009g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1728-4280A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526918 | ||||||
chr4:110526985
|
G | A | 1 | a0002c0002t0005g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1728-4213G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110526985 | ||||||
chr4:110527220
|
C | T | 2 | a0001c0001t0002g0204a0001c0001t0028g0184 | 2 | HG00597.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1728-3978C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110527220 | ||||||
chr4:110527278
|
G | C | 2 | a0013c0019t0011g0285a0017c0022t0001g0158 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1728-3920G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110527278 | ||||||
chr4:110527288
|
G | A | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1728-3910G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110527288 | ||||||
chr4:110527367
|
T | C | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1728-3831T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110527367 | ||||||
chr4:110527441
|
TCAGGGAG others(22): Show |
T | 1 | a0001c0001t0001g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1728-3756_1728-372 others(33): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110527441 | ||||||
chr4:110527514
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1728-3684T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110527514 | ||||||
chr4:110527553
|
C | T | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1728-3645C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110527553 | ||||||
chr4:110527587
|
G | C | 1 | a0001c0001t0004g0189 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1728-3611G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110527587 | ||||||
chr4:110528114
|
A | G | 1 | a0001c0007t0003g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1728-3084A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528114 | ||||||
chr4:110528183
|
A | G | 1 | a0001c0001t0001g0010 | 2 | NA18962.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1728-3015A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528183 | ||||||
chr4:110528232
|
A | G | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1728-2966A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528232 | ||||||
chr4:110528291
|
G | A | 1 | a0003c0003t0004g0246 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1728-2907G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528291 | ||||||
chr4:110528358
|
A | T | 1 | a0002c0002t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1728-2840A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528358 | ||||||
chr4:110528749
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0002g0228a0007c0010t0001g0216 | 4 | HG01074.hp2 HG01433.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1728-2449G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528749 | ||||||
chr4:110528808
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1728-2390G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528808 | ||||||
chr4:110528884
|
C | A | 2 | a0002c0002t0002g0006a0002c0002t0002g0038 | 3 | HG01981.hp2 HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1728-2314C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528884 | ||||||
chr4:110528890
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0002g0078a0001c0001t0005g0145others(13): Show | 18 | HG00735.hp1 HG01975.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1728-2308G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528890 | ||||||
chr4:110528902
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0014g0230 | 4 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1728-2296A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528902 | ||||||
chr4:110528936
|
T | C | 280 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(277): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1728-2262T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528936 | ||||||
chr4:110528988
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0002g0078a0001c0001t0005g0145others(12): Show | 17 | HG00735.hp1 HG01975.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.1728-2210G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110528988 | ||||||
chr4:110529167
|
C | T | 212 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(209): Show | 234 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1728-2031C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529167 | ||||||
chr4:110529205
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1728-1993T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529205 | ||||||
chr4:110529223
|
T | C | 5 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0011others(2): Show | 6 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1728-1975T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529223 | ||||||
chr4:110529229
|
T | C | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1728-1969T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529229 | ||||||
chr4:110529316
|
T | A | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1728-1882T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529316 | ||||||
chr4:110529343
|
G | A | 20 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0001g0117others(17): Show | 23 | HG00621.hp1 HG01255.hp2 HG02602.hp1 others(20): Show |
intron_variant | MODIFIER | c.1728-1855G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529343 | ||||||
chr4:110529381
|
C | T | 212 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(209): Show | 234 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1728-1817C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529381 | ||||||
chr4:110529628
|
C | T | 2 | a0002c0002t0002g0168a0003c0003t0002g0235 | 2 | HG01255.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1728-1570C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529628 | ||||||
chr4:110529707
|
G | A | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1728-1491G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529707 | ||||||
chr4:110529790
|
G | C | 3 | a0001c0001t0002g0144a0001c0001t0027g0142a0014c0018t0013g0042 | 3 | HG02809.hp1 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1728-1408G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529790 | ||||||
chr4:110529853
|
C | T | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG00544.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1728-1345C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529853 | ||||||
chr4:110529872
|
G | A | 64 | a0001c0001t0001g0102a0001c0007t0001g0143a0001c0007t0003g0022others(61): Show | 69 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1728-1326G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529872 | ||||||
chr4:110529880
|
C | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG01981.hp1 HG02300.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1728-1318C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110529880 | ||||||
chr4:110529919
|
C | CA | 191 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(188): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1728-1272dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 110529919 | |||||
chr4:110530007
|
C | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0149a0001c0001t0002g0150others(1): Show | 6 | HG00544.hp2 HG02056.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1728-1191C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110530007 | ||||||
chr4:110530081
|
G | GA | 191 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(188): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1728-1108dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 110530081 | |||||
chr4:110530182
|
G | T | 1 | a0003c0003t0003g0283 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1728-1016G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110530182 | ||||||
chr4:110530184
|
A | G | 1 | a0002c0002t0014g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1728-1014A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110530184 | ||||||
chr4:110530360
|
G | C | 1 | a0002c0002t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1728-838G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110530360 | ||||||
chr4:110530638
|
G | A | 8 | a0001c0001t0002g0221a0004c0004t0001g0268a0004c0004t0001g0269others(5): Show | 10 | HG00673.hp1 HG02040.hp2 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.1728-560G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110530638 | ||||||
chr4:110530809
|
T | C | 2 | a0013c0019t0011g0285a0017c0022t0001g0158 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1728-389T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110530809 | ||||||
chr4:110531015
|
G | A | 276 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(273): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1728-183G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110531015 | ||||||
chr4:110531117
|
A | G | 6 | a0001c0007t0001g0143a0001c0007t0003g0022a0003c0003t0002g0282others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1728-81A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110531117 | ||||||
chr4:110531156
|
T | C | 2 | a0002c0002t0001g0105a0002c0002t0001g0106 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1728-42T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110531156 | ||||||
chr4:110531192
|
T | A | 1 | a0003c0003t0002g0279 | 1 | HG01975.hp2 | splice_region_variant&intron_variant | LOW | c.1728-6T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 10/19 | chr4 | 110531192 | ||||||
chr4:110531526
|
G | T | 16 | a0001c0001t0001g0008a0001c0001t0002g0078a0001c0001t0005g0145others(13): Show | 18 | HG00735.hp1 HG01975.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1807+249G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110531526 | ||||||
chr4:110531597
|
A | G | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1807+320A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110531597 | ||||||
chr4:110531702
|
A | C | 1 | a0001c0001t0020g0178 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1807+425A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110531702 | ||||||
chr4:110531743
|
A | G | 275 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(272): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1807+466A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110531743 | ||||||
chr4:110531772
|
C | T | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1807+495C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110531772 | ||||||
chr4:110531862
|
G | C | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1807+585G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110531862 | ||||||
chr4:110532394
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1807+1117C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110532394 | ||||||
chr4:110532504
|
G | T | 43 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0055others(40): Show | 48 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1807+1227G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110532504 | ||||||
chr4:110532559
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1807+1282T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110532559 | ||||||
chr4:110532595
|
A | G | 150 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(147): Show | 161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1807+1318A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110532595 | ||||||
chr4:110532620
|
T | TA | 4 | a0001c0001t0002g0004a0001c0001t0002g0149a0001c0001t0002g0150others(1): Show | 6 | HG00544.hp2 HG02056.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1807+1352dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110532620 | |||||
chr4:110532671
|
C | A | 97 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(94): Show | 101 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1807+1394C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110532671 | ||||||
chr4:110532708
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1807+1431C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110532708 | ||||||
chr4:110532796
|
C | A | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1807+1519C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110532796 | ||||||
chr4:110532997
|
A | G | 280 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(277): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1807+1720A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110532997 | ||||||
chr4:110533107
|
A | G | 1 | a0003c0003t0004g0281 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1807+1830A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110533107 | ||||||
chr4:110533111
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1807+1834C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110533111 | ||||||
chr4:110533420
|
CA | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(72): Show | 85 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1807+2160delA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110533420 | |||||
chr4:110533420
|
CAA | C | 59 | a0001c0001t0001g0102a0001c0001t0012g0151a0002c0002t0001g0005others(56): Show | 64 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1807+2159_1807+216 others(6): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110533420 | |||||
chr4:110533461
|
G | T | 1 | a0001c0001t0001g0197 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1807+2184G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110533461 | ||||||
chr4:110533475
|
G | A | 178 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0014others(175): Show | 201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1807+2198G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110533475 | ||||||
chr4:110533560
|
A | G | 1 | a0002c0002t0004g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1807+2283A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110533560 | ||||||
chr4:110533620
|
G | A | 280 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(277): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1807+2343G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110533620 | ||||||
chr4:110534066
|
A | G | 280 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(277): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1807+2789A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534066 | ||||||
chr4:110534213
|
TG | T | 280 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(277): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1807+2939delG | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110534213 | |||||
chr4:110534301
|
T | C | 280 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(277): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1807+3024T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534301 | ||||||
chr4:110534328
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1807+3051C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534328 | ||||||
chr4:110534403
|
A | G | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1807+3126A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534403 | ||||||
chr4:110534500
|
G | C | 280 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(277): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1807+3223G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534500 | ||||||
chr4:110534501
|
T | G | 1 | a0003c0003t0002g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1807+3224T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534501 | ||||||
chr4:110534504
|
C | CTT | 17 | a0001c0001t0002g0104a0001c0001t0002g0183a0001c0001t0002g0186others(14): Show | 17 | HG01070.hp2 HG01496.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.1807+3246_1807+324 others(6): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110534504 | |||||
chr4:110534504
|
C | CTTT | 195 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(192): Show | 217 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1807+3245_1807+324 others(7): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110534504 | |||||
chr4:110534504
|
C | CTTTT | 60 | a0001c0001t0001g0055a0001c0001t0001g0102a0001c0001t0001g0174others(57): Show | 65 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1807+3244_1807+324 others(8): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110534504 | |||||
chr4:110534504
|
C | CTTTTT | 6 | a0002c0002t0001g0081a0002c0002t0001g0091a0002c0002t0001g0223others(3): Show | 6 | HG01106.hp2 HG02293.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1807+3243_1807+324 others(9): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110534504 | |||||
chr4:110534569
|
G | A | 9 | a0002c0002t0004g0041a0002c0002t0005g0026a0002c0002t0005g0039others(6): Show | 9 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1807+3292G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534569 | ||||||
chr4:110534709
|
A | C | 86 | a0001c0001t0001g0008a0001c0001t0001g0070a0001c0001t0001g0117others(83): Show | 99 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1807+3432A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534709 | ||||||
chr4:110534789
|
A | G | 283 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(280): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1807+3512A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534789 | ||||||
chr4:110534799
|
G | A | 4 | a0002c0002t0001g0079a0005c0005t0001g0153a0005c0005t0007g0154others(1): Show | 4 | HG02486.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807+3522G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110534799 | ||||||
chr4:110535130
|
G | A | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1807+3853G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110535130 | ||||||
chr4:110535224
|
C | T | 3 | a0002c0002t0001g0090a0002c0002t0001g0092a0002c0002t0001g0093 | 3 | HG00544.hp1 NA18612.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1807+3947C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110535224 | ||||||
chr4:110535246
|
T | C | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1807+3969T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110535246 | ||||||
chr4:110535257
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1807+3980C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110535257 | ||||||
chr4:110535330
|
T | G | 1 | a0003c0003t0001g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1807+4053T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110535330 | ||||||
chr4:110535712
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1807+4435C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110535712 | ||||||
chr4:110535767
|
G | A | 55 | a0001c0001t0001g0102a0001c0001t0005g0145a0002c0002t0001g0005others(52): Show | 58 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1807+4490G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110535767 | ||||||
chr4:110535833
|
A | G | 1 | a0004c0004t0001g0233 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1807+4556A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110535833 | ||||||
chr4:110535910
|
C | G | 1 | a0003c0012t0003g0278 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1807+4633C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110535910 | ||||||
chr4:110536034
|
G | C | 6 | a0002c0002t0002g0168a0003c0003t0001g0236a0003c0003t0002g0235others(3): Show | 6 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1807+4757G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536034 | ||||||
chr4:110536039
|
G | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG02572.hp2 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807+4762G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536039 | ||||||
chr4:110536107
|
C | CA | 16 | a0001c0001t0001g0111a0001c0001t0001g0172a0001c0001t0001g0208others(13): Show | 16 | HG00597.hp1 HG00673.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1807+4856dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110536107 | |||||
chr4:110536107
|
CA | C | 51 | a0001c0001t0001g0014a0001c0001t0001g0064a0001c0001t0001g0070others(48): Show | 61 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1807+4856delA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110536107 | |||||
chr4:110536107
|
CAA | C | 80 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0056others(77): Show | 86 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1807+4855_1807+485 others(6): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110536107 | |||||
chr4:110536201
|
A | C | 1 | a0001c0001t0003g0069 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1807+4924A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536201 | ||||||
chr4:110536215
|
G | A | 1 | a0001c0001t0004g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1807+4938G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536215 | ||||||
chr4:110536253
|
G | C | 24 | a0002c0002t0001g0080a0002c0002t0001g0081a0002c0002t0001g0085others(21): Show | 25 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1807+4976G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536253 | ||||||
chr4:110536388
|
C | A | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1807+5111C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536388 | ||||||
chr4:110536397
|
C | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 7 | HG00544.hp2 HG02056.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1807+5120C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536397 | ||||||
chr4:110536574
|
T | G | 3 | a0001c0007t0001g0143a0005c0005t0007g0011a0006c0021t0001g0167 | 4 | HG02622.hp1 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807+5297T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536574 | ||||||
chr4:110536636
|
C | G | 6 | a0002c0002t0002g0168a0003c0003t0001g0236a0003c0003t0002g0235others(3): Show | 6 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1807+5359C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536636 | ||||||
chr4:110536683
|
A | G | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1807+5406A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536683 | ||||||
chr4:110536771
|
T | A | 1 | a0002c0002t0005g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1807+5494T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536771 | ||||||
chr4:110536868
|
C | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0225a0001c0001t0001g0231others(6): Show | 11 | HG02486.hp2 HG02559.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1807+5591C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110536868 | ||||||
chr4:110537093
|
G | A | 1 | a0002c0002t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1808-5658G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537093 | ||||||
chr4:110537110
|
C | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 7 | HG00544.hp2 HG02056.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1808-5641C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537110 | ||||||
chr4:110537277
|
C | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 5 | NA18942.hp2 NA18950.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1808-5474C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537277 | ||||||
chr4:110537340
|
C | T | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-5411C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537340 | ||||||
chr4:110537342
|
T | C | 4 | a0001c0001t0028g0184a0003c0003t0001g0018a0003c0003t0001g0264others(1): Show | 5 | HG00597.hp1 NA18941.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1808-5409T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537342 | ||||||
chr4:110537385
|
A | G | 1 | a0002c0002t0004g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1808-5366A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537385 | ||||||
chr4:110537454
|
A | G | 2 | a0002c0002t0002g0168a0003c0003t0002g0235 | 2 | HG01255.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1808-5297A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537454 | ||||||
chr4:110537524
|
A | G | 1 | a0008c0020t0023g0232 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1808-5227A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537524 | ||||||
chr4:110537547
|
A | T | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-5204A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537547 | ||||||
chr4:110537590
|
T | C | 1 | a0002c0002t0002g0038 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1808-5161T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537590 | ||||||
chr4:110537661
|
G | C | 149 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(146): Show | 162 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1808-5090G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537661 | ||||||
chr4:110537914
|
T | C | 22 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0002g0076others(19): Show | 27 | HG00621.hp1 HG01255.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.1808-4837T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537914 | ||||||
chr4:110537965
|
A | G | 1 | a0003c0003t0001g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1808-4786A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537965 | ||||||
chr4:110537997
|
G | A | 1 | a0002c0002t0003g0023 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1808-4754G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110537997 | ||||||
chr4:110538248
|
A | C | 4 | a0001c0001t0028g0184a0003c0003t0001g0018a0003c0003t0001g0264others(1): Show | 5 | HG00597.hp1 NA18941.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1808-4503A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110538248 | ||||||
chr4:110538393
|
C | A | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-4358C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110538393 | ||||||
chr4:110538414
|
T | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | NA18948.hp2 NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1808-4337T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110538414 | ||||||
chr4:110538600
|
G | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0055others(17): Show | 22 | HG00280.hp2 HG00735.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1808-4151G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110538600 | ||||||
chr4:110538603
|
G | A | 6 | a0002c0002t0002g0168a0003c0003t0001g0236a0003c0003t0002g0235others(3): Show | 6 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1808-4148G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110538603 | ||||||
chr4:110538622
|
A | G | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1808-4129A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110538622 | ||||||
chr4:110539234
|
G | A | 1 | a0002c0002t0001g0090 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1808-3517G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110539234 | ||||||
chr4:110539419
|
C | T | 15 | a0001c0001t0001g0008a0001c0001t0002g0078a0001c0001t0002g0139others(12): Show | 17 | HG00735.hp1 HG01975.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.1808-3332C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110539419 | ||||||
chr4:110539450
|
T | C | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1808-3301T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110539450 | ||||||
chr4:110539515
|
C | A | 1 | a0012c0009t0013g0224 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1808-3236C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110539515 | ||||||
chr4:110539617
|
T | C | 2 | a0001c0001t0005g0067a0001c0001t0011g0068 | 2 | HG01243.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1808-3134T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110539617 | ||||||
chr4:110539686
|
G | A | 2 | a0002c0002t0001g0024a0005c0005t0001g0159 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1808-3065G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110539686 | ||||||
chr4:110539745
|
A | AT | 2 | a0001c0001t0002g0221a0004c0004t0002g0020 | 3 | HG00673.hp1 NA18949.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1808-3002dupT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110539745 | |||||
chr4:110539796
|
A | G | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1808-2955A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110539796 | ||||||
chr4:110539797
|
TATC | T | 134 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(131): Show | 148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1808-2949_1808-294 others(7): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 110539797 | |||||
chr4:110539824
|
T | C | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-2927T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110539824 | ||||||
chr4:110539873
|
T | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 7 | HG00544.hp2 HG02056.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1808-2878T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110539873 | ||||||
chr4:110540091
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1808-2660G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540091 | ||||||
chr4:110540168
|
A | G | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-2583A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540168 | ||||||
chr4:110540282
|
G | A | 6 | a0002c0002t0002g0168a0003c0003t0001g0236a0003c0003t0002g0235others(3): Show | 6 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1808-2469G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540282 | ||||||
chr4:110540436
|
A | G | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-2315A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540436 | ||||||
chr4:110540547
|
A | C | 1 | a0001c0001t0002g0146 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1808-2204A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540547 | ||||||
chr4:110540616
|
C | G | 6 | a0002c0002t0002g0168a0003c0003t0001g0236a0003c0003t0002g0235others(3): Show | 6 | HG01255.hp1 HG02055.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1808-2135C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540616 | ||||||
chr4:110540766
|
C | T | 2 | a0001c0001t0009g0007a0001c0001t0009g0048 | 3 | HG00280.hp2 HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1808-1985C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540766 | ||||||
chr4:110540782
|
G | A | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1808-1969G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540782 | ||||||
chr4:110540808
|
G | A | 8 | a0002c0002t0001g0024a0002c0002t0002g0168a0003c0003t0001g0236others(5): Show | 8 | HG01255.hp1 HG02055.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1808-1943G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540808 | ||||||
chr4:110540822
|
T | C | 1 | a0002c0002t0005g0098 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1808-1929T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540822 | ||||||
chr4:110540889
|
C | T | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1808-1862C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540889 | ||||||
chr4:110540973
|
T | A | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-1778T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110540973 | ||||||
chr4:110541037
|
G | A | 1 | a0002c0002t0004g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1808-1714G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541037 | ||||||
chr4:110541042
|
G | A | 1 | a0001c0007t0003g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1808-1709G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541042 | ||||||
chr4:110541047
|
A | C | 249 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(246): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1808-1704A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541047 | ||||||
chr4:110541255
|
A | G | 1 | a0001c0001t0014g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1808-1496A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541255 | ||||||
chr4:110541429
|
A | G | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-1322A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541429 | ||||||
chr4:110541476
|
A | G | 1 | a0003c0003t0001g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1808-1275A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541476 | ||||||
chr4:110541650
|
C | T | 3 | a0002c0002t0003g0030a0002c0006t0001g0029a0002c0006t0012g0028 | 3 | HG00280.hp1 HG01256.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1808-1101C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541650 | ||||||
chr4:110541801
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0225a0001c0001t0001g0231others(6): Show | 11 | HG02486.hp2 HG02559.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1808-950A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541801 | ||||||
chr4:110541828
|
A | G | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1808-923A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541828 | ||||||
chr4:110541830
|
A | G | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-921A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541830 | ||||||
chr4:110541892
|
C | T | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1808-859C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541892 | ||||||
chr4:110541893
|
G | C | 1 | a0006c0008t0004g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1808-858G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110541893 | ||||||
chr4:110542013
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1808-738A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110542013 | ||||||
chr4:110542121
|
T | C | 141 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(138): Show | 154 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1808-630T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110542121 | ||||||
chr4:110542415
|
T | C | 6 | a0001c0001t0002g0004a0001c0001t0002g0149a0001c0001t0002g0150others(3): Show | 8 | HG00544.hp2 HG02056.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1808-336T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110542415 | ||||||
chr4:110542429
|
C | T | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-322C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110542429 | ||||||
chr4:110542457
|
G | A | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-294G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110542457 | ||||||
chr4:110542471
|
C | T | 34 | a0001c0001t0001g0102a0001c0001t0005g0145a0002c0002t0001g0005others(31): Show | 36 | HG00140.hp1 HG00642.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1808-280C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110542471 | ||||||
chr4:110542552
|
T | A | 137 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0052others(134): Show | 148 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1808-199T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110542552 | ||||||
chr4:110542557
|
C | T | 1 | a0001c0007t0003g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1808-194C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110542557 | ||||||
chr4:110542702
|
G | C | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1808-49G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 11/19 | chr4 | 110542702 | ||||||
chr4:110542991
|
A | G | 1 | a0003c0003t0001g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1945-24A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 12/19 | chr4 | 110542991 | ||||||
chr4:110543117
|
C | G | 3 | a0001c0001t0005g0180a0002c0002t0005g0044a0003c0003t0001g0275 | 3 | HG02145.hp2 HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2000+47C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543117 | ||||||
chr4:110543289
|
A | T | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2000+219A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543289 | ||||||
chr4:110543290
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2000+220A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543290 | ||||||
chr4:110543290
|
A | T | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2000+220A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543290 | ||||||
chr4:110543306
|
T | G | 4 | a0003c0003t0001g0236a0003c0003t0004g0281a0003c0003t0007g0280others(1): Show | 4 | HG02055.hp1 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2000+236T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543306 | ||||||
chr4:110543360
|
G | C | 44 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0047others(41): Show | 50 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.2000+290G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543360 | ||||||
chr4:110543727
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2000+657G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543727 | ||||||
chr4:110543756
|
T | C | 1 | a0015c0017t0002g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2000+686T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543756 | ||||||
chr4:110543762
|
C | G | 10 | a0001c0001t0005g0180a0002c0002t0001g0024a0002c0002t0002g0168others(7): Show | 10 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2000+692C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543762 | ||||||
chr4:110543762
|
C | T | 71 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(68): Show | 74 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.2000+692C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543762 | ||||||
chr4:110543802
|
G | A | 2 | a0001c0001t0005g0180a0003c0003t0001g0275 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2000+732G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543802 | ||||||
chr4:110543984
|
A | G | 1 | a0016c0011t0005g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2000+914A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110543984 | ||||||
chr4:110544100
|
A | G | 7 | a0001c0001t0001g0225a0001c0001t0014g0230a0002c0002t0001g0079others(4): Show | 8 | HG02486.hp2 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2000+1030A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110544100 | ||||||
chr4:110544123
|
A | T | 24 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0055others(21): Show | 26 | HG00280.hp1 HG00280.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.2000+1053A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110544123 | ||||||
chr4:110544202
|
C | T | 1 | a0003c0003t0002g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2000+1132C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110544202 | ||||||
chr4:110544261
|
G | T | 7 | a0001c0001t0005g0180a0002c0002t0002g0168a0003c0003t0001g0275others(4): Show | 7 | HG01255.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2000+1191G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110544261 | ||||||
chr4:110544299
|
T | A | 15 | a0002c0002t0001g0080a0002c0002t0001g0081a0002c0002t0001g0085others(12): Show | 16 | HG00597.hp2 HG01943.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.2000+1229T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110544299 | ||||||
chr4:110544730
|
T | C | 1 | a0002c0002t0001g0088 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2000+1660T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110544730 | ||||||
chr4:110544797
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2000+1727C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110544797 | ||||||
chr4:110544895
|
G | A | 1 | a0003c0012t0003g0278 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2000+1825G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110544895 | ||||||
chr4:110545007
|
A | G | 118 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0111others(115): Show | 132 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.2000+1937A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545007 | ||||||
chr4:110545447
|
C | G | 1 | a0003c0003t0002g0279 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2000+2377C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545447 | ||||||
chr4:110545518
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2000+2448G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545518 | ||||||
chr4:110545554
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2000+2484C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545554 | ||||||
chr4:110545556
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2000+2486G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545556 | ||||||
chr4:110545637
|
C | T | 1 | a0010c0016t0006g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2001-2539C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545637 | ||||||
chr4:110545641
|
C | G | 2 | a0002c0002t0001g0091a0002c0002t0001g0096 | 2 | HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2001-2535C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545641 | ||||||
chr4:110545814
|
G | A | 1 | a0003c0003t0004g0246 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2001-2362G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545814 | ||||||
chr4:110545956
|
G | A | 1 | a0004c0004t0002g0271 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2001-2220G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545956 | ||||||
chr4:110545957
|
G | T | 1 | a0001c0001t0001g0197 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2001-2219G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110545957 | ||||||
chr4:110546147
|
T | C | 12 | a0001c0001t0001g0137a0001c0001t0001g0163a0001c0001t0001g0165others(9): Show | 13 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2001-2029T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110546147 | ||||||
chr4:110546254
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0022g0124 | 3 | HG02738.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2001-1922T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110546254 | ||||||
chr4:110546303
|
T | C | 262 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(259): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.2001-1873T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110546303 | ||||||
chr4:110546312
|
C | T | 1 | a0001c0001t0003g0209 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2001-1864C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110546312 | ||||||
chr4:110546322
|
G | A | 81 | a0001c0001t0001g0116a0001c0001t0002g0004a0001c0001t0002g0061others(78): Show | 90 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.2001-1854G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110546322 | ||||||
chr4:110546334
|
C | T | 283 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(280): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.2001-1842C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110546334 | ||||||
chr4:110546483
|
A | G | 4 | a0002c0002t0002g0168a0003c0003t0002g0021a0003c0003t0002g0235others(1): Show | 5 | HG01255.hp1 HG01975.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2001-1693A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110546483 | ||||||
chr4:110546784
|
G | T | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | NA18943.hp2 NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2001-1392G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110546784 | ||||||
chr4:110547107
|
G | A | 1 | a0006c0008t0021g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2001-1069G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110547107 | ||||||
chr4:110547672
|
A | G | 254 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(251): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.2001-504A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110547672 | ||||||
chr4:110548027
|
A | G | 1 | a0006c0008t0004g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2001-149A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | chr4 | 110548027 | ||||||
chr4:110548139
|
GT | G | 34 | a0001c0001t0001g0008a0001c0001t0001g0102a0001c0001t0001g0131others(31): Show | 39 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.2001-12delT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 110548139 | |||||
chr4:110548139
|
GTT | G | 158 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(155): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2001-13_2001-12del others(2): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 110548139 | |||||
chr4:110548139
|
GTTT | G | 22 | a0001c0001t0001g0125a0001c0001t0002g0061a0001c0001t0002g0210others(19): Show | 22 | HG02027.hp1 HG02258.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.2001-14_2001-12del others(3): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 110548139 | |||||
chr4:110548139
|
GTTTT | G | 8 | a0001c0001t0001g0196a0001c0001t0002g0203a0001c0001t0014g0230others(5): Show | 8 | HG02055.hp2 HG02056.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2001-15_2001-12del others(4): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 110548139 | |||||
chr4:110548139
|
GTTTTTTT others(2): Show |
G | 27 | a0001c0001t0001g0208a0001c0001t0002g0140a0001c0001t0004g0121others(24): Show | 30 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.2001-20_2001-12del others(9): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 110548139 | |||||
chr4:110548139
|
GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0002g0149a0001c0001t0005g0179 | 2 | HG02056.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2001-21_2001-12del others(10): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 110548139 | |||||
chr4:110548139
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0027g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2001-22_2001-12del others(11): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 110548139 | |||||
chr4:110548500
|
T | C | 2 | a0001c0001t0002g0139a0002c0002t0002g0101 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2151+174T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 14/19 | chr4 | 110548500 | ||||||
chr4:110548763
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2151+437G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 14/19 | chr4 | 110548763 | ||||||
chr4:110549183
|
G | T | 1 | a0001c0001t0004g0121 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2152-163G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 14/19 | chr4 | 110549183 | ||||||
chr4:110549220
|
G | A | 2 | a0001c0001t0027g0142a0006c0008t0021g0156 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2152-126G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 14/19 | chr4 | 110549220 | ||||||
chr4:110549232
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2152-114G>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 14/19 | chr4 | 110549232 | ||||||
chr4:110549471
|
T | G | 2 | a0001c0001t0006g0075a0001c0001t0006g0126 | 2 | NA19001.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2225+52T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 15/19 | chr4 | 110549471 | ||||||
chr4:110550113
|
G | A | 63 | a0001c0001t0001g0116a0001c0001t0002g0004a0001c0001t0002g0061others(60): Show | 71 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.2501+227G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110550113 | ||||||
chr4:110550457
|
T | C | 2 | a0001c0001t0014g0230a0002c0002t0014g0100 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2501+571T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110550457 | ||||||
chr4:110550531
|
T | A | 26 | a0001c0001t0002g0140a0001c0001t0004g0121a0001c0001t0004g0127others(23): Show | 29 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2501+645T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110550531 | ||||||
chr4:110550545
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0014g0230 | 3 | HG03225.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2501+659A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110550545 | ||||||
chr4:110550575
|
C | T | 37 | a0001c0001t0002g0073a0001c0001t0002g0076a0001c0001t0002g0104others(34): Show | 42 | HG00642.hp2 HG00673.hp1 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.2501+689C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110550575 | ||||||
chr4:110550581
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2501+695T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110550581 | ||||||
chr4:110550896
|
C | G | 26 | a0001c0001t0002g0140a0001c0001t0004g0121a0001c0001t0004g0127others(23): Show | 29 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2501+1010C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110550896 | ||||||
chr4:110551019
|
C | T | 2 | a0012c0009t0013g0224a0014c0018t0013g0042 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2501+1133C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110551019 | ||||||
chr4:110551092
|
T | TA | 27 | a0001c0001t0002g0140a0001c0001t0004g0127a0001c0001t0004g0128others(24): Show | 30 | HG00642.hp1 HG00741.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2501+1225dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr4 | 110551092 | |||||
chr4:110551092
|
TA | T | 11 | a0001c0001t0001g0063a0001c0001t0001g0185a0001c0001t0002g0078others(8): Show | 11 | HG00140.hp1 HG01070.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.2501+1225delA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr4 | 110551092 | |||||
chr4:110551149
|
A | T | 1 | a0002c0002t0004g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2501+1263A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110551149 | ||||||
chr4:110551152
|
CA | C | 3 | a0001c0001t0001g0047a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG01070.hp1 HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2501+1267delA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110551152 | ||||||
chr4:110551219
|
G | A | 1 | a0001c0007t0003g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2501+1333G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110551219 | ||||||
chr4:110551678
|
A | G | 2 | a0001c0001t0030g0193a0002c0006t0012g0028 | 2 | HG00280.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2502-1637A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110551678 | ||||||
chr4:110551793
|
C | G | 19 | a0001c0001t0005g0067a0001c0001t0005g0145a0001c0001t0005g0179others(16): Show | 19 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.2502-1522C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110551793 | ||||||
chr4:110551821
|
A | G | 2 | a0001c0001t0027g0142a0006c0008t0021g0156 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2502-1494A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110551821 | ||||||
chr4:110551835
|
C | A | 1 | a0003c0003t0001g0276 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2502-1480C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110551835 | ||||||
chr4:110552082
|
T | C | 19 | a0001c0001t0005g0067a0001c0001t0005g0145a0001c0001t0005g0179others(16): Show | 19 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.2502-1233T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110552082 | ||||||
chr4:110552120
|
T | G | 1 | a0002c0002t0001g0222 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2502-1195T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110552120 | ||||||
chr4:110552210
|
G | A | 256 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(253): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.2502-1105G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110552210 | ||||||
chr4:110552239
|
AC | A | 3 | a0001c0001t0005g0179a0001c0001t0005g0180a0002c0002t0005g0044 | 3 | HG02258.hp1 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2502-1075delC | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110552239 | ||||||
chr4:110552329
|
T | G | 65 | a0001c0001t0001g0116a0001c0001t0002g0004a0001c0001t0002g0061others(62): Show | 73 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.2502-986T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110552329 | ||||||
chr4:110552629
|
G | A | 3 | a0001c0001t0004g0121a0001c0001t0004g0130a0002c0002t0004g0169 | 3 | HG00621.hp1 NA18747.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.2502-686G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110552629 | ||||||
chr4:110552665
|
T | C | 1 | a0002c0002t0001g0096 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2502-650T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110552665 | ||||||
chr4:110552693
|
T | A | 1 | a0001c0001t0001g0201 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2502-622T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110552693 | ||||||
chr4:110552751
|
T | C | 19 | a0001c0001t0005g0067a0001c0001t0005g0145a0001c0001t0005g0179others(16): Show | 19 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.2502-564T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 17/19 | chr4 | 110552751 | ||||||
chr4:110553474
|
G | A | 17 | a0001c0001t0005g0067a0001c0001t0005g0145a0001c0001t0005g0179others(14): Show | 17 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.2642+19G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110553474 | ||||||
chr4:110553503
|
C | A | 63 | a0001c0001t0001g0116a0001c0001t0002g0004a0001c0001t0002g0061others(60): Show | 71 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.2642+48C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110553503 | ||||||
chr4:110553545
|
T | G | 1 | a0002c0002t0001g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2642+90T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110553545 | ||||||
chr4:110553671
|
T | G | 1 | a0001c0001t0027g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2642+216T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110553671 | ||||||
chr4:110553855
|
A | G | 1 | a0006c0008t0021g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2642+400A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110553855 | ||||||
chr4:110554027
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2642+572C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110554027 | ||||||
chr4:110554043
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2642+588C>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110554043 | ||||||
chr4:110554264
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2642+809C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110554264 | ||||||
chr4:110554562
|
C | T | 163 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(160): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2642+1107C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110554562 | ||||||
chr4:110554608
|
G | A | 2 | a0012c0009t0013g0224a0014c0018t0013g0042 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2642+1153G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110554608 | ||||||
chr4:110554780
|
G | A | 1 | a0006c0008t0021g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2642+1325G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110554780 | ||||||
chr4:110554808
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0052a0001c0001t0001g0136others(2): Show | 6 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2642+1353A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110554808 | ||||||
chr4:110554875
|
G | A | 1 | a0002c0002t0001g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2642+1420G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110554875 | ||||||
chr4:110554954
|
G | A | 2 | a0001c0001t0001g0163a0002c0006t0001g0029 | 2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2642+1499G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110554954 | ||||||
chr4:110555019
|
T | A | 26 | a0001c0001t0002g0140a0001c0001t0004g0121a0001c0001t0004g0127others(23): Show | 29 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2642+1564T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110555019 | ||||||
chr4:110555217
|
T | C | 2 | a0001c0001t0027g0142a0006c0008t0021g0156 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2642+1762T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110555217 | ||||||
chr4:110555346
|
A | C | 26 | a0001c0001t0002g0140a0001c0001t0004g0121a0001c0001t0004g0127others(23): Show | 29 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2642+1891A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110555346 | ||||||
chr4:110555545
|
C | T | 26 | a0001c0001t0002g0140a0001c0001t0004g0121a0001c0001t0004g0127others(23): Show | 29 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2642+2090C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110555545 | ||||||
chr4:110555551
|
T | C | 1 | a0002c0002t0005g0098 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2642+2096T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110555551 | ||||||
chr4:110555757
|
T | G | 2 | a0001c0001t0027g0142a0006c0008t0021g0156 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2642+2302T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110555757 | ||||||
chr4:110555862
|
T | G | 1 | a0001c0001t0002g0191 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2642+2407T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110555862 | ||||||
chr4:110556007
|
A | T | 3 | a0001c0001t0004g0121a0001c0001t0004g0130a0002c0002t0004g0169 | 3 | HG00621.hp1 NA18747.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.2642+2552A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110556007 | ||||||
chr4:110556227
|
T | G | 3 | a0001c0001t0001g0047a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG01070.hp1 HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2642+2772T>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110556227 | ||||||
chr4:110556288
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0022g0124 | 3 | HG02738.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2642+2833C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110556288 | ||||||
chr4:110556307
|
T | A | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2642+2852T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110556307 | ||||||
chr4:110556475
|
CAATGTGT others(4): Show |
C | 64 | a0001c0001t0001g0116a0001c0001t0002g0004a0001c0001t0002g0061others(61): Show | 72 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.2642+3022_2642+303 others(15): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110556475 | |||||
chr4:110556594
|
GT | G | 26 | a0001c0001t0002g0140a0001c0001t0004g0121a0001c0001t0004g0127others(23): Show | 29 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2643-3045delT | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110556594 | |||||
chr4:110556793
|
A | G | 135 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(132): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.2643-2854A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110556793 | ||||||
chr4:110556980
|
C | G | 2 | a0001c0001t0027g0142a0006c0008t0021g0156 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2643-2667C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110556980 | ||||||
chr4:110557074
|
A | G | 3 | a0002c0002t0003g0030a0002c0002t0003g0031a0003c0003t0003g0015 | 4 | HG01256.hp1 HG01258.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2643-2573A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110557074 | ||||||
chr4:110557084
|
C | T | 2 | a0001c0001t0009g0007a0001c0001t0009g0048 | 3 | HG00280.hp2 HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2643-2563C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110557084 | ||||||
chr4:110557314
|
A | G | 1 | a0001c0001t0002g0122 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2643-2333A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110557314 | ||||||
chr4:110558032
|
A | ATTTTTTT others(1): Show |
10 | a0001c0001t0001g0176a0001c0001t0001g0211a0002c0002t0001g0086others(7): Show | 11 | HG00735.hp1 HG01070.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2643-1607_2643-160 others(12): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558032 | |||||
chr4:110558032
|
A | ATTTTTTT others(2): Show |
172 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(169): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.2643-1608_2643-160 others(13): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558032 | |||||
chr4:110558032
|
A | ATTTTTTT others(3): Show |
41 | a0001c0001t0001g0053a0001c0001t0001g0116a0001c0001t0001g0117others(38): Show | 41 | HG00544.hp1 HG01261.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.2643-1609_2643-160 others(14): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558032 | |||||
chr4:110558032
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0202a0001c0001t0027g0142a0002c0002t0001g0032others(1): Show | 4 | HG02738.hp1 HG02809.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2643-1610_2643-160 others(15): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558032 | |||||
chr4:110558032
|
A | ATTTTTTT others(5): Show |
1 | a0006c0008t0021g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2643-1611_2643-160 others(16): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558032 | |||||
chr4:110558032
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ATTTT | A | 26 | a0001c0001t0002g0140a0001c0001t0004g0121a0001c0001t0004g0127others(23): Show | 29 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2643-1603_2643-160 others(8): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558032 | |||||
chr4:110558270
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T | TTATA | 4 | a0001c0001t0006g0103a0001c0001t0014g0230a0001c0001t0027g0142others(1): Show | 4 | HG02698.hp2 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2643-1356_2643-135 others(8): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558270 | |||||
chr4:110558270
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T | TTATATAT others(1): Show |
5 | a0001c0001t0005g0067a0001c0001t0005g0179a0001c0001t0005g0180others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2643-1360_2643-135 others(12): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558270 | |||||
chr4:110558270
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T | TTATATAT others(3): Show |
7 | a0001c0001t0005g0145a0002c0002t0005g0026a0002c0002t0005g0039others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2643-1362_2643-135 others(14): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558270 | |||||
chr4:110558270
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T | TTATATAT others(5): Show |
5 | a0002c0002t0005g0040a0002c0002t0005g0049a0002c0002t0005g0050others(2): Show | 5 | HG02451.hp2 HG02965.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2643-1364_2643-135 others(16): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558270 | |||||
chr4:110558270
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T | TTATATAT others(7): Show |
1 | a0002c0002t0005g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2643-1366_2643-135 others(18): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558270 | |||||
chr4:110558270
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TTA | T | 3 | a0001c0007t0003g0022a0002c0002t0007g0099a0002c0002t0007g0109 | 3 | HG00735.hp1 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2643-1354_2643-135 others(6): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558270 | |||||
chr4:110558270
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TTATA | T | 139 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(136): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2643-1356_2643-135 others(8): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558270 | |||||
chr4:110558270
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TTATATAT others(1): Show |
T | 63 | a0001c0001t0001g0116a0001c0001t0002g0004a0001c0001t0002g0061others(60): Show | 71 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.2643-1360_2643-135 others(12): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558270 | |||||
chr4:110558291
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TATAA | T | 3 | a0001c0001t0001g0113a0002c0002t0001g0089a0002c0002t0001g0259 | 3 | NA18948.hp2 NA18977.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2643-1353_2643-135 others(8): Show |
ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110558291 | |||||
chr4:110558296
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A | T | 1 | a0001c0001t0001g0197 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2643-1351A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110558296 | ||||||
chr4:110558306
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G | T | 23 | a0001c0001t0001g0014a0001c0001t0001g0047a0001c0001t0001g0052others(20): Show | 25 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2643-1341G>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110558306 | ||||||
chr4:110558378
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C | T | 1 | a0001c0014t0029g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2643-1269C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110558378 | ||||||
chr4:110558492
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A | G | 255 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(252): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.2643-1155A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110558492 | ||||||
chr4:110558686
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T | C | 283 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(280): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.2643-961T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110558686 | ||||||
chr4:110558923
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G | A | 17 | a0001c0001t0005g0067a0001c0001t0005g0145a0001c0001t0005g0179others(14): Show | 17 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.2643-724G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110558923 | ||||||
chr4:110559069
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T | C | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG00544.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2643-578T>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110559069 | ||||||
chr4:110559104
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G | A | 1 | a0003c0003t0002g0279 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2643-543G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110559104 | ||||||
chr4:110559145
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A | G | 2 | a0001c0001t0014g0230a0002c0002t0014g0100 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2643-502A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110559145 | ||||||
chr4:110559376
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G | GA | 10 | a0001c0001t0001g0205a0001c0001t0001g0215a0001c0001t0002g0149others(7): Show | 11 | HG00609.hp1 HG00609.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.2643-259dupA | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | 110559376 | |||||
chr4:110559606
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C | T | 1 | a0001c0001t0001g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2643-41C>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 18/19 | chr4 | 110559606 | ||||||
chr4:110559764
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G | A | 24 | a0001c0001t0004g0121a0001c0001t0004g0127a0001c0001t0004g0128others(21): Show | 27 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2721+39G>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 19/19 | chr4 | 110559764 | ||||||
chr4:110559773
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A | G | 2 | a0001c0001t0014g0230a0002c0002t0014g0100 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2721+48A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 19/19 | chr4 | 110559773 | ||||||
chr4:110559781
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T | A | 1 | a0006c0008t0021g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2721+56T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 19/19 | chr4 | 110559781 | ||||||
chr4:110559782
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A | T | 1 | a0003c0003t0002g0258 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2721+57A>T | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 19/19 | chr4 | 110559782 | ||||||
chr4:110560331
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T | A | 1 | a0003c0003t0001g0242 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2721+606T>A | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 19/19 | chr4 | 110560331 | ||||||
chr4:110560604
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A | G | 1 | a0001c0001t0001g0166 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2722-802A>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 19/19 | chr4 | 110560604 | ||||||
chr4:110561114
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A | C | 1 | a0006c0008t0004g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2722-292A>C | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 19/19 | chr4 | 110561114 | ||||||
chr4:110561192
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C | G | 2 | a0001c0001t0001g0008a0001c0001t0022g0124 | 3 | HG02738.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2722-214C>G | ENPEP | ENSG00000138792.10 | transcript | ENST00000265162.10 | protein_coding | 19/19 | chr4 | 110561192 |