geneid | 8863 |
---|---|
ensemblid | ENSG00000049246.15 |
hgncid | 8847 |
symbol | PER3 |
name | period circadian regulator 3 |
refseq_nuc | NM_001377275.1 |
refseq_prot | NP_001364204.1 |
ensembl_nuc | ENST00000377532.8 |
ensembl_prot | ENSP00000366755.3 |
mane_status | MANE Select |
chr | chr1 |
start | 7784291 |
end | 7845177 |
strand | + |
ver | v1.2 |
region | chr1:7784291-7845177 |
region5000 | chr1:7779291-7850177 |
regionname0 | PER3_chr1_7784291_7845177 |
regionname5000 | PER3_chr1_7779291_7850177 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1192 | 222 | 44 | 30 | 129 | 5 | 14 | 101 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002 | 0/0 | 1210 | 96 | 34 | 14 | 32 | 4 | 12 | 26 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0003 | 0/0 | 1192 | 32 | 4 | 13 | 7 | 3 | 5 | 7 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0004 | 0/0 | 1192 | 31 | 0 | 9 | 18 | 0 | 4 | 18 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0005 | 1/1 | 1210 | 8 | 2 | 2 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0006 | 0/0 | 1192 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0007 | 0/0 | 1192 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0008 | 0/0 | 1192 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0009 | 0/0 | 1210 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0010 | 0/0 | 1192 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0011 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0012 | 0/0 | 1210 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0013 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0014 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0015 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0016 | 0/0 | 1210 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0017 | 0/0 | 1210 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0018 | 0/0 | 1210 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3579 | 107 | 23 | 11 | 60 | 1 | 12 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0002 | 0/0 | 3633 | 87 | 26 | 14 | 31 | 4 | 12 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0003 | 0/0 | 3579 | 57 | 0 | 14 | 42 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0004 | 0/0 | 3579 | 36 | 20 | 5 | 7 | 4 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0005 | 0/0 | 3579 | 32 | 4 | 13 | 7 | 3 | 5 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0006 | 0/0 | 3579 | 31 | 0 | 9 | 18 | 0 | 4 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0007 | 0/0 | 3579 | 14 | 0 | 0 | 13 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0008 | 1/1 | 3633 | 7 | 1 | 2 | 0 | 2 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0009 | 0/0 | 3579 | 4 | 3 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0010 | 0/0 | 3579 | 4 | 0 | 3 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0011 | 0/0 | 3579 | 4 | 0 | 0 | 4 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0012 | 0/0 | 3633 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0013 | 0/0 | 3633 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0014 | 0/0 | 3579 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0015 | 0/0 | 3633 | 2 | 1 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0016 | 0/0 | 3633 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0017 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0018 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0019 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0020 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0021 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0022 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0023 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0024 | 0/0 | 3633 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0025 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0026 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0027 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0028 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0029 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0030 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
c0031 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2733 | 363 | 70 | 66 | 182 | 9 | 36 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0002 | 0/0 | 2733 | 15 | 13 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0003 | 1/1 | 2733 | 7 | 1 | 2 | 0 | 2 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0004 | 0/0 | 2733 | 5 | 0 | 0 | 5 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0005 | 0/0 | 2733 | 4 | 4 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0006 | 0/0 | 2733 | 3 | 1 | 1 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0007 | 0/0 | 2733 | 2 | 0 | 0 | 0 | 2 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0008 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0009 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0010 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0011 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0012 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0013 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0014 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0015 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0016 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0017 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
t0018 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0012 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0280 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3579 | 107 | 23 | 11 | 60 | 1 | 12 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0003 | 0/0 | 3579 | 57 | 0 | 14 | 42 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0004 | 0/0 | 3579 | 36 | 20 | 5 | 7 | 4 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0007 | 0/0 | 3579 | 14 | 0 | 0 | 13 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0011 | 0/0 | 3579 | 4 | 0 | 0 | 4 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0017 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0020 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0028 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0029 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0002 | 0/0 | 3633 | 87 | 26 | 14 | 31 | 4 | 12 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0012 | 0/0 | 3633 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0013 | 0/0 | 3633 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0016 | 0/0 | 3633 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0021 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0003c0005 | 0/0 | 3579 | 32 | 4 | 13 | 7 | 3 | 5 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0004c0006 | 0/0 | 3579 | 31 | 0 | 9 | 18 | 0 | 4 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0005c0008 | 1/1 | 3633 | 7 | 1 | 2 | 0 | 2 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0005c0025 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0006c0010 | 0/0 | 3579 | 4 | 0 | 3 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0007c0009 | 0/0 | 3579 | 4 | 3 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0008c0014 | 0/0 | 3579 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0009c0015 | 0/0 | 3633 | 2 | 1 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0010c0031 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0011c0018 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0012c0024 | 0/0 | 3633 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0013c0023 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0014c0019 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0015c0022 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0016c0027 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0017c0026 | 0/0 | 3633 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0018c0030 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6311 | 103 | 22 | 11 | 57 | 1 | 12 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0001t0008 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0001t0009 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0001t0013 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0001t0018 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0003t0001 | 0/0 | 6311 | 51 | 0 | 13 | 37 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0003t0004 | 0/0 | 6311 | 5 | 0 | 0 | 5 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0003t0016 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0004t0001 | 0/0 | 6311 | 17 | 5 | 2 | 7 | 3 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0004t0002 | 0/0 | 6311 | 15 | 13 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0004t0006 | 0/0 | 6311 | 3 | 1 | 1 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0004t0011 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0007t0001 | 0/0 | 6311 | 14 | 0 | 0 | 13 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0011t0001 | 0/0 | 6311 | 4 | 0 | 0 | 4 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0017t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0020t0001 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0028t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0001c0029t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0002t0001 | 0/0 | 6365 | 86 | 25 | 14 | 31 | 4 | 12 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0002t0012 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0012t0001 | 0/0 | 6365 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0013t0001 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0013t0005 | 0/0 | 6365 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0016t0001 | 0/0 | 6365 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0002c0021t0001 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0003c0005t0001 | 0/0 | 6311 | 29 | 4 | 12 | 7 | 1 | 5 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0003c0005t0007 | 0/0 | 6311 | 2 | 0 | 0 | 0 | 2 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0003c0005t0010 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0004c0006t0001 | 0/0 | 6311 | 30 | 0 | 8 | 18 | 0 | 4 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0004c0006t0015 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0005c0008t0003 | 1/1 | 6365 | 7 | 1 | 2 | 0 | 2 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0005c0025t0014 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0006c0010t0001 | 0/0 | 6311 | 4 | 0 | 3 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0007c0009t0001 | 0/0 | 6311 | 4 | 3 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0008c0014t0001 | 0/0 | 6311 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0009c0015t0001 | 0/0 | 6365 | 2 | 1 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0010c0031t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0011c0018t0017 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0012c0024t0001 | 0/0 | 6365 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0013c0023t0001 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0014c0019t0001 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0015c0022t0005 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0016c0027t0005 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0017c0026t0001 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
a0018c0030t0001 | 0/0 | 6365 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | copy fasta | chr1 | 7779291 | 7850177 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0009g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0013g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0001t0018g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0003t0016g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0006g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0004t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0007t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0011t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0011t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0011t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0017t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0020t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0028t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0001c0029t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0002t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0012t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0012t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0012t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0013t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0013t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0013t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0016t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0016t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0002c0021t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0003c0005t0010g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0004c0006t0015g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0012 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0280 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0008t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0005c0025t0014g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0006c0010t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0006c0010t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0006c0010t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0006c0010t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0007c0009t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0007c0009t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0007c0009t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0007c0009t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0008c0014t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0008c0014t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0009c0015t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0009c0015t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0010c0031t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0011c0018t0017g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0012c0024t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0013c0023t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0014c0019t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0015c0022t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0016c0027t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0017c0026t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
a0018c0030t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0001 | g0166 | EUR | GBR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0204 | EUR | GBR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0159 | EUR | GBR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00140 | hp2 | a0005 | c0008 | t0003 | g0279 | EUR | GBR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00280 | hp1 | a0001 | c0004 | t0006 | g0156 | EUR | FIN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0210 | EUR | FIN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00423 | hp1 | a0001 | c0001 | t0009 | g0332 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00423 | hp2 | a0001 | c0007 | t0001 | g0256 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00544 | hp1 | a0001 | c0028 | t0001 | g0122 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00544 | hp2 | a0008 | c0014 | t0001 | g0386 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0387 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00621 | hp1 | a0001 | c0003 | t0004 | g0108 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00639 | hp2 | a0001 | c0004 | t0002 | g0160 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00642 | hp2 | a0004 | c0006 | t0001 | g0036 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00735 | hp1 | a0003 | c0005 | t0001 | g0079 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00735 | hp2 | a0004 | c0006 | t0015 | g0047 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00738 | hp1 | a0003 | c0005 | t0001 | g0085 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00738 | hp2 | a0004 | c0006 | t0001 | g0025 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00741 | hp1 | a0006 | c0010 | t0001 | g0133 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG00741 | hp2 | a0004 | c0006 | t0001 | g0034 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01069 | hp1 | a0004 | c0006 | t0001 | g0043 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01074 | hp1 | a0005 | c0008 | t0003 | g0278 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0129 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01106 | hp2 | a0003 | c0005 | t0001 | g0077 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01109 | hp1 | a0001 | c0004 | t0002 | g0170 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01109 | hp2 | a0004 | c0006 | t0001 | g0031 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01167 | hp1 | a0006 | c0010 | t0001 | g0124 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01167 | hp2 | a0005 | c0008 | t0003 | g0282 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0201 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01169 | hp2 | a0006 | c0010 | t0001 | g0125 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01175 | hp1 | a0003 | c0005 | t0010 | g0070 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01192 | hp2 | a0001 | c0003 | t0016 | g0115 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01243 | hp1 | a0009 | c0015 | t0001 | g0055 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01243 | hp2 | a0007 | c0009 | t0001 | g0317 | AMR | PUR | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01255 | hp2 | a0003 | c0005 | t0001 | g0076 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01256 | hp1 | a0001 | c0004 | t0001 | g0164 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0388 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0130 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0131 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01258 | hp2 | a0001 | c0004 | t0001 | g0163 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01261 | hp2 | a0001 | c0004 | t0006 | g0155 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01346 | hp1 | a0004 | c0006 | t0001 | g0040 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01346 | hp2 | a0003 | c0005 | t0001 | g0004 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0205 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01361 | hp1 | a0003 | c0005 | t0001 | g0071 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0126 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01433 | hp1 | a0003 | c0005 | t0001 | g0004 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01433 | hp2 | a0004 | c0006 | t0001 | g0026 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0142 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0240 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0329 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01516 | hp1 | a0003 | c0005 | t0007 | g0078 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0161 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01517 | hp1 | a0003 | c0005 | t0007 | g0086 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0219 | EUR | IBS | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0377 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01884 | hp2 | a0001 | c0001 | t0018 | g0375 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01891 | hp1 | a0009 | c0015 | t0001 | g0054 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01934 | hp1 | a0012 | c0024 | t0001 | g0216 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0127 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01943 | hp1 | a0001 | c0003 | t0001 | g0148 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0128 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0371 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01952 | hp2 | a0003 | c0005 | t0001 | g0069 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01975 | hp1 | a0003 | c0005 | t0001 | g0073 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0118 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01981 | hp1 | a0003 | c0005 | t0001 | g0072 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0095 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0135 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02027 | hp1 | a0001 | c0003 | t0001 | g0139 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0094 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02055 | hp1 | a0002 | c0012 | t0001 | g0179 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02055 | hp2 | a0015 | c0022 | t0005 | g0090 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02056 | hp2 | a0001 | c0007 | t0001 | g0262 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02071 | hp2 | a0001 | c0003 | t0004 | g0099 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02083 | hp1 | a0001 | c0007 | t0001 | g0257 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0383 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02135 | hp1 | a0001 | c0003 | t0004 | g0100 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02135 | hp2 | a0001 | c0017 | t0001 | g0165 | EAS | KHV | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0199 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0132 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02148 | hp2 | a0003 | c0005 | t0001 | g0087 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | CDX | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0056 | EAS | CDX | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CDX | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02165 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | CDX | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02257 | hp2 | a0013 | c0023 | t0001 | g0208 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02258 | hp2 | a0001 | c0004 | t0002 | g0173 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0277 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02280 | hp2 | a0001 | c0004 | t0002 | g0168 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02293 | hp2 | a0004 | c0006 | t0001 | g0027 | AMR | PEL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02451 | hp1 | a0001 | c0020 | t0001 | g0315 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0235 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02572 | hp1 | a0001 | c0004 | t0002 | g0001 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0275 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0223 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02615 | hp1 | a0001 | c0004 | t0002 | g0167 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02622 | hp1 | a0011 | c0018 | t0017 | g0181 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02630 | hp1 | a0001 | c0004 | t0002 | g0174 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0307 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02647 | hp1 | a0001 | c0004 | t0011 | g0058 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02647 | hp2 | a0017 | c0026 | t0001 | g0021 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02698 | hp2 | a0003 | c0005 | t0001 | g0074 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02717 | hp2 | a0002 | c0016 | t0001 | g0273 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0224 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02809 | hp2 | a0001 | c0004 | t0001 | g0308 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0270 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02886 | hp1 | a0001 | c0004 | t0002 | g0001 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02886 | hp2 | a0005 | c0025 | t0014 | g0266 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02895 | hp1 | a0002 | c0013 | t0005 | g0091 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02895 | hp2 | a0003 | c0005 | t0001 | g0005 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02897 | hp2 | a0002 | c0013 | t0005 | g0092 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02970 | hp1 | a0016 | c0027 | t0005 | g0089 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02976 | hp1 | a0003 | c0005 | t0001 | g0154 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03017 | hp2 | a0003 | c0005 | t0001 | g0176 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03041 | hp2 | a0001 | c0004 | t0002 | g0001 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03130 | hp1 | a0005 | c0008 | t0003 | g0281 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03139 | hp1 | a0002 | c0012 | t0001 | g0178 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03139 | hp2 | a0001 | c0004 | t0002 | g0169 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03195 | hp1 | a0014 | c0019 | t0001 | g0320 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03195 | hp2 | a0003 | c0005 | t0001 | g0005 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03225 | hp2 | a0007 | c0009 | t0001 | g0344 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03239 | hp2 | a0004 | c0006 | t0001 | g0030 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03453 | hp2 | a0001 | c0004 | t0002 | g0171 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03486 | hp1 | a0007 | c0009 | t0001 | g0304 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0306 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03490 | hp1 | a0004 | c0006 | t0001 | g0044 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03516 | hp2 | a0002 | c0016 | t0001 | g0182 | AFR | ESN | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03540 | hp2 | a0007 | c0009 | t0001 | g0322 | AFR | GWD | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03654 | hp1 | a0004 | c0006 | t0001 | g0028 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03688 | hp1 | a0001 | c0007 | t0001 | g0011 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0192 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03831 | hp2 | a0004 | c0006 | t0001 | g0029 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0360 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0241 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0242 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03927 | hp2 | a0006 | c0010 | t0001 | g0096 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0245 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0346 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04184 | hp1 | a0003 | c0005 | t0001 | g0080 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0367 | SAS | BEB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0250 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG04199 | hp2 | a0003 | c0005 | t0001 | g0082 | SAS | STU | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18522 | hp1 | a0001 | c0004 | t0002 | g0172 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18522 | hp2 | a0001 | c0004 | t0002 | g0008 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18612 | hp1 | a0001 | c0007 | t0001 | g0260 | EAS | CHB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18612 | hp2 | a0008 | c0014 | t0001 | g0385 | EAS | CHB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18906 | hp1 | a0002 | c0012 | t0001 | g0177 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0249 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18941 | hp2 | a0004 | c0006 | t0001 | g0037 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18944 | hp1 | a0001 | c0007 | t0001 | g0268 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18945 | hp2 | a0004 | c0006 | t0001 | g0003 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18946 | hp1 | a0001 | c0004 | t0001 | g0162 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18948 | hp2 | a0004 | c0006 | t0001 | g0048 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18949 | hp2 | a0001 | c0004 | t0001 | g0157 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18950 | hp1 | a0004 | c0006 | t0001 | g0035 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18951 | hp1 | a0004 | c0006 | t0001 | g0052 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18951 | hp2 | a0001 | c0003 | t0004 | g0102 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18952 | hp1 | a0004 | c0006 | t0001 | g0049 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18952 | hp2 | a0001 | c0007 | t0001 | g0258 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18953 | hp1 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18956 | hp1 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18956 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18959 | hp1 | a0018 | c0030 | t0001 | g0243 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18962 | hp1 | a0003 | c0005 | t0001 | g0063 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18963 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18967 | hp1 | a0001 | c0029 | t0001 | g0370 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18968 | hp2 | a0003 | c0005 | t0001 | g0081 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0093 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18969 | hp2 | a0004 | c0006 | t0001 | g0038 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18970 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18971 | hp2 | a0003 | c0005 | t0001 | g0065 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18975 | hp1 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18980 | hp2 | a0001 | c0011 | t0001 | g0330 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18982 | hp1 | a0001 | c0007 | t0001 | g0265 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18983 | hp1 | a0001 | c0007 | t0001 | g0011 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18984 | hp2 | a0001 | c0003 | t0004 | g0149 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18985 | hp2 | a0001 | c0007 | t0001 | g0203 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18986 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18987 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18989 | hp2 | a0004 | c0006 | t0001 | g0041 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18992 | hp1 | a0001 | c0003 | t0001 | g0153 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18993 | hp1 | a0004 | c0006 | t0001 | g0003 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18994 | hp2 | a0010 | c0031 | t0001 | g0019 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18997 | hp1 | a0001 | c0003 | t0001 | g0097 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18997 | hp2 | a0004 | c0006 | t0001 | g0032 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18998 | hp2 | a0004 | c0006 | t0001 | g0033 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19000 | hp1 | a0001 | c0007 | t0001 | g0255 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19002 | hp1 | a0004 | c0006 | t0001 | g0045 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19003 | hp1 | a0004 | c0006 | t0001 | g0042 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19003 | hp2 | a0001 | c0001 | t0013 | g0311 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19005 | hp1 | a0004 | c0006 | t0001 | g0050 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19010 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19011 | hp1 | a0001 | c0011 | t0001 | g0018 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0380 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19030 | hp1 | a0002 | c0002 | t0012 | g0200 | AFR | LWK | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | LWK | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19055 | hp2 | a0003 | c0005 | t0001 | g0066 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19062 | hp1 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19062 | hp2 | a0004 | c0006 | t0001 | g0051 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19063 | hp1 | a0004 | c0006 | t0001 | g0024 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0384 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19067 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19067 | hp2 | a0001 | c0007 | t0001 | g0259 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19068 | hp1 | a0004 | c0006 | t0001 | g0039 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19068 | hp2 | a0003 | c0005 | t0001 | g0067 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19070 | hp2 | a0003 | c0005 | t0001 | g0068 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19074 | hp1 | a0001 | c0011 | t0001 | g0351 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19076 | hp1 | a0002 | c0021 | t0001 | g0379 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19076 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19077 | hp1 | a0001 | c0007 | t0001 | g0261 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19077 | hp2 | a0004 | c0006 | t0001 | g0046 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19079 | hp1 | a0003 | c0005 | t0001 | g0064 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19079 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19082 | hp2 | a0001 | c0007 | t0001 | g0365 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19086 | hp1 | a0001 | c0011 | t0001 | g0018 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19240 | hp1 | a0001 | c0004 | t0002 | g0008 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | YRI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20752 | hp1 | a0003 | c0005 | t0001 | g0075 | EUR | TSI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20752 | hp2 | a0005 | c0008 | t0003 | g0012 | EUR | TSI | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20905 | hp1 | a0003 | c0005 | t0001 | g0083 | SAS | GIH | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | GIH | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG01123 | hp2 | a0003 | c0005 | t0001 | g0084 | AMR | CLM | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0274 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02486 | hp1 | a0001 | c0004 | t0006 | g0158 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02559 | hp1 | a0002 | c0013 | t0001 | g0088 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0236 | AFR | ACB | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03471 | hp1 | a0001 | c0004 | t0002 | g0175 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | USA | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
HG06807 | hp2 | a0003 | c0005 | t0001 | g0057 | AFR | USA | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | USA | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | USA | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | LWK | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | LWK | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
homoSapiens_chm13v2 | hp1 | a0005 | c0008 | t0003 | g0012 | REF | REF | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
homoSapiens_grch38 | hp1 | a0005 | c0008 | t0003 | g0280 | REF | REF | PER3_chr1_7779291_7850177 | PER3 | chr1 | 7779291 | 7850177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:7785533
|
C | T | 1 | a0010 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.221C>T | p.Pro74Leu | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/22 | 531/6365 | 221/3633 | 74/1210 | chr1 | 7785533 | ||
chr1:7788142
|
C | T | 1 | a0018 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.488C>T | p.Ala163Val | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/22 | 798/6365 | 488/3633 | 163/1210 | chr1 | 7788142 | ||
chr1:7809908
|
G | A | 1 | a0011 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1258G>A | p.Val420Met | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/22 | 1568/6365 | 1258/3633 | 420/1210 | chr1 | 7809908 | ||
chr1:7820620
|
A | G | 1 | a0017 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1937A>G | p.His646Arg | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/22 | 2247/6365 | 1937/3633 | 646/1210 | chr1 | 7820620 | ||
chr1:7820623
|
T | G | 1 | a0003 | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
missense_variant | MODERATE | c.1940T>G | p.Val647Gly | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/22 | 2250/6365 | 1940/3633 | 647/1210 | chr1 | 7820623 | ||
chr1:7827174
|
C | T | 1 | a0016 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.2245C>T | p.Arg749Trp | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2555/6365 | 2245/3633 | 749/1210 | chr1 | 7827174 | ||
chr1:7827202
|
G | A | 1 | a0006 | 4 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
missense_variant | MODERATE | c.2273G>A | p.Ser758Asn | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2583/6365 | 2273/3633 | 758/1210 | chr1 | 7827202 | ||
chr1:7827433
|
T | C | 17 | a0001a0002a0003others(14): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
missense_variant | MODERATE | c.2504T>C | p.Leu835Pro | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2814/6365 | 2504/3633 | 835/1210 | chr1 | 7827433 | ||
chr1:7827439
|
T | G | 1 | a0009 | 2 | HG01243.hp1 HG01891.hp1 |
missense_variant | MODERATE | c.2510T>G | p.Leu837Trp | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2820/6365 | 2510/3633 | 837/1210 | chr1 | 7827439 | ||
chr1:7827519
|
C | G | 1 | a0004 | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
missense_variant | MODERATE | c.2590C>G | p.Pro864Ala | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2900/6365 | 2590/3633 | 864/1210 | chr1 | 7827519 | ||
chr1:7827709
|
C | T | 1 | a0008 | 2 | HG00544.hp2 NA18612.hp2 |
missense_variant | MODERATE | c.2780C>T | p.Ser927Leu | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 3090/6365 | 2780/3633 | 927/1210 | chr1 | 7827709 | ||
chr1:7829912
|
GAGAATCC others(47): Show |
G | 10 | a0001a0003a0004others(7): Show | 299 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(296): Show |
conservative_inframe_deletion | MODERATE | c.3046_3099delGCTCTG others(48): Show |
p.Ala1016_Ser1033del | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3356/6365 | 3046/3633 | 1016/1210 | INFO_REALIGN_3_PRIME | chr1 | 7829912 | |
chr1:7830003
|
CAGGATCG others(47): Show |
C | 1 | a0013 | 1 | HG02257.hp2 | disruptive_inframe_deletion | MODERATE | c.3057_3110delAGGATC others(48): Show |
p.Gly1020_Met1037del | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3367/6365 | 3057/3633 | 1019/1210 | chr1 | 7830003 | ||
chr1:7830057
|
T | C | 3 | a0003a0004a0015 | 64 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(61): Show |
missense_variant | MODERATE | c.3110T>C | p.Met1037Thr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3420/6365 | 3110/3633 | 1037/1210 | chr1 | 7830057 | ||
chr1:7830063
|
T | C | 1 | a0013 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.3116T>C | p.Leu1039Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3426/6365 | 3116/3633 | 1039/1210 | chr1 | 7830063 | ||
chr1:7835781
|
A | G | 1 | a0014 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.3234A>G | p.Ile1078Met | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/22 | 3544/6365 | 3234/3633 | 1078/1210 | chr1 | 7835781 | ||
chr1:7835906
|
C | T | 1 | a0012 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.3359C>T | p.Thr1120Ile | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/22 | 3669/6365 | 3359/3633 | 1120/1210 | chr1 | 7835906 | ||
chr1:7837073
|
A | G | 1 | a0003 | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
missense_variant | MODERATE | c.3473A>G | p.His1158Arg | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/22 | 3783/6365 | 3473/3633 | 1158/1210 | chr1 | 7837073 | ||
chr1:7842676
|
G | C | 1 | a0007 | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.3554G>C | p.Cys1185Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 3864/6365 | 3554/3633 | 1185/1210 | chr1 | 7842676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:7785468
|
T | G | 1 | a0001c0017 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.156T>G | p.Ser52Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/22 | 466/6365 | 156/3633 | 52/1210 | chr1 | 7785468 | ||
chr1:7785507
|
C | T | 1 | a0001c0011 | 4 | NA18980.hp2 NA19011.hp1 NA19074.hp1 others(1): Show |
synonymous_variant | LOW | c.195C>T | p.Tyr65Tyr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/22 | 505/6365 | 195/3633 | 65/1210 | chr1 | 7785507 | ||
chr1:7794006
|
C | T | 1 | a0001c0029 | 1 | NA18967.hp1 | splice_region_variant&synonymous_variant | LOW | c.642C>T | p.Ile214Ile | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/22 | 952/6365 | 642/3633 | 214/1210 | chr1 | 7794006 | ||
chr1:7809988
|
T | C | 27 | a0001c0001a0001c0004a0001c0007others(24): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.1338T>C | p.Ser446Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/22 | 1648/6365 | 1338/3633 | 446/1210 | chr1 | 7809988 | ||
chr1:7820525
|
A | T | 2 | a0002c0013a0016c0027 | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.1842A>T | p.Ile614Ile | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/22 | 2152/6365 | 1842/3633 | 614/1210 | chr1 | 7820525 | ||
chr1:7827188
|
G | A | 16 | a0001c0001a0001c0003a0001c0004others(13): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
synonymous_variant | LOW | c.2259G>A | p.Pro753Pro | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2569/6365 | 2259/3633 | 753/1210 | chr1 | 7827188 | ||
chr1:7827344
|
C | T | 1 | a0001c0007 | 14 | HG00423.hp2 HG02056.hp2 HG02083.hp1 others(11): Show |
synonymous_variant | LOW | c.2415C>T | p.Tyr805Tyr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2725/6365 | 2415/3633 | 805/1210 | chr1 | 7827344 | ||
chr1:7827413
|
A | G | 1 | a0001c0028 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.2484A>G | p.Ala828Ala | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2794/6365 | 2484/3633 | 828/1210 | chr1 | 7827413 | ||
chr1:7827545
|
G | A | 3 | a0001c0003a0001c0028a0006c0010 | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
synonymous_variant | LOW | c.2616G>A | p.Ser872Ser | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/22 | 2926/6365 | 2616/3633 | 872/1210 | chr1 | 7827545 | ||
chr1:7829881
|
C | T | 10 | a0001c0001a0001c0007a0001c0011others(7): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
synonymous_variant | LOW | c.2934C>T | p.Thr978Thr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3244/6365 | 2934/3633 | 978/1210 | chr1 | 7829881 | ||
chr1:7829887
|
A | G | 1 | a0002c0012 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.2940A>G | p.Ala980Ala | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3250/6365 | 2940/3633 | 980/1210 | chr1 | 7829887 | ||
chr1:7830004
|
A | G | 6 | a0002c0002a0005c0025a0009c0015others(3): Show | 93 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
synonymous_variant | LOW | c.3057A>G | p.Thr1019Thr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3367/6365 | 3057/3633 | 1019/1210 | chr1 | 7830004 | ||
chr1:7830112
|
G | T | 1 | a0001c0020 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.3165G>T | p.Thr1055Thr | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/22 | 3475/6365 | 3165/3633 | 1055/1210 | chr1 | 7830112 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:7784731
|
C | T | 1 | a0001c0001t0018 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/22 | 147 | chr1 | 7784731 | |||||
chr1:7784740
|
C | T | 1 | a0011c0018t0017 | 1 | HG02622.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-138C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/22 | chr1 | 7784740 | ||||||
chr1:7784794
|
G | A | 3 | a0002c0013t0005a0015c0022t0005a0016c0027t0005 | 4 | HG02055.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-84G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/22 | 84 | chr1 | 7784794 | |||||
chr1:7842793
|
C | T | 1 | a0001c0003t0016 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*38C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 38 | chr1 | 7842793 | |||||
chr1:7843186
|
A | G | 1 | a0004c0006t0015 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*431A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 431 | chr1 | 7843186 | |||||
chr1:7843511
|
C | T | 1 | a0005c0025t0014 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 756 | chr1 | 7843511 | |||||
chr1:7843534
|
A | T | 1 | a0001c0001t0013 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*779A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 779 | chr1 | 7843534 | |||||
chr1:7843778
|
G | A | 1 | a0001c0004t0002 | 15 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1023G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1023 | chr1 | 7843778 | |||||
chr1:7844069
|
G | T | 1 | a0002c0002t0012 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1314 | chr1 | 7844069 | |||||
chr1:7844123
|
C | T | 1 | a0001c0004t0011 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1368C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1368 | chr1 | 7844123 | |||||
chr1:7844136
|
A | G | 1 | a0003c0005t0010 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1381A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1381 | chr1 | 7844136 | |||||
chr1:7844175
|
C | T | 1 | a0001c0003t0004 | 5 | HG00621.hp1 HG02071.hp2 HG02135.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1420C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1420 | chr1 | 7844175 | |||||
chr1:7844187
|
C | T | 44 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(41): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
3_prime_UTR_variant | MODIFIER | c.*1432C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1432 | chr1 | 7844187 | |||||
chr1:7844415
|
G | A | 44 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(41): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
3_prime_UTR_variant | MODIFIER | c.*1660G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1660 | chr1 | 7844415 | |||||
chr1:7844639
|
C | T | 1 | a0001c0004t0006 | 3 | HG00280.hp1 HG01261.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1884C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 1884 | chr1 | 7844639 | |||||
chr1:7844820
|
C | T | 1 | a0005c0025t0014 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2065C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 2065 | chr1 | 7844820 | |||||
chr1:7844920
|
G | T | 1 | a0003c0005t0007 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2165G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 2165 | chr1 | 7844920 | |||||
chr1:7845050
|
C | T | 1 | a0001c0001t0009 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 2295 | chr1 | 7845050 | |||||
chr1:7845161
|
G | A | 1 | a0001c0001t0008 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2406G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 22/22 | 2406 | chr1 | 7845161 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:7784381
|
GTGCGCGG others(14): Show |
G | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG00673.hp2 HG01070.hp1 |
splice_region_variant&intron_variant | LOW | c.-225+8_-225+28delC others(20): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 7784381 | |||||
chr1:7784383
|
G | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(112): Show | 123 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(120): Show |
splice_region_variant&intron_variant | LOW | c.-225+7G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784383 | ||||||
chr1:7784384
|
C | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(112): Show | 123 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(120): Show |
splice_region_variant&intron_variant | LOW | c.-225+8C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784384 | ||||||
chr1:7784384
|
CGCGGCCG others(14): Show |
C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0017c0026t0001g0021 | 3 | HG02647.hp2 NA18989.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-225+32_-225+52del others(21): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 7784384 | |||||
chr1:7784404
|
G | T | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG00673.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.-225+28G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784404 | ||||||
chr1:7784405
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG00673.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.-225+29G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784405 | ||||||
chr1:7784409
|
G | A | 30 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(27): Show | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-225+33G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784409 | ||||||
chr1:7784471
|
A | C | 1 | a0001c0001t0001g0388 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-225+95A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784471 | ||||||
chr1:7784620
|
T | C | 267 | a0001c0001t0001g0180a0001c0001t0001g0263a0001c0001t0001g0264others(264): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-224-34T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784620 | ||||||
chr1:7784648
|
C | T | 2 | a0005c0008t0003g0281a0005c0008t0003g0282 | 2 | HG01167.hp2 HG03130.hp1 |
splice_region_variant&intron_variant | LOW | c.-224-6C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 1/21 | chr1 | 7784648 | ||||||
chr1:7785027
|
G | A | 19 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(16): Show | 19 | HG00438.hp2 HG00558.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.128+22G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785027 | ||||||
chr1:7785157
|
G | A | 1 | a0002c0002t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.128+152G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785157 | ||||||
chr1:7785312
|
G | T | 1 | a0001c0001t0001g0387 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.129-129G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785312 | ||||||
chr1:7785333
|
T | C | 2 | a0009c0015t0001g0054a0009c0015t0001g0055 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.129-108T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785333 | ||||||
chr1:7785353
|
A | G | 1 | a0002c0002t0001g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.129-88A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 2/21 | chr1 | 7785353 | ||||||
chr1:7785635
|
T | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(280): Show | 299 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.274+49T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785635 | ||||||
chr1:7785686
|
G | C | 4 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187others(1): Show | 4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+100G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785686 | ||||||
chr1:7785716
|
G | A | 1 | a0004c0006t0001g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.274+130G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785716 | ||||||
chr1:7785725
|
C | T | 2 | a0002c0002t0001g0183a0002c0002t0001g0184 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.274+139C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785725 | ||||||
chr1:7785765
|
A | T | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.274+179A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785765 | ||||||
chr1:7785890
|
T | G | 1 | a0001c0004t0001g0056 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.274+304T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785890 | ||||||
chr1:7785986
|
G | A | 2 | a0002c0002t0001g0009a0002c0002t0001g0188 | 3 | HG00733.hp1 HG01168.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.274+400G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7785986 | ||||||
chr1:7786005
|
C | G | 1 | a0001c0001t0001g0301 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.274+419C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786005 | ||||||
chr1:7786032
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.274+446A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786032 | ||||||
chr1:7786086
|
C | T | 61 | a0001c0003t0001g0093a0001c0003t0001g0094a0001c0003t0001g0095others(58): Show | 61 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.274+500C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786086 | ||||||
chr1:7786197
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.275-524G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786197 | ||||||
chr1:7786209
|
C | T | 5 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(2): Show | 5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-512C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786209 | ||||||
chr1:7786210
|
A | G | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.275-511A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786210 | ||||||
chr1:7786225
|
C | A | 1 | a0007c0009t0001g0304 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.275-496C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786225 | ||||||
chr1:7786241
|
C | T | 1 | a0002c0002t0001g0276 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.275-480C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786241 | ||||||
chr1:7786246
|
C | G | 26 | a0003c0005t0001g0004a0003c0005t0001g0063a0003c0005t0001g0064others(23): Show | 27 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.275-475C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786246 | ||||||
chr1:7786247
|
T | A | 26 | a0003c0005t0001g0004a0003c0005t0001g0063a0003c0005t0001g0064others(23): Show | 27 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.275-474T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786247 | ||||||
chr1:7786285
|
T | C | 4 | a0003c0005t0001g0005a0003c0005t0001g0154a0009c0015t0001g0054others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-436T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786285 | ||||||
chr1:7786447
|
C | T | 3 | a0001c0001t0001g0299a0001c0001t0001g0300a0002c0016t0001g0182 | 3 | HG03209.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.275-274C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786447 | ||||||
chr1:7786467
|
A | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.275-254A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786467 | ||||||
chr1:7786477
|
TTTAG | T | 30 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(27): Show | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.275-238_275-235del others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 7786477 | |||||
chr1:7786658
|
G | A | 1 | a0003c0005t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.275-63G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786658 | ||||||
chr1:7786659
|
A | G | 1 | a0003c0005t0001g0087 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.275-62A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 3/21 | chr1 | 7786659 | ||||||
chr1:7786940
|
A | G | 4 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0274others(1): Show | 5 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+104A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7786940 | ||||||
chr1:7787003
|
A | G | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.390+167A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787003 | ||||||
chr1:7787072
|
G | A | 1 | a0002c0002t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+236G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787072 | ||||||
chr1:7787165
|
C | T | 19 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(16): Show | 19 | HG00438.hp2 HG00558.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.390+329C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787165 | ||||||
chr1:7787166
|
G | A | 15 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(12): Show | 16 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.390+330G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787166 | ||||||
chr1:7787302
|
C | CT | 376 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(373): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.390+472dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 7787302 | |||||
chr1:7787355
|
C | T | 1 | a0011c0018t0017g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.390+519C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787355 | ||||||
chr1:7787420
|
C | T | 2 | a0002c0002t0001g0271a0002c0002t0001g0272 | 2 | NA18957.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.390+584C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787420 | ||||||
chr1:7787469
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(115): Show | 126 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.391-576A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787469 | ||||||
chr1:7787471
|
A | G | 1 | a0001c0003t0001g0153 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.391-574A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787471 | ||||||
chr1:7787554
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(146): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.391-491G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787554 | ||||||
chr1:7787640
|
A | T | 4 | a0003c0005t0001g0005a0003c0005t0001g0154a0009c0015t0001g0054others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-405A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787640 | ||||||
chr1:7787707
|
G | A | 1 | a0002c0002t0001g0202 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.391-338G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787707 | ||||||
chr1:7787776
|
T | C | 226 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0003t0001g0062others(223): Show | 231 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.391-269T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787776 | ||||||
chr1:7787786
|
G | A | 26 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(23): Show | 31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.391-259G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787786 | ||||||
chr1:7787903
|
G | C | 4 | a0003c0005t0001g0005a0003c0005t0001g0154a0009c0015t0001g0054others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-142G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 4/21 | chr1 | 7787903 | ||||||
chr1:7788273
|
A | G | 2 | a0002c0002t0001g0269a0002c0002t0001g0270 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.592+27A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788273 | ||||||
chr1:7788350
|
A | G | 1 | a0004c0006t0001g0052 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.592+104A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788350 | ||||||
chr1:7788372
|
T | C | 1 | a0001c0007t0001g0203 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.592+126T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788372 | ||||||
chr1:7788497
|
G | A | 84 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0007t0001g0011others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.592+251G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788497 | ||||||
chr1:7788527
|
G | C | 1 | a0002c0013t0001g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.592+281G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788527 | ||||||
chr1:7788551
|
T | G | 3 | a0002c0002t0001g0204a0002c0002t0001g0205a0002c0002t0001g0206 | 3 | HG00099.hp2 HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.592+305T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788551 | ||||||
chr1:7788556
|
GT | G | 65 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179others(62): Show | 67 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.592+315delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788556 | |||||
chr1:7788632
|
G | A | 27 | a0003c0005t0001g0004a0003c0005t0001g0057a0003c0005t0001g0063others(24): Show | 28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.592+386G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788632 | ||||||
chr1:7788664
|
G | T | 1 | a0001c0001t0001g0384 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.592+418G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788664 | ||||||
chr1:7788740
|
C | T | 1 | a0001c0003t0001g0152 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.592+494C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788740 | ||||||
chr1:7788768
|
G | A | 27 | a0003c0005t0001g0004a0003c0005t0001g0057a0003c0005t0001g0063others(24): Show | 28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.592+522G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788768 | ||||||
chr1:7788863
|
C | A | 1 | a0001c0001t0001g0384 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.592+617C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788863 | ||||||
chr1:7788883
|
G | A | 30 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(27): Show | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+637G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788883 | ||||||
chr1:7788903
|
T | TG | 5 | a0001c0001t0001g0380a0001c0001t0001g0381a0001c0001t0001g0382others(2): Show | 5 | HG02129.hp2 NA19007.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+661dupG | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788903 | |||||
chr1:7788907
|
G | GA | 129 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(126): Show | 137 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.592+678dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788907 | |||||
chr1:7788907
|
G | GAA | 10 | a0001c0001t0001g0305a0001c0003t0001g0150a0001c0003t0001g0153others(7): Show | 10 | NA18948.hp1 NA18962.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.592+677_592+678dup others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788907 | |||||
chr1:7788907
|
G | GAAA | 58 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(55): Show | 58 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.592+676_592+678dup others(3): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788907 | |||||
chr1:7788907
|
GA | G | 98 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0007t0001g0011others(95): Show | 101 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.592+678delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788907 | |||||
chr1:7788924
|
A | AT | 30 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179others(27): Show | 31 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.592+680dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788924 | |||||
chr1:7788924
|
A | T | 2 | a0004c0006t0001g0050a0004c0006t0001g0051 | 2 | NA19005.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.592+678A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7788924 | ||||||
chr1:7788940
|
CTCTTACA others(5): Show |
C | 1 | a0002c0002t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.592+699_592+710del others(12): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7788940 | |||||
chr1:7789140
|
A | AAT | 121 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(118): Show | 128 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.592+911_592+912dup others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | |||||
chr1:7789140
|
A | AATAT | 3 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0003t0001g0093 | 3 | HG02165.hp1 HG03831.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.592+909_592+912dup others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | |||||
chr1:7789140
|
A | AATATAT | 12 | a0001c0004t0001g0013a0001c0004t0001g0308a0001c0004t0011g0058others(9): Show | 14 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.592+907_592+912dup others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | |||||
chr1:7789140
|
A | AATATATA others(1): Show |
12 | a0001c0004t0001g0306a0001c0004t0001g0307a0001c0004t0002g0001others(9): Show | 15 | HG01109.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.592+905_592+912dup others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | |||||
chr1:7789140
|
A | AATATATA others(3): Show |
11 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0161others(8): Show | 13 | HG00099.hp1 HG00639.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.592+903_592+912dup others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | |||||
chr1:7789140
|
A | AATATATA others(5): Show |
4 | a0001c0004t0001g0056a0001c0004t0001g0157a0001c0004t0001g0159others(1): Show | 4 | HG00140.hp1 HG02155.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+901_592+912dup others(12): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | |||||
chr1:7789140
|
A | AATATATA others(7): Show |
2 | a0001c0004t0006g0155a0001c0004t0006g0156 | 2 | HG00280.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.592+899_592+912dup others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789140 | |||||
chr1:7789145
|
A | ATG | 101 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0007t0001g0011others(98): Show | 104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.592+900_592+901ins others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789145 | |||||
chr1:7789145
|
A | G | 1 | a0004c0006t0001g0049 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.592+899A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789145 | ||||||
chr1:7789163
|
G | A | 3 | a0002c0012t0001g0177a0005c0008t0003g0281a0005c0008t0003g0282 | 3 | HG01167.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.592+917G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789163 | ||||||
chr1:7789195
|
TA | T | 33 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179others(30): Show | 34 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.592+959delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789195 | |||||
chr1:7789435
|
T | G | 1 | a0001c0004t0001g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.592+1189T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789435 | ||||||
chr1:7789452
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.592+1206C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789452 | ||||||
chr1:7789494
|
G | A | 1 | a0002c0012t0001g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.592+1248G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789494 | ||||||
chr1:7789596
|
A | G | 106 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0007t0001g0011others(103): Show | 109 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.592+1350A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789596 | ||||||
chr1:7789598
|
C | A | 4 | a0002c0013t0005g0091a0002c0013t0005g0092a0015c0022t0005g0090others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+1352C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789598 | ||||||
chr1:7789722
|
T | G | 1 | a0001c0001t0001g0384 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.592+1476T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789722 | ||||||
chr1:7789768
|
C | G | 1 | a0001c0001t0001g0384 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.592+1522C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789768 | ||||||
chr1:7789781
|
C | T | 23 | a0001c0001t0001g0284a0001c0001t0001g0358a0001c0001t0001g0359others(20): Show | 23 | HG00673.hp2 HG01952.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+1535C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789781 | ||||||
chr1:7789820
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(112): Show | 122 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.592+1574A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7789820 | ||||||
chr1:7789840
|
ATGTCATC others(6): Show |
A | 1 | a0001c0004t0002g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.592+1597_592+1609d others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7789840 | |||||
chr1:7790002
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(147): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.592+1756C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790002 | ||||||
chr1:7790021
|
C | T | 101 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0007t0001g0011others(98): Show | 104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.592+1775C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790021 | ||||||
chr1:7790107
|
C | T | 1 | a0001c0007t0001g0268 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.592+1861C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790107 | ||||||
chr1:7790111
|
G | A | 1 | a0003c0005t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+1865G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790111 | ||||||
chr1:7790158
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(147): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.592+1912C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790158 | ||||||
chr1:7790166
|
C | T | 1 | a0001c0003t0001g0151 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.592+1920C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790166 | ||||||
chr1:7790359
|
G | A | 1 | a0002c0021t0001g0379 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.592+2113G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790359 | ||||||
chr1:7790405
|
C | T | 1 | a0002c0016t0001g0273 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.592+2159C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790405 | ||||||
chr1:7790463
|
C | T | 2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | NA18982.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.592+2217C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790463 | ||||||
chr1:7790540
|
A | G | 4 | a0003c0005t0001g0005a0003c0005t0001g0154a0009c0015t0001g0054others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+2294A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790540 | ||||||
chr1:7790561
|
C | G | 2 | a0003c0005t0001g0005a0003c0005t0001g0154 | 3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.592+2315C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790561 | ||||||
chr1:7790750
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.592+2504C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790750 | ||||||
chr1:7790794
|
T | A | 1 | a0002c0002t0001g0207 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.592+2548T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790794 | ||||||
chr1:7790798
|
CA | C | 4 | a0003c0005t0001g0005a0003c0005t0001g0154a0009c0015t0001g0054others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+2556delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7790798 | |||||
chr1:7790830
|
C | T | 1 | a0002c0002t0012g0200 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.592+2584C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790830 | ||||||
chr1:7790838
|
C | T | 26 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(23): Show | 31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.592+2592C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7790838 | ||||||
chr1:7791033
|
C | T | 101 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0007t0001g0011others(98): Show | 104 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.592+2787C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791033 | ||||||
chr1:7791138
|
C | T | 1 | a0001c0001t0001g0373 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.593-2819C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791138 | ||||||
chr1:7791198
|
CT | C | 26 | a0003c0005t0001g0004a0003c0005t0001g0063a0003c0005t0001g0064others(23): Show | 27 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.593-2758delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791198 | ||||||
chr1:7791332
|
G | A | 1 | a0011c0018t0017g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.593-2625G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791332 | ||||||
chr1:7791407
|
G | A | 1 | a0001c0003t0001g0095 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.593-2550G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791407 | ||||||
chr1:7791485
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0312a0001c0001t0001g0313others(5): Show | 9 | HG00558.hp1 HG02080.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.593-2472G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791485 | ||||||
chr1:7791577
|
C | T | 61 | a0001c0003t0001g0093a0001c0003t0001g0094a0001c0003t0001g0095others(58): Show | 61 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.593-2380C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791577 | ||||||
chr1:7791594
|
A | C | 5 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(2): Show | 5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-2363A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791594 | ||||||
chr1:7791680
|
T | C | 1 | a0006c0010t0001g0096 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.593-2277T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791680 | ||||||
chr1:7791748
|
C | T | 1 | a0001c0001t0001g0354 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.593-2209C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791748 | ||||||
chr1:7791792
|
G | A | 1 | a0013c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.593-2165G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791792 | ||||||
chr1:7791860
|
G | C | 1 | a0001c0001t0001g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.593-2097G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791860 | ||||||
chr1:7791993
|
A | C | 1 | a0001c0003t0001g0148 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.593-1964A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7791993 | ||||||
chr1:7792057
|
C | G | 30 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(27): Show | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-1900C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792057 | ||||||
chr1:7792069
|
T | C | 27 | a0003c0005t0001g0004a0003c0005t0001g0057a0003c0005t0001g0063others(24): Show | 28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1888T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792069 | ||||||
chr1:7792132
|
T | C | 1 | a0002c0002t0001g0209 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.593-1825T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792132 | ||||||
chr1:7792299
|
AACTC | A | 6 | a0004c0006t0001g0026a0004c0006t0001g0027a0004c0006t0001g0028others(3): Show | 6 | HG01109.hp2 HG01433.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.593-1654_593-1651d others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 7792299 | |||||
chr1:7792311
|
C | T | 15 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(12): Show | 16 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.593-1646C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792311 | ||||||
chr1:7792330
|
A | G | 1 | a0002c0002t0001g0267 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.593-1627A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792330 | ||||||
chr1:7792375
|
CAT | C | 6 | a0001c0004t0002g0008a0001c0004t0002g0173a0001c0004t0002g0174others(3): Show | 7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-1581_593-1580d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792375 | ||||||
chr1:7792417
|
G | A | 15 | a0001c0003t0001g0097a0001c0003t0001g0098a0001c0003t0001g0101others(12): Show | 15 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.593-1540G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792417 | ||||||
chr1:7792507
|
A | G | 5 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(2): Show | 5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-1450A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792507 | ||||||
chr1:7792517
|
A | G | 1 | a0004c0006t0001g0048 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.593-1440A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792517 | ||||||
chr1:7792630
|
C | G | 1 | a0001c0001t0001g0310 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.593-1327C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792630 | ||||||
chr1:7792705
|
C | T | 1 | a0002c0002t0001g0267 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.593-1252C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792705 | ||||||
chr1:7792737
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(147): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.593-1220C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792737 | ||||||
chr1:7792851
|
G | A | 4 | a0003c0005t0001g0005a0003c0005t0001g0154a0009c0015t0001g0054others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1106G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792851 | ||||||
chr1:7792859
|
T | C | 27 | a0003c0005t0001g0004a0003c0005t0001g0057a0003c0005t0001g0063others(24): Show | 28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1098T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792859 | ||||||
chr1:7792919
|
T | G | 2 | a0004c0006t0001g0032a0004c0006t0001g0033 | 2 | NA18997.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.593-1038T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7792919 | ||||||
chr1:7793089
|
T | G | 1 | a0001c0020t0001g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.593-868T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793089 | ||||||
chr1:7793143
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.593-814C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793143 | ||||||
chr1:7793532
|
T | C | 68 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(65): Show | 68 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.593-425T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793532 | ||||||
chr1:7793540
|
C | G | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.593-417C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793540 | ||||||
chr1:7793659
|
C | G | 1 | a0004c0006t0015g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.593-298C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793659 | ||||||
chr1:7793692
|
T | C | 1 | a0016c0027t0005g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.593-265T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793692 | ||||||
chr1:7793695
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.593-262G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793695 | ||||||
chr1:7793752
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.593-205G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793752 | ||||||
chr1:7793780
|
T | A | 1 | a0013c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.593-177T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 5/21 | chr1 | 7793780 | ||||||
chr1:7794105
|
T | A | 5 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(2): Show | 5 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+97T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794105 | ||||||
chr1:7794145
|
A | G | 1 | a0004c0006t0001g0031 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.644+137A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794145 | ||||||
chr1:7794149
|
C | T | 27 | a0003c0005t0001g0004a0003c0005t0001g0057a0003c0005t0001g0063others(24): Show | 28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.644+141C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794149 | ||||||
chr1:7794270
|
G | A | 15 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(12): Show | 16 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.644+262G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794270 | ||||||
chr1:7794290
|
C | A | 1 | a0001c0001t0001g0380 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.644+282C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794290 | ||||||
chr1:7794391
|
G | A | 1 | a0007c0009t0001g0317 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.644+383G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794391 | ||||||
chr1:7794479
|
G | A | 4 | a0002c0002t0001g0059a0002c0002t0001g0060a0002c0002t0001g0183others(1): Show | 4 | HG02717.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+471G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794479 | ||||||
chr1:7794495
|
A | G | 38 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179others(35): Show | 39 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.644+487A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794495 | ||||||
chr1:7794603
|
A | G | 1 | a0007c0009t0001g0317 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.644+595A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794603 | ||||||
chr1:7794686
|
G | C | 1 | a0001c0001t0001g0318 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.644+678G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794686 | ||||||
chr1:7794903
|
A | G | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.644+895A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794903 | ||||||
chr1:7794938
|
G | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(146): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.644+930G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7794938 | ||||||
chr1:7795001
|
A | G | 1 | a0002c0016t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.644+993A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795001 | ||||||
chr1:7795101
|
G | A | 4 | a0001c0004t0002g0008a0001c0004t0002g0173a0001c0004t0002g0174others(1): Show | 5 | HG02258.hp2 HG02630.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+1093G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795101 | ||||||
chr1:7795322
|
G | A | 15 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(12): Show | 15 | HG02056.hp1 HG02129.hp2 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.644+1314G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795322 | ||||||
chr1:7795361
|
T | G | 3 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.644+1353T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795361 | ||||||
chr1:7795375
|
A | G | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.644+1367A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795375 | ||||||
chr1:7795375
|
A | T | 2 | a0003c0005t0001g0005a0003c0005t0001g0154 | 3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.644+1367A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795375 | ||||||
chr1:7795423
|
G | A | 1 | a0002c0002t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.644+1415G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795423 | ||||||
chr1:7795434
|
G | A | 83 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0007t0001g0011others(80): Show | 85 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.644+1426G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795434 | ||||||
chr1:7795448
|
G | A | 1 | a0001c0001t0001g0319 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.644+1440G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795448 | ||||||
chr1:7795516
|
C | T | 2 | a0003c0005t0001g0005a0003c0005t0001g0154 | 3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.644+1508C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795516 | ||||||
chr1:7795650
|
A | G | 1 | a0009c0015t0001g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.644+1642A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795650 | ||||||
chr1:7795673
|
G | A | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.644+1665G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795673 | ||||||
chr1:7795682
|
C | T | 14 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(11): Show | 15 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.644+1674C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795682 | ||||||
chr1:7795721
|
G | A | 1 | a0002c0002t0012g0200 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.644+1713G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795721 | ||||||
chr1:7795754
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 247 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.644+1746A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795754 | ||||||
chr1:7795850
|
C | T | 2 | a0009c0015t0001g0054a0009c0015t0001g0055 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.644+1842C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795850 | ||||||
chr1:7795921
|
C | T | 1 | a0001c0003t0001g0147 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.644+1913C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7795921 | ||||||
chr1:7796080
|
C | T | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.644+2072C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796080 | ||||||
chr1:7796206
|
G | C | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.644+2198G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796206 | ||||||
chr1:7796207
|
C | A | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.644+2199C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796207 | ||||||
chr1:7796286
|
T | C | 123 | a0001c0004t0011g0058a0002c0002t0001g0009a0002c0002t0001g0010others(120): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.645-2239T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796286 | ||||||
chr1:7796319
|
C | CT | 130 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(127): Show | 139 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.645-2189dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | |||||
chr1:7796319
|
C | CTTT | 58 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(55): Show | 58 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.645-2191_645-2189d others(5): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | |||||
chr1:7796319
|
C | CTTTTTT | 26 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(23): Show | 28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.645-2194_645-2189d others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | |||||
chr1:7796319
|
C | CTTTTTTT others(1): Show |
84 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.645-2196_645-2189d others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | |||||
chr1:7796319
|
C | CTTTTTTT others(2): Show |
21 | a0002c0002t0001g0190a0002c0002t0001g0201a0002c0002t0001g0244others(18): Show | 21 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.645-2197_645-2189d others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | |||||
chr1:7796319
|
C | CTTTTTTT others(3): Show |
8 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0191others(5): Show | 9 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.645-2198_645-2189d others(12): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | |||||
chr1:7796319
|
C | CTTTTTTT others(4): Show |
2 | a0002c0002t0001g0194a0002c0002t0001g0275 | 2 | HG02572.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.645-2199_645-2189d others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | |||||
chr1:7796319
|
CTT | C | 6 | a0001c0004t0011g0058a0002c0002t0001g0059a0002c0002t0001g0060others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.645-2190_645-2189d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7796319 | |||||
chr1:7796444
|
A | G | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.645-2081A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796444 | ||||||
chr1:7796476
|
A | G | 4 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.645-2049A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796476 | ||||||
chr1:7796514
|
C | T | 2 | a0001c0007t0001g0265a0001c0007t0001g0268 | 2 | NA18944.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.645-2011C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796514 | ||||||
chr1:7796709
|
C | T | 1 | a0004c0006t0001g0025 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.645-1816C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796709 | ||||||
chr1:7796748
|
G | A | 1 | a0002c0012t0001g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.645-1777G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796748 | ||||||
chr1:7796906
|
C | G | 1 | a0013c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.645-1619C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7796906 | ||||||
chr1:7797188
|
GTGTGAGC others(5): Show |
G | 216 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(213): Show | 221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.645-1320_645-1309d others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7797188 | |||||
chr1:7797249
|
G | A | 26 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(23): Show | 31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.645-1276G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797249 | ||||||
chr1:7797314
|
G | C | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(11): Show | 16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.645-1211G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797314 | ||||||
chr1:7797372
|
C | T | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.645-1153C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797372 | ||||||
chr1:7797466
|
C | G | 2 | a0002c0002t0001g0241a0002c0002t0001g0242 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.645-1059C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797466 | ||||||
chr1:7797636
|
T | TA | 55 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(52): Show | 55 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.645-873dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7797636 | |||||
chr1:7797636
|
TA | T | 28 | a0001c0001t0001g0353a0001c0001t0001g0388a0001c0004t0001g0166others(25): Show | 29 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.645-873delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 7797636 | |||||
chr1:7797645
|
A | AG | 5 | a0001c0003t0001g0110a0001c0003t0001g0143a0001c0003t0001g0144others(2): Show | 5 | NA18956.hp2 NA18957.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.645-880_645-879ins others(1): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797645 | ||||||
chr1:7797645
|
A | G | 1 | a0002c0002t0001g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.645-880A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797645 | ||||||
chr1:7797646
|
A | G | 2 | a0001c0001t0001g0305a0001c0001t0001g0355 | 2 | HG00408.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.645-879A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797646 | ||||||
chr1:7797718
|
A | G | 1 | a0004c0006t0001g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.645-807A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797718 | ||||||
chr1:7797848
|
G | A | 1 | a0001c0004t0001g0013 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.645-677G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797848 | ||||||
chr1:7797872
|
C | T | 1 | a0001c0001t0001g0352 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.645-653C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797872 | ||||||
chr1:7797914
|
C | T | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.645-611C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797914 | ||||||
chr1:7797948
|
G | A | 62 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.645-577G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7797948 | ||||||
chr1:7798048
|
A | G | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.645-477A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7798048 | ||||||
chr1:7798075
|
G | C | 31 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0013others(28): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.645-450G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7798075 | ||||||
chr1:7798112
|
G | A | 1 | a0001c0004t0001g0161 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.645-413G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7798112 | ||||||
chr1:7798226
|
G | C | 1 | a0001c0001t0013g0311 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.645-299G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 6/21 | chr1 | 7798226 | ||||||
chr1:7798739
|
G | A | 1 | a0002c0002t0001g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793+66G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7798739 | ||||||
chr1:7798865
|
T | C | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.793+192T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7798865 | ||||||
chr1:7799131
|
A | C | 70 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.793+458A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799131 | ||||||
chr1:7799257
|
G | A | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.793+584G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799257 | ||||||
chr1:7799260
|
C | G | 153 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(150): Show | 158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.793+587C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799260 | ||||||
chr1:7799419
|
G | A | 3 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.793+746G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799419 | ||||||
chr1:7799604
|
C | CT | 153 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(150): Show | 158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.793+932dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7799604 | |||||
chr1:7799610
|
C | CA | 18 | a0001c0001t0001g0368a0001c0003t0001g0097a0001c0003t0001g0116others(15): Show | 21 | HG00639.hp2 HG01109.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.793+957dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7799610 | |||||
chr1:7799610
|
CA | C | 156 | a0001c0001t0001g0020a0001c0001t0001g0296a0001c0001t0001g0301others(153): Show | 162 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.793+957delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7799610 | |||||
chr1:7799925
|
C | T | 1 | a0004c0006t0001g0025 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.794-1188C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7799925 | ||||||
chr1:7799936
|
T | TTTTA | 4 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1161_794-1158d others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7799936 | |||||
chr1:7800047
|
G | A | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.794-1066G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800047 | ||||||
chr1:7800157
|
C | T | 1 | a0001c0017t0001g0165 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.794-956C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800157 | ||||||
chr1:7800216
|
A | AT | 78 | a0001c0003t0004g0108a0002c0002t0001g0009a0002c0002t0001g0188others(75): Show | 82 | HG00621.hp1 HG00642.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.794-886dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7800216 | |||||
chr1:7800216
|
AT | A | 28 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(25): Show | 33 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.794-886delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7800216 | |||||
chr1:7800320
|
G | T | 153 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(150): Show | 158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.794-793G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800320 | ||||||
chr1:7800332
|
C | T | 62 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.794-781C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800332 | ||||||
chr1:7800487
|
C | T | 3 | a0002c0013t0005g0091a0002c0013t0005g0092a0016c0027t0005g0089 | 3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.794-626C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800487 | ||||||
chr1:7800488
|
G | A | 2 | a0001c0003t0001g0093a0001c0003t0001g0152 | 2 | NA18969.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.794-625G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800488 | ||||||
chr1:7800553
|
C | A | 1 | a0001c0001t0001g0015 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.794-560C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800553 | ||||||
chr1:7800691
|
G | A | 1 | a0004c0006t0015g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.794-422G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800691 | ||||||
chr1:7800699
|
C | T | 1 | a0001c0003t0001g0140 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.794-414C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800699 | ||||||
chr1:7800827
|
C | CA | 222 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(219): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.794-271dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7800827 | |||||
chr1:7800841
|
A | AG | 153 | a0001c0004t0011g0058a0002c0002t0001g0009a0002c0002t0001g0010others(150): Show | 158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.794-272_794-271ins others(1): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7800841 | ||||||
chr1:7801008
|
A | G | 3 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.794-105A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7801008 | ||||||
chr1:7801093
|
C | CT | 152 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.794-17dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 7801093 | |||||
chr1:7801098
|
T | G | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.794-15T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 7/21 | chr1 | 7801098 | ||||||
chr1:7801230
|
A | G | 1 | a0005c0025t0014g0266 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.872+39A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801230 | ||||||
chr1:7801244
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(162): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.872+53T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801244 | ||||||
chr1:7801285
|
G | A | 216 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(213): Show | 221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.872+94G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801285 | ||||||
chr1:7801458
|
T | C | 1 | a0001c0004t0001g0306 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.872+267T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801458 | ||||||
chr1:7801540
|
C | A | 123 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 131 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.872+349C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801540 | ||||||
chr1:7801624
|
A | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(125): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.872+433A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801624 | ||||||
chr1:7801772
|
G | A | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.872+581G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801772 | ||||||
chr1:7801832
|
C | A | 1 | a0001c0020t0001g0315 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.872+641C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801832 | ||||||
chr1:7801894
|
A | T | 3 | a0002c0002t0001g0215a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG00408.hp1 HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.872+703A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801894 | ||||||
chr1:7801922
|
G | T | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.872+731G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7801922 | ||||||
chr1:7801980
|
G | GTCAC | 5 | a0002c0002t0001g0235a0002c0002t0001g0236a0002c0002t0001g0269others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+790_872+791ins others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 7801980 | |||||
chr1:7802184
|
C | A | 1 | a0002c0002t0001g0245 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.873-863C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802184 | ||||||
chr1:7802261
|
G | GT | 33 | a0001c0001t0001g0345a0001c0001t0001g0346a0004c0006t0001g0003others(30): Show | 34 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.873-778dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 7802261 | |||||
chr1:7802261
|
G | GTT | 6 | a0002c0002t0001g0059a0002c0002t0001g0060a0002c0002t0001g0061others(3): Show | 6 | HG02257.hp2 HG02717.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.873-779_873-778dup others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 7802261 | |||||
chr1:7802306
|
G | A | 2 | a0004c0006t0001g0025a0004c0006t0001g0036 | 2 | HG00642.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.873-741G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802306 | ||||||
chr1:7802379
|
C | T | 1 | a0001c0003t0001g0139 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.873-668C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802379 | ||||||
chr1:7802512
|
G | A | 123 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(120): Show | 126 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.873-535G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802512 | ||||||
chr1:7802534
|
G | T | 4 | a0001c0003t0001g0113a0001c0003t0001g0137a0001c0003t0001g0138others(1): Show | 4 | NA18948.hp1 NA18954.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-513G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802534 | ||||||
chr1:7802567
|
G | A | 1 | a0011c0018t0017g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.873-480G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802567 | ||||||
chr1:7802632
|
ACATCAT | A | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.873-412_873-407del others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 7802632 | |||||
chr1:7802764
|
A | G | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.873-283A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802764 | ||||||
chr1:7802839
|
T | C | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.873-208T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802839 | ||||||
chr1:7802991
|
A | T | 9 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(6): Show | 10 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-56A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802991 | ||||||
chr1:7802996
|
A | G | 1 | a0002c0002t0001g0186 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.873-51A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 8/21 | chr1 | 7802996 | ||||||
chr1:7803228
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0296 | 2 | NA18965.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.979+75T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803228 | ||||||
chr1:7803233
|
C | T | 152 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.979+80C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803233 | ||||||
chr1:7803271
|
T | C | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.979+118T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803271 | ||||||
chr1:7803359
|
T | C | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+206T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803359 | ||||||
chr1:7803365
|
A | G | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+212A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803365 | ||||||
chr1:7803367
|
TTG | T | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+215_979+216del others(2): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803367 | ||||||
chr1:7803371
|
C | A | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+218C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803371 | ||||||
chr1:7803372
|
T | C | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+219T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803372 | ||||||
chr1:7803384
|
T | A | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+231T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803384 | ||||||
chr1:7803386
|
G | C | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+233G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803386 | ||||||
chr1:7803394
|
G | T | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+241G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803394 | ||||||
chr1:7803397
|
T | C | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+244T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803397 | ||||||
chr1:7803401
|
C | T | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+248C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803401 | ||||||
chr1:7803404
|
C | A | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+251C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803404 | ||||||
chr1:7803406
|
T | C | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+253T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803406 | ||||||
chr1:7803410
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.979+257G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803410 | ||||||
chr1:7803411
|
T | A | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+258T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803411 | ||||||
chr1:7803413
|
A | AC | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+263dupC | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803413 | |||||
chr1:7803417
|
A | G | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+264A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803417 | ||||||
chr1:7803421
|
A | C | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.979+268A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803421 | ||||||
chr1:7803430
|
G | A | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.980-262G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803430 | ||||||
chr1:7803433
|
C | CAAAAAAT others(162): Show |
2 | a0009c0015t0001g0054a0009c0015t0001g0055 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.980-254_980-253ins others(169): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | |||||
chr1:7803433
|
C | CAAAAAAT others(165): Show |
1 | a0002c0002t0001g0193 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.980-254_980-253ins others(172): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | |||||
chr1:7803433
|
C | CAAAAAAT others(168): Show |
1 | a0002c0002t0012g0200 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.980-254_980-253ins others(175): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | |||||
chr1:7803433
|
C | CAAAAAAT others(177): Show |
2 | a0002c0002t0001g0009a0002c0002t0001g0190 | 3 | HG01168.hp1 HG01255.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.980-254_980-253ins others(184): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | |||||
chr1:7803433
|
C | CAAAAAAT others(178): Show |
4 | a0002c0002t0001g0188a0002c0002t0001g0192a0002c0002t0001g0194others(1): Show | 4 | HG00733.hp1 HG02572.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.980-254_980-253ins others(185): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | |||||
chr1:7803433
|
C | CAAAAAAT others(179): Show |
2 | a0002c0002t0001g0191a0002c0002t0001g0274 | 2 | HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.980-254_980-253ins others(186): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | |||||
chr1:7803433
|
C | CAAAAAAT others(181): Show |
3 | a0002c0002t0001g0197a0002c0002t0001g0198a0002c0002t0001g0199 | 3 | HG02145.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.980-254_980-253ins others(188): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | |||||
chr1:7803433
|
C | CAAAAAAT others(190): Show |
1 | a0002c0002t0001g0196 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.980-254_980-253ins others(197): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | |||||
chr1:7803433
|
C | CAAAAAAT others(194): Show |
1 | a0002c0002t0001g0195 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.980-254_980-253ins others(201): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803433 | |||||
chr1:7803570
|
A | G | 1 | a0007c0009t0001g0344 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.980-122A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | chr1 | 7803570 | ||||||
chr1:7803675
|
CTTA | C | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.980-11_980-9delATT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 7803675 | |||||
chr1:7803880
|
C | T | 1 | a0002c0002t0012g0200 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1136+32C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7803880 | ||||||
chr1:7803884
|
T | G | 8 | a0001c0004t0001g0013a0001c0004t0001g0306a0001c0004t0001g0307others(5): Show | 9 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1136+36T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7803884 | ||||||
chr1:7803970
|
G | A | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1136+122G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7803970 | ||||||
chr1:7804051
|
A | G | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1136+203A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804051 | ||||||
chr1:7804145
|
T | A | 1 | a0001c0001t0001g0347 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1136+297T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804145 | ||||||
chr1:7804223
|
A | G | 1 | a0004c0006t0001g0030 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1136+375A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804223 | ||||||
chr1:7804311
|
C | CT | 38 | a0001c0001t0001g0288a0001c0003t0001g0106a0001c0003t0001g0107others(35): Show | 41 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.1136+478dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804311 | |||||
chr1:7804311
|
CT | C | 16 | a0001c0001t0001g0321a0001c0001t0001g0356a0001c0001t0001g0369others(13): Show | 16 | HG00280.hp1 HG01975.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.1136+478delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804311 | |||||
chr1:7804398
|
C | CT | 33 | a0001c0003t0001g0116a0001c0007t0001g0011a0001c0007t0001g0255others(30): Show | 36 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1136+565dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804398 | |||||
chr1:7804497
|
C | T | 1 | a0001c0003t0001g0136 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1136+649C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804497 | ||||||
chr1:7804608
|
CCAGGCTG others(4): Show |
C | 1 | a0001c0004t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1136+763_1136+773d others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804608 | |||||
chr1:7804694
|
G | A | 1 | a0004c0006t0001g0035 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1136+846G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804694 | ||||||
chr1:7804813
|
C | T | 1 | a0003c0005t0001g0073 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1136+965C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804813 | ||||||
chr1:7804873
|
C | CT | 202 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(199): Show | 206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1136+1038dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804873 | |||||
chr1:7804873
|
C | CTT | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1136+1037_1136+103 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7804873 | |||||
chr1:7804976
|
C | A | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1136+1128C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7804976 | ||||||
chr1:7805003
|
G | A | 92 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(89): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1136+1155G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805003 | ||||||
chr1:7805018
|
G | A | 4 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187others(1): Show | 4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136+1170G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805018 | ||||||
chr1:7805224
|
C | T | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1136+1376C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805224 | ||||||
chr1:7805286
|
GA | G | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG03041.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1136+1440delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7805286 | |||||
chr1:7805407
|
C | T | 92 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(89): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1136+1559C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805407 | ||||||
chr1:7805485
|
G | A | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1136+1637G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805485 | ||||||
chr1:7805573
|
A | G | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1136+1725A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805573 | ||||||
chr1:7805618
|
G | C | 2 | a0002c0002t0001g0009a0002c0002t0001g0188 | 3 | HG00733.hp1 HG01168.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1136+1770G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805618 | ||||||
chr1:7805631
|
A | T | 92 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(89): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1136+1783A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805631 | ||||||
chr1:7805634
|
C | T | 1 | a0002c0002t0001g0238 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1136+1786C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805634 | ||||||
chr1:7805650
|
C | T | 27 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(24): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1136+1802C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805650 | ||||||
chr1:7805927
|
A | G | 1 | a0001c0001t0001g0376 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1136+2079A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805927 | ||||||
chr1:7805977
|
T | C | 1 | a0003c0005t0001g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1136+2129T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7805977 | ||||||
chr1:7806023
|
G | A | 123 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(120): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1136+2175G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806023 | ||||||
chr1:7806080
|
C | T | 2 | a0009c0015t0001g0054a0009c0015t0001g0055 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1136+2232C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806080 | ||||||
chr1:7806196
|
T | C | 1 | a0003c0005t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1136+2348T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806196 | ||||||
chr1:7806222
|
C | T | 2 | a0003c0005t0001g0005a0003c0005t0001g0154 | 3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1136+2374C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806222 | ||||||
chr1:7806350
|
G | A | 29 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(26): Show | 31 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.1136+2502G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806350 | ||||||
chr1:7806405
|
A | C | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1137-2488A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806405 | ||||||
chr1:7806554
|
G | A | 29 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(26): Show | 31 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.1137-2339G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806554 | ||||||
chr1:7806646
|
T | C | 1 | a0002c0021t0001g0379 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1137-2247T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806646 | ||||||
chr1:7806756
|
T | A | 1 | a0002c0002t0001g0245 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1137-2137T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806756 | ||||||
chr1:7806777
|
G | C | 1 | a0004c0006t0001g0050 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1137-2116G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806777 | ||||||
chr1:7806795
|
T | TA | 9 | a0001c0004t0002g0008a0001c0004t0002g0169a0001c0004t0002g0170others(6): Show | 11 | HG00140.hp2 HG01074.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1137-2080dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806795 | |||||
chr1:7806795
|
T | TAAAAAAA others(4): Show |
1 | a0001c0003t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1137-2090_1137-208 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806795 | |||||
chr1:7806795
|
TAAA | T | 26 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0063others(23): Show | 28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1137-2082_1137-208 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806795 | |||||
chr1:7806801
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1137-2092A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806801 | ||||||
chr1:7806802
|
A | ATATATAT others(8): Show |
1 | a0001c0007t0001g0268 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1137-2091_1137-209 others(19): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806802 | ||||||
chr1:7806804
|
A | T | 2 | a0001c0007t0001g0268a0002c0021t0001g0379 | 2 | NA18944.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1137-2089A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806804 | ||||||
chr1:7806806
|
A | AATATATA others(1): Show |
6 | a0001c0001t0001g0366a0002c0002t0001g0022a0002c0002t0001g0023others(3): Show | 6 | NA18953.hp2 NA18972.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1137-2086_1137-208 others(12): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | |||||
chr1:7806806
|
A | AATATATA others(5): Show |
5 | a0001c0001t0001g0263a0001c0007t0001g0365a0002c0002t0001g0229others(2): Show | 5 | HG00544.hp2 NA18995.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-2086_1137-208 others(16): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | |||||
chr1:7806806
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0372 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1137-2086_1137-208 others(18): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | |||||
chr1:7806806
|
A | AATATATA others(9): Show |
1 | a0002c0002t0001g0228 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1137-2086_1137-208 others(20): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | |||||
chr1:7806806
|
A | AATATATA others(15): Show |
2 | a0001c0001t0001g0364a0001c0007t0001g0262 | 2 | HG02056.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1137-2086_1137-208 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806806 | |||||
chr1:7806806
|
A | ATAT | 3 | a0002c0002t0001g0186a0002c0002t0001g0236a0002c0002t0001g0277 | 3 | HG02258.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1137-2087_1137-208 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806806 | ||||||
chr1:7806806
|
A | T | 8 | a0001c0001t0001g0284a0001c0001t0001g0383a0001c0007t0001g0268others(5): Show | 8 | HG00673.hp2 HG02129.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-2087A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806806 | ||||||
chr1:7806807
|
AAAAAAAT others(6): Show |
A | 1 | a0002c0002t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1137-2084_1137-207 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806807 | |||||
chr1:7806808
|
A | AATAT | 17 | a0001c0001t0001g0019a0001c0001t0001g0283a0001c0001t0001g0298others(14): Show | 18 | HG00733.hp2 HG01070.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | |||||
chr1:7806808
|
A | AATATAT | 10 | a0001c0001t0001g0015a0001c0001t0001g0180a0001c0001t0001g0333others(7): Show | 11 | HG00741.hp2 HG01069.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | |||||
chr1:7806808
|
A | AATATATA others(3): Show |
6 | a0001c0001t0001g0287a0001c0001t0001g0354a0002c0002t0001g0053others(3): Show | 6 | HG01109.hp2 HG01433.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | |||||
chr1:7806808
|
A | AATATATA others(5): Show |
2 | a0001c0001t0001g0296a0001c0001t0001g0367 | 2 | HG04184.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(16): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | |||||
chr1:7806808
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0346a0001c0001t0001g0361 | 2 | HG04115.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1137-2084_1137-208 others(18): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | |||||
chr1:7806808
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0360 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1137-2084_1137-208 others(20): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | |||||
chr1:7806808
|
A | AATATATA others(11): Show |
1 | a0002c0013t0001g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1137-2084_1137-208 others(22): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806808 | |||||
chr1:7806808
|
A | ATATAT | 18 | a0001c0001t0001g0318a0001c0001t0001g0340a0001c0001t0001g0376others(15): Show | 18 | HG00408.hp1 HG00621.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-2085_1137-208 others(9): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | ||||||
chr1:7806808
|
A | ATATATAT | 7 | a0001c0001t0001g0339a0001c0007t0001g0261a0002c0002t0001g0183others(4): Show | 7 | HG02027.hp2 HG02717.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137-2085_1137-208 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | ||||||
chr1:7806808
|
A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0314a0002c0002t0001g0226a0002c0002t0001g0267 | 3 | HG02738.hp2 NA18965.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1137-2085_1137-208 others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | ||||||
chr1:7806808
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0363 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1137-2085_1137-208 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | ||||||
chr1:7806808
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0294a0001c0001t0001g0362 | 2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1137-2085_1137-208 others(19): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | ||||||
chr1:7806808
|
A | T | 34 | a0001c0001t0001g0263a0001c0001t0001g0284a0001c0001t0001g0295others(31): Show | 34 | HG00280.hp2 HG00544.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1137-2085A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806808 | ||||||
chr1:7806810
|
A | AATAT | 24 | a0001c0001t0001g0291a0001c0001t0001g0297a0001c0001t0001g0321others(21): Show | 25 | HG00642.hp1 HG01069.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1137-2082_1137-208 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | |||||
chr1:7806810
|
A | AATATAT | 5 | a0001c0001t0001g0016a0001c0001t0001g0348a0001c0004t0001g0166others(2): Show | 6 | HG00099.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-2082_1137-208 others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | |||||
chr1:7806810
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0341 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | |||||
chr1:7806810
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0290 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(18): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | |||||
chr1:7806810
|
A | AATATATA others(11): Show |
1 | a0001c0001t0001g0302 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(22): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | |||||
chr1:7806810
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0303 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | |||||
chr1:7806810
|
A | AATATATA others(17): Show |
1 | a0001c0001t0001g0289 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1137-2082_1137-208 others(28): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806810 | |||||
chr1:7806810
|
A | ATAT | 12 | a0001c0001t0001g0288a0001c0001t0001g0319a0001c0001t0001g0329others(9): Show | 12 | HG00140.hp1 HG00423.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.1137-2083_1137-208 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806810
|
A | ATATAT | 29 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0020others(26): Show | 32 | HG00558.hp1 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1137-2083_1137-208 others(9): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806810
|
A | ATATATAT | 11 | a0001c0001t0001g0264a0001c0001t0001g0352a0001c0001t0001g0355others(8): Show | 12 | HG00408.hp2 HG00735.hp2 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.1137-2083_1137-208 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806810
|
A | ATATATAT others(2): Show |
9 | a0001c0001t0001g0293a0001c0001t0001g0305a0001c0001t0001g0343others(6): Show | 9 | HG00438.hp2 HG01257.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137-2083_1137-208 others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806810
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806810
|
A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0202 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806810
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0286 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(25): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806810
|
A | ATATATAT others(16): Show |
1 | a0002c0012t0001g0177 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806810
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0292 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1137-2083_1137-208 others(33): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806810
|
A | T | 124 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0180others(121): Show | 127 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1137-2083A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806810 | ||||||
chr1:7806811
|
AAAT | A | 11 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(8): Show | 12 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806811 | |||||
chr1:7806812
|
A | AAAAAAAA others(10): Show |
1 | a0001c0003t0001g0143 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(21): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(16): Show |
1 | a0001c0003t0001g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(22): Show |
1 | a0001c0003t0001g0116 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(33): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(15): Show |
2 | a0001c0003t0001g0117a0001c0003t0001g0139 | 2 | HG02027.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(17): Show |
1 | a0006c0010t0001g0096 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(28): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(19): Show |
2 | a0001c0003t0001g0141a0001c0003t0001g0150 | 2 | NA18946.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(30): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(12): Show |
1 | a0001c0003t0001g0146 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(23): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(14): Show |
6 | a0001c0003t0001g0095a0001c0003t0001g0109a0001c0003t0001g0110others(3): Show | 6 | HG01981.hp2 HG02135.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(25): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(16): Show |
4 | a0001c0003t0001g0114a0001c0003t0001g0120a0001c0003t0001g0144others(1): Show | 4 | HG01074.hp2 HG02071.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(18): Show |
3 | a0001c0003t0001g0113a0001c0003t0001g0137a0001c0003t0001g0138 | 3 | NA18954.hp2 NA18978.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(29): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(22): Show |
1 | a0001c0003t0001g0140 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(33): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(13): Show |
4 | a0001c0003t0001g0106a0001c0003t0001g0126a0006c0010t0001g0124others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(24): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(15): Show |
3 | a0001c0003t0001g0111a0001c0003t0001g0123a0001c0003t0001g0147 | 3 | NA18986.hp2 NA18987.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(17): Show |
2 | a0001c0003t0001g0101a0001c0028t0001g0122 | 2 | HG00544.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(28): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0118 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(30): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(12): Show |
2 | a0001c0003t0001g0107a0006c0010t0001g0133 | 2 | HG00741.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(23): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(14): Show |
10 | a0001c0003t0001g0062a0001c0003t0001g0097a0001c0003t0001g0129others(7): Show | 10 | HG00621.hp1 HG01099.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(25): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(18): Show |
1 | a0001c0003t0001g0148 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(29): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(20): Show |
1 | a0001c0003t0001g0128 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(31): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(26): Show |
1 | a0001c0003t0001g0127 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(37): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(11): Show |
1 | a0001c0003t0001g0151 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(22): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(13): Show |
1 | a0001c0003t0001g0098 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(24): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(15): Show |
3 | a0001c0003t0001g0103a0001c0003t0001g0112a0001c0003t0001g0152 | 3 | HG00438.hp1 HG00673.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(12): Show |
2 | a0001c0003t0001g0104a0001c0003t0001g0142 | 2 | HG01496.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(23): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(18): Show |
1 | a0001c0003t0001g0134 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(29): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(13): Show |
1 | a0001c0003t0001g0105 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(24): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(15): Show |
1 | a0001c0003t0001g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(19): Show |
1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(30): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAAAAA others(16): Show |
1 | a0001c0003t0001g0153 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAAATAT others(4): Show |
1 | a0016c0027t0005g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAATATA others(3): Show |
2 | a0002c0013t0005g0091a0002c0013t0005g0092 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AAAATATA others(7): Show |
2 | a0001c0001t0001g0359a0002c0012t0001g0179 | 2 | HG02055.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1137-2080_1137-207 others(18): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AATAT | 9 | a0001c0001t0001g0368a0001c0001t0001g0369a0001c0004t0001g0006others(6): Show | 11 | HG01261.hp2 HG02155.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137-2060_1137-205 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AATATATA others(3): Show |
1 | a0001c0007t0001g0256 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1137-2066_1137-205 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0301 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1137-2078_1137-205 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806812 | |||||
chr1:7806812
|
A | ATAT | 3 | a0001c0001t0001g0002a0001c0001t0001g0373a0001c0004t0002g0171 | 5 | HG02809.hp1 HG03130.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-2081_1137-208 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | ||||||
chr1:7806812
|
A | ATATAT | 15 | a0001c0001t0001g0312a0001c0004t0001g0163a0001c0004t0001g0307others(12): Show | 15 | HG00280.hp1 HG01106.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137-2081_1137-208 others(9): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | ||||||
chr1:7806812
|
A | ATATATAT | 7 | a0001c0001t0001g0345a0001c0001t0013g0311a0001c0007t0001g0203others(4): Show | 7 | HG00639.hp1 HG02155.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137-2081_1137-208 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | ||||||
chr1:7806812
|
A | ATATATAT others(2): Show |
3 | a0002c0002t0001g0205a0002c0002t0001g0206a0002c0002t0001g0246 | 3 | HG01261.hp1 HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1137-2081_1137-208 others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | ||||||
chr1:7806812
|
A | ATATATAT others(4): Show |
1 | a0002c0002t0001g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1137-2081_1137-208 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | ||||||
chr1:7806812
|
A | ATATATAT others(6): Show |
1 | a0007c0009t0001g0317 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1137-2081_1137-208 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | ||||||
chr1:7806812
|
A | T | 236 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(233): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1137-2081A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806812 | ||||||
chr1:7806813
|
A | AAAAAAAA others(20): Show |
1 | a0001c0003t0001g0136 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1137-2080_1137-207 others(31): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806813 | ||||||
chr1:7806814
|
T | A | 4 | a0001c0003t0001g0135a0001c0004t0002g0168a0009c0015t0001g0054others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-2079T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806814 | ||||||
chr1:7806816
|
T | A | 1 | a0001c0003t0001g0135 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137-2077T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806816 | ||||||
chr1:7806818
|
T | A | 1 | a0001c0003t0001g0135 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137-2075T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806818 | ||||||
chr1:7806820
|
T | A | 1 | a0001c0003t0001g0135 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137-2073T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806820 | ||||||
chr1:7806836
|
T | TA | 60 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0095others(57): Show | 60 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1137-2057_1137-205 others(5): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806836 | ||||||
chr1:7806837
|
T | A | 2 | a0001c0003t0001g0094a0001c0003t0001g0136 | 2 | HG02040.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1137-2056T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806837 | ||||||
chr1:7806838
|
A | T | 2 | a0001c0003t0001g0094a0001c0003t0001g0136 | 2 | HG02040.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1137-2055A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806838 | ||||||
chr1:7806839
|
C | A | 2 | a0001c0003t0001g0094a0001c0003t0001g0136 | 2 | HG02040.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1137-2054C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806839 | ||||||
chr1:7806839
|
C | T | 60 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0095others(57): Show | 60 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1137-2054C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806839 | ||||||
chr1:7806840
|
A | AT | 60 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0095others(57): Show | 60 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1137-2052dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806840 | |||||
chr1:7806840
|
A | G | 3 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1137-2053A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806840 | ||||||
chr1:7806840
|
A | T | 2 | a0001c0003t0001g0094a0001c0003t0001g0136 | 2 | HG02040.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1137-2053A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806840 | ||||||
chr1:7806841
|
T | TAC | 5 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(2): Show | 5 | HG00735.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-2040_1137-203 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7806841 | |||||
chr1:7806855
|
T | C | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1137-2038T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7806855 | ||||||
chr1:7807084
|
C | T | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-1809C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807084 | ||||||
chr1:7807195
|
G | A | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1137-1698G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807195 | ||||||
chr1:7807256
|
T | C | 1 | a0002c0012t0001g0177 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1137-1637T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807256 | ||||||
chr1:7807285
|
T | C | 1 | a0002c0002t0001g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1137-1608T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807285 | ||||||
chr1:7807325
|
G | A | 2 | a0001c0004t0002g0008a0001c0004t0002g0173 | 3 | HG02258.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1137-1568G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807325 | ||||||
chr1:7807394
|
T | C | 3 | a0002c0013t0005g0091a0002c0013t0005g0092a0016c0027t0005g0089 | 3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1137-1499T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807394 | ||||||
chr1:7807686
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1137-1207G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7807686 | ||||||
chr1:7808061
|
C | T | 4 | a0004c0006t0001g0026a0004c0006t0001g0029a0004c0006t0001g0030others(1): Show | 4 | HG01109.hp2 HG01433.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137-832C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808061 | ||||||
chr1:7808116
|
C | A | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-777C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808116 | ||||||
chr1:7808160
|
G | A | 1 | a0013c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1137-733G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808160 | ||||||
chr1:7808232
|
C | CA | 74 | a0001c0003t0001g0148a0001c0004t0011g0058a0002c0002t0001g0009others(71): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1137-634dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | |||||
chr1:7808232
|
C | CAA | 63 | a0001c0003t0001g0062a0001c0003t0001g0094a0001c0003t0001g0095others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1137-635_1137-634d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | |||||
chr1:7808232
|
C | CAAA | 22 | a0001c0003t0001g0093a0001c0003t0001g0098a0001c0003t0001g0101others(19): Show | 22 | HG00735.hp1 HG01192.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1137-636_1137-634d others(5): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | |||||
chr1:7808232
|
C | CAAAA | 12 | a0001c0003t0001g0110a0001c0003t0001g0146a0003c0005t0001g0004others(9): Show | 13 | HG00738.hp1 HG01123.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1137-637_1137-634d others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | |||||
chr1:7808232
|
C | CAAAAA | 12 | a0003c0005t0001g0064a0003c0005t0001g0065a0003c0005t0001g0066others(9): Show | 12 | HG01106.hp2 HG01175.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1137-638_1137-634d others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | |||||
chr1:7808232
|
C | CAAAAAA | 5 | a0003c0005t0001g0005a0003c0005t0001g0063a0003c0005t0001g0080others(2): Show | 6 | HG02895.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-639_1137-634d others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | |||||
chr1:7808232
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0295a0001c0001t0001g0303a0001c0001t0001g0358 | 3 | NA18979.hp1 NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1137-644_1137-634d others(13): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | |||||
chr1:7808232
|
CAAAAAAA others(5): Show |
C | 157 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(154): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1137-645_1137-634d others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 7808232 | |||||
chr1:7808268
|
G | C | 4 | a0001c0001t0001g0333a0001c0001t0001g0335a0001c0001t0001g0346others(1): Show | 4 | HG00733.hp2 HG02293.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-625G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808268 | ||||||
chr1:7808290
|
G | A | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1137-603G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808290 | ||||||
chr1:7808308
|
G | C | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1137-585G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808308 | ||||||
chr1:7808357
|
T | C | 62 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1137-536T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808357 | ||||||
chr1:7808376
|
G | T | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-517G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808376 | ||||||
chr1:7808665
|
T | C | 131 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(128): Show | 134 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.1137-228T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808665 | ||||||
chr1:7808844
|
C | T | 1 | a0002c0012t0001g0177 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1137-49C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 10/21 | chr1 | 7808844 | ||||||
chr1:7809320
|
A | G | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1242+322A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809320 | ||||||
chr1:7809321
|
G | A | 3 | a0001c0003t0001g0117a0001c0003t0001g0121a0001c0003t0001g0139 | 3 | HG02027.hp1 NA18968.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1242+323G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809321 | ||||||
chr1:7809425
|
T | G | 1 | a0002c0002t0001g0195 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1242+427T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809425 | ||||||
chr1:7809437
|
G | A | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1242+439G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809437 | ||||||
chr1:7809533
|
C | T | 1 | a0002c0002t0001g0267 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1243-360C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809533 | ||||||
chr1:7809673
|
C | T | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1243-220C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809673 | ||||||
chr1:7809687
|
A | T | 28 | a0001c0003t0001g0095a0001c0003t0001g0097a0001c0003t0001g0098others(25): Show | 28 | HG00438.hp1 HG00621.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1243-206A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809687 | ||||||
chr1:7809729
|
G | C | 3 | a0001c0001t0001g0381a0001c0011t0001g0018a0001c0011t0001g0351 | 4 | NA19011.hp1 NA19074.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243-164G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809729 | ||||||
chr1:7809855
|
G | C | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1243-38G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 11/21 | chr1 | 7809855 | ||||||
chr1:7810084
|
A | C | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1371+63A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/21 | chr1 | 7810084 | ||||||
chr1:7810141
|
A | G | 1 | a0003c0005t0001g0067 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1371+120A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/21 | chr1 | 7810141 | ||||||
chr1:7810276
|
C | A | 4 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372-162C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/21 | chr1 | 7810276 | ||||||
chr1:7810358
|
C | T | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1372-80C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 12/21 | chr1 | 7810358 | ||||||
chr1:7810655
|
A | C | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1522+67A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7810655 | ||||||
chr1:7811144
|
T | C | 4 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522+556T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811144 | ||||||
chr1:7811169
|
T | C | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1522+581T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811169 | ||||||
chr1:7811190
|
C | T | 4 | a0001c0001t0001g0319a0001c0001t0001g0331a0001c0001t0009g0332others(1): Show | 4 | HG00423.hp1 NA18961.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1522+602C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811190 | ||||||
chr1:7811289
|
A | G | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1522+701A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811289 | ||||||
chr1:7811327
|
A | G | 1 | a0001c0001t0001g0002 | 3 | HG02809.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1522+739A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811327 | ||||||
chr1:7811370
|
A | G | 1 | a0002c0002t0001g0276 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1522+782A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811370 | ||||||
chr1:7811421
|
AG | A | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1522+834delG | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811421 | ||||||
chr1:7811524
|
C | T | 26 | a0001c0003t0001g0095a0001c0003t0001g0097a0001c0003t0001g0098others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.1522+936C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811524 | ||||||
chr1:7811748
|
A | G | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1522+1160A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811748 | ||||||
chr1:7811789
|
C | T | 9 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(6): Show | 10 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1522+1201C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7811789 | ||||||
chr1:7812016
|
A | G | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1522+1428A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812016 | ||||||
chr1:7812128
|
C | T | 1 | a0001c0001t0001g0374 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1522+1540C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812128 | ||||||
chr1:7812267
|
A | AT | 159 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(156): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1522+1688dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812267 | |||||
chr1:7812393
|
G | A | 73 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0289others(70): Show | 76 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1522+1805G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812393 | ||||||
chr1:7812422
|
C | G | 26 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(23): Show | 31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.1522+1834C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812422 | ||||||
chr1:7812423
|
G | A | 1 | a0013c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1522+1835G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812423 | ||||||
chr1:7812493
|
T | C | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1522+1905T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812493 | ||||||
chr1:7812500
|
C | T | 1 | a0002c0012t0001g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1522+1912C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812500 | ||||||
chr1:7812540
|
G | A | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(11): Show | 16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1522+1952G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812540 | ||||||
chr1:7812550
|
G | A | 2 | a0002c0002t0001g0271a0002c0002t0001g0272 | 2 | NA18957.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1522+1962G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812550 | ||||||
chr1:7812582
|
G | A | 10 | a0001c0001t0001g0263a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02056.hp1 HG03834.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.1522+1994G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812582 | ||||||
chr1:7812608
|
G | C | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1522+2020G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812608 | ||||||
chr1:7812624
|
C | CA | 9 | a0001c0001t0001g0331a0001c0001t0001g0352a0001c0001t0001g0364others(6): Show | 9 | HG02056.hp1 HG04184.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.1522+2061dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
C | CAAA | 53 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0095others(50): Show | 54 | HG00544.hp1 HG00621.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1522+2059_1522+206 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
C | CAAAA | 10 | a0001c0003t0001g0097a0001c0003t0001g0103a0001c0003t0001g0110others(7): Show | 10 | HG00438.hp1 HG01975.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1522+2058_1522+206 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
C | CAAAAA | 50 | a0001c0003t0001g0139a0001c0004t0011g0058a0002c0002t0001g0196others(47): Show | 52 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1522+2057_1522+206 others(9): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
C | CAAAAAA | 18 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0191others(15): Show | 19 | HG00733.hp1 HG00735.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1522+2056_1522+206 others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
C | CAAAAAAA | 9 | a0002c0002t0001g0190a0002c0002t0001g0193a0002c0002t0001g0194others(6): Show | 9 | HG01243.hp1 HG01358.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1522+2055_1522+206 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
C | CAAAAAAA others(3): Show |
7 | a0002c0002t0001g0061a0002c0002t0001g0183a0002c0002t0001g0186others(4): Show | 7 | HG02258.hp1 HG02451.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1522+2052_1522+206 others(14): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
C | CAAAAAAA others(4): Show |
7 | a0002c0002t0001g0059a0002c0002t0001g0060a0002c0002t0001g0184others(4): Show | 7 | HG02280.hp1 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1522+2051_1522+206 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
CA | C | 30 | a0001c0001t0001g0288a0001c0001t0001g0297a0001c0001t0001g0301others(27): Show | 35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.1522+2061delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
CAA | C | 7 | a0001c0004t0001g0157a0002c0012t0001g0177a0002c0012t0001g0178others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1522+2060_1522+206 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812624
|
CAAAAAA | C | 52 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(49): Show | 53 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1522+2056_1522+206 others(10): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7812624 | |||||
chr1:7812742
|
T | C | 1 | a0001c0004t0001g0161 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1522+2154T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812742 | ||||||
chr1:7812764
|
T | C | 1 | a0005c0008t0003g0282 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1522+2176T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812764 | ||||||
chr1:7812775
|
G | T | 1 | a0003c0005t0010g0070 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1522+2187G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812775 | ||||||
chr1:7812796
|
A | T | 1 | a0009c0015t0001g0054 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1522+2208A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812796 | ||||||
chr1:7812823
|
G | A | 1 | a0005c0025t0014g0266 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1522+2235G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812823 | ||||||
chr1:7812887
|
T | G | 1 | a0004c0006t0001g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1522+2299T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7812887 | ||||||
chr1:7813015
|
T | C | 27 | a0003c0005t0001g0004a0003c0005t0001g0063a0003c0005t0001g0064others(24): Show | 28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1522+2427T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813015 | ||||||
chr1:7813443
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1522+2855A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813443 | ||||||
chr1:7813491
|
C | T | 1 | a0002c0013t0001g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1522+2903C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813491 | ||||||
chr1:7813533
|
G | A | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1522+2945G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813533 | ||||||
chr1:7813741
|
G | A | 3 | a0002c0002t0001g0210a0002c0002t0001g0232a0002c0002t0001g0234 | 3 | HG00280.hp2 HG01099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1522+3153G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813741 | ||||||
chr1:7813795
|
T | A | 67 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(64): Show | 67 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1522+3207T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813795 | ||||||
chr1:7813979
|
C | A | 4 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522+3391C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813979 | ||||||
chr1:7813982
|
C | G | 4 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522+3394C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813982 | ||||||
chr1:7813983
|
G | A | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1522+3395G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7813983 | ||||||
chr1:7814002
|
A | G | 1 | a0001c0003t0001g0128 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1522+3414A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7814002 | ||||||
chr1:7814186
|
G | A | 22 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0309others(19): Show | 23 | HG00423.hp1 HG00558.hp1 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.1522+3598G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7814186 | ||||||
chr1:7814731
|
C | A | 6 | a0004c0006t0001g0026a0004c0006t0001g0027a0004c0006t0001g0028others(3): Show | 6 | HG01109.hp2 HG01433.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1522+4143C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7814731 | ||||||
chr1:7814915
|
C | T | 32 | a0002c0002t0001g0249a0004c0006t0001g0003a0004c0006t0001g0024others(29): Show | 33 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1522+4327C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7814915 | ||||||
chr1:7815015
|
A | G | 1 | a0002c0002t0001g0202 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1523-4270A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815015 | ||||||
chr1:7815182
|
T | C | 1 | a0002c0002t0001g0226 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1523-4103T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815182 | ||||||
chr1:7815411
|
C | T | 2 | a0003c0005t0001g0005a0003c0005t0001g0154 | 3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1523-3874C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815411 | ||||||
chr1:7815550
|
A | G | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1523-3735A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815550 | ||||||
chr1:7815723
|
C | T | 1 | a0002c0002t0001g0239 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1523-3562C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815723 | ||||||
chr1:7815752
|
G | A | 113 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(110): Show | 118 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1523-3533G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815752 | ||||||
chr1:7815829
|
C | CA | 16 | a0001c0001t0001g0333a0001c0001t0001g0335a0001c0001t0001g0354others(13): Show | 18 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1523-3442dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815829 | |||||
chr1:7815829
|
CA | C | 14 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(11): Show | 15 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1523-3442delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815829 | |||||
chr1:7815986
|
C | T | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1523-3299C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815986 | ||||||
chr1:7815987
|
G | A | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG03041.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1523-3298G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7815987 | ||||||
chr1:7815991
|
C | CA | 97 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(94): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1523-3268dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAA | 73 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(70): Show | 79 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1523-3269_1523-326 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAA | 18 | a0001c0001t0001g0020a0001c0001t0001g0313a0001c0001t0001g0326others(15): Show | 19 | HG01106.hp2 HG01123.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1523-3270_1523-326 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(4): Show |
1 | a0001c0003t0001g0145 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1523-3278_1523-326 others(15): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(5): Show |
4 | a0001c0003t0001g0110a0001c0003t0001g0143a0001c0003t0001g0144others(1): Show | 4 | NA18956.hp2 NA18957.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523-3279_1523-326 others(16): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(8): Show |
1 | a0001c0003t0001g0105 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1523-3282_1523-326 others(19): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(14): Show |
1 | a0006c0010t0001g0125 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1523-3288_1523-326 others(25): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(15): Show |
12 | a0001c0003t0001g0119a0001c0003t0001g0120a0001c0003t0001g0121others(9): Show | 12 | HG01074.hp2 HG01167.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1523-3289_1523-326 others(26): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(16): Show |
16 | a0001c0003t0001g0095a0001c0003t0001g0098a0001c0003t0001g0101others(13): Show | 16 | HG00438.hp1 HG00673.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1523-3290_1523-326 others(27): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(17): Show |
6 | a0001c0003t0001g0104a0001c0003t0001g0113a0001c0003t0001g0135others(3): Show | 6 | HG00621.hp1 HG02004.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1523-3291_1523-326 others(28): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(19): Show |
1 | a0001c0003t0001g0142 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1523-3293_1523-326 others(30): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(20): Show |
1 | a0001c0003t0001g0147 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(31): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(21): Show |
2 | a0001c0003t0001g0136a0001c0003t0004g0100 | 2 | HG02135.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1523-3268_1523-326 others(32): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(22): Show |
2 | a0001c0003t0001g0093a0001c0003t0001g0129 | 2 | HG01099.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1523-3268_1523-326 others(33): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(25): Show |
1 | a0001c0003t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(36): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(26): Show |
1 | a0001c0003t0001g0062 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(37): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(27): Show |
1 | a0001c0003t0001g0128 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(38): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(31): Show |
1 | a0001c0003t0001g0152 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(42): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
C | CAAAAAAA others(18): Show |
1 | a0001c0003t0001g0097 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1523-3276_1523-327 others(29): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
CA | C | 66 | a0001c0029t0001g0370a0002c0002t0001g0010a0002c0002t0001g0022others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1523-3268delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7815991
|
CAAAAAAA | C | 32 | a0002c0002t0001g0009a0002c0002t0001g0188a0004c0006t0001g0003others(29): Show | 34 | HG00642.hp2 HG00733.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1523-3274_1523-326 others(11): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7815991 | |||||
chr1:7816015
|
A | AAAAAAAA others(12): Show |
1 | a0002c0013t0001g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(23): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7816015 | |||||
chr1:7816015
|
A | AAAAAAAA others(6): Show |
1 | a0016c0027t0005g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1523-3268_1523-326 others(17): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7816015 | |||||
chr1:7816015
|
A | AAAAAAAA others(5): Show |
2 | a0002c0013t0005g0091a0002c0013t0005g0092 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1523-3268_1523-326 others(16): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7816015 | |||||
chr1:7816106
|
T | C | 154 | a0001c0029t0001g0370a0002c0002t0001g0009a0002c0002t0001g0010others(151): Show | 159 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1523-3179T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816106 | ||||||
chr1:7816116
|
AAAG | A | 4 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1523-3163_1523-316 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr1 | 7816116 | |||||
chr1:7816186
|
T | A | 220 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(217): Show | 225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1523-3099T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816186 | ||||||
chr1:7816189
|
A | G | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1523-3096A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816189 | ||||||
chr1:7816278
|
TAA | T | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1523-3006_1523-300 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816278 | ||||||
chr1:7816332
|
T | C | 5 | a0001c0001t0001g0299a0001c0003t0001g0113a0001c0003t0001g0137others(2): Show | 5 | HG03471.hp2 NA18948.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1523-2953T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816332 | ||||||
chr1:7816364
|
A | G | 1 | a0001c0003t0001g0145 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1523-2921A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816364 | ||||||
chr1:7816416
|
G | A | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1523-2869G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816416 | ||||||
chr1:7816463
|
T | C | 13 | a0001c0007t0001g0011a0001c0007t0001g0203a0001c0007t0001g0255others(10): Show | 14 | HG00423.hp2 HG02056.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.1523-2822T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816463 | ||||||
chr1:7816530
|
A | G | 1 | a0001c0001t0001g0002 | 3 | HG02809.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1523-2755A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816530 | ||||||
chr1:7816628
|
A | G | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2657A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816628 | ||||||
chr1:7816629
|
C | CCA | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2656_1523-265 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816629 | ||||||
chr1:7816630
|
A | T | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2655A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816630 | ||||||
chr1:7816631
|
C | T | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2654C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816631 | ||||||
chr1:7816633
|
A | T | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2652A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816633 | ||||||
chr1:7816638
|
T | G | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2647T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816638 | ||||||
chr1:7816639
|
C | A | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2646C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816639 | ||||||
chr1:7816644
|
A | T | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2641A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816644 | ||||||
chr1:7816645
|
GAA | G | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2639_1523-263 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816645 | ||||||
chr1:7816648
|
T | G | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2637T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816648 | ||||||
chr1:7816649
|
G | T | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2636G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816649 | ||||||
chr1:7816651
|
C | T | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523-2634C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816651 | ||||||
chr1:7816663
|
A | T | 1 | a0004c0006t0001g0028 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1523-2622A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816663 | ||||||
chr1:7816946
|
G | A | 1 | a0001c0003t0001g0141 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1523-2339G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816946 | ||||||
chr1:7816948
|
G | A | 216 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(213): Show | 221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.1523-2337G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7816948 | ||||||
chr1:7817343
|
C | T | 2 | a0002c0002t0001g0209a0002c0002t0001g0212 | 2 | HG01123.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1523-1942C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817343 | ||||||
chr1:7817428
|
A | G | 223 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(220): Show | 228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1523-1857A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817428 | ||||||
chr1:7817490
|
T | C | 5 | a0002c0002t0001g0195a0002c0002t0001g0196a0002c0002t0001g0197others(2): Show | 5 | HG02145.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1523-1795T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817490 | ||||||
chr1:7817706
|
G | A | 5 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1523-1579G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817706 | ||||||
chr1:7817718
|
G | C | 1 | a0001c0001t0001g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1523-1567G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817718 | ||||||
chr1:7817727
|
T | C | 1 | a0001c0003t0001g0121 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1523-1558T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817727 | ||||||
chr1:7817740
|
A | T | 3 | a0002c0013t0005g0091a0002c0013t0005g0092a0016c0027t0005g0089 | 3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1523-1545A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817740 | ||||||
chr1:7817846
|
C | T | 1 | a0002c0002t0001g0220 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1523-1439C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817846 | ||||||
chr1:7817874
|
T | C | 62 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1523-1411T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817874 | ||||||
chr1:7817887
|
A | G | 3 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1523-1398A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817887 | ||||||
chr1:7817996
|
A | G | 223 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(220): Show | 228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1523-1289A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7817996 | ||||||
chr1:7818480
|
C | A | 1 | a0002c0002t0012g0200 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1523-805C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818480 | ||||||
chr1:7818487
|
A | G | 223 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(220): Show | 228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1523-798A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818487 | ||||||
chr1:7818508
|
C | T | 9 | a0001c0004t0001g0159a0001c0004t0001g0161a0001c0004t0001g0163others(6): Show | 9 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1523-777C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818508 | ||||||
chr1:7818574
|
A | G | 12 | a0002c0002t0001g0201a0002c0002t0001g0204a0002c0002t0001g0205others(9): Show | 12 | HG00099.hp2 HG01106.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1523-711A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818574 | ||||||
chr1:7818661
|
G | A | 1 | a0001c0003t0001g0152 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1523-624G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818661 | ||||||
chr1:7818902
|
C | T | 2 | a0001c0003t0001g0104a0001c0003t0001g0151 | 2 | NA18959.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1523-383C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818902 | ||||||
chr1:7818905
|
A | G | 1 | a0001c0003t0001g0151 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1523-380A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7818905 | ||||||
chr1:7819003
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(129): Show | 141 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1523-282C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819003 | ||||||
chr1:7819059
|
C | G | 2 | a0009c0015t0001g0054a0009c0015t0001g0055 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1523-226C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819059 | ||||||
chr1:7819070
|
T | G | 223 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(220): Show | 228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1523-215T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819070 | ||||||
chr1:7819108
|
G | A | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1523-177G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819108 | ||||||
chr1:7819141
|
G | C | 2 | a0001c0004t0001g0161a0001c0004t0001g0166 | 2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1523-144G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819141 | ||||||
chr1:7819156
|
T | C | 3 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0377 | 3 | HG01884.hp1 HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1523-129T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819156 | ||||||
chr1:7819262
|
C | T | 24 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(21): Show | 25 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1523-23C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 13/21 | chr1 | 7819262 | ||||||
chr1:7819422
|
T | C | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | splice_donor_variant&intron_variant | HIGH | c.1658+2T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819422 | ||||||
chr1:7819444
|
C | A | 1 | a0004c0006t0001g0039 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1658+24C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819444 | ||||||
chr1:7819461
|
G | A | 1 | a0001c0004t0002g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1658+41G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819461 | ||||||
chr1:7819567
|
C | T | 28 | a0001c0003t0001g0119a0001c0004t0001g0006a0001c0004t0001g0007others(25): Show | 33 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1658+147C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819567 | ||||||
chr1:7819625
|
T | C | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1658+205T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819625 | ||||||
chr1:7819792
|
A | AT | 254 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(251): Show | 270 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.1659-308dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 7819792 | |||||
chr1:7819879
|
G | A | 62 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1659-236G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 14/21 | chr1 | 7819879 | ||||||
chr1:7820312
|
T | C | 12 | a0001c0004t0002g0001a0001c0004t0002g0008a0001c0004t0002g0160others(9): Show | 15 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783+73T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820312 | ||||||
chr1:7820321
|
A | G | 2 | a0009c0015t0001g0054a0009c0015t0001g0055 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1783+82A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820321 | ||||||
chr1:7820365
|
A | G | 1 | a0011c0018t0017g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1784-102A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820365 | ||||||
chr1:7820409
|
A | G | 223 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(220): Show | 228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1784-58A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820409 | ||||||
chr1:7820419
|
C | G | 7 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1784-48C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820419 | ||||||
chr1:7820422
|
G | A | 5 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784-45G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 15/21 | chr1 | 7820422 | ||||||
chr1:7820652
|
G | A | 2 | a0004c0006t0001g0025a0004c0006t0001g0036 | 2 | HG00642.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1957+12G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820652 | ||||||
chr1:7820698
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1957+58G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820698 | ||||||
chr1:7820727
|
C | G | 3 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1957+87C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820727 | ||||||
chr1:7820787
|
T | G | 1 | a0003c0005t0001g0081 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1957+147T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820787 | ||||||
chr1:7820845
|
T | C | 1 | a0013c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1957+205T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820845 | ||||||
chr1:7820958
|
T | C | 4 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187others(1): Show | 4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957+318T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820958 | ||||||
chr1:7820994
|
G | A | 4 | a0004c0006t0001g0026a0004c0006t0001g0029a0004c0006t0001g0030others(1): Show | 4 | HG01109.hp2 HG01433.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957+354G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7820994 | ||||||
chr1:7821154
|
C | T | 1 | a0002c0002t0001g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1957+514C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821154 | ||||||
chr1:7821174
|
C | T | 27 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(24): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1957+534C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821174 | ||||||
chr1:7821190
|
C | T | 5 | a0001c0004t0002g0001a0001c0004t0002g0160a0001c0004t0002g0167others(2): Show | 7 | HG00639.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957+550C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821190 | ||||||
chr1:7821210
|
G | A | 1 | a0002c0002t0012g0200 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1957+570G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821210 | ||||||
chr1:7821255
|
T | A | 1 | a0001c0003t0001g0151 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1957+615T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821255 | ||||||
chr1:7821618
|
C | T | 1 | a0002c0002t0001g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1957+978C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821618 | ||||||
chr1:7821672
|
G | A | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1957+1032G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821672 | ||||||
chr1:7821708
|
A | T | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1957+1068A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821708 | ||||||
chr1:7821720
|
C | T | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1957+1080C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821720 | ||||||
chr1:7821859
|
T | C | 1 | a0002c0012t0001g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1957+1219T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821859 | ||||||
chr1:7821943
|
G | C | 1 | a0001c0001t0001g0325 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1957+1303G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7821943 | ||||||
chr1:7822250
|
A | T | 1 | a0002c0002t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1957+1610A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822250 | ||||||
chr1:7822258
|
AT | A | 217 | a0001c0001t0001g0339a0001c0003t0001g0062a0001c0003t0001g0093others(214): Show | 222 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1957+1633delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 7822258 | |||||
chr1:7822260
|
T | A | 1 | a0003c0005t0001g0084 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1957+1620T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822260 | ||||||
chr1:7822319
|
G | A | 1 | a0001c0003t0001g0111 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1957+1679G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822319 | ||||||
chr1:7822395
|
A | G | 223 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(220): Show | 228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1957+1755A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822395 | ||||||
chr1:7822479
|
C | T | 5 | a0002c0002t0001g0235a0002c0002t0001g0236a0002c0002t0001g0269others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1957+1839C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822479 | ||||||
chr1:7822490
|
T | A | 1 | a0001c0003t0001g0097 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1957+1850T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822490 | ||||||
chr1:7822496
|
G | T | 3 | a0002c0013t0005g0091a0002c0013t0005g0092a0016c0027t0005g0089 | 3 | HG02895.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1957+1856G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822496 | ||||||
chr1:7822976
|
T | C | 62 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1957+2336T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822976 | ||||||
chr1:7822999
|
T | G | 2 | a0004c0006t0001g0034a0004c0006t0001g0043 | 2 | HG00741.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1957+2359T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7822999 | ||||||
chr1:7823127
|
C | G | 1 | a0001c0001t0001g0284 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1957+2487C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823127 | ||||||
chr1:7823132
|
C | T | 4 | a0001c0003t0001g0118a0001c0003t0001g0127a0001c0003t0001g0128others(1): Show | 4 | HG01934.hp2 HG01943.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957+2492C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823132 | ||||||
chr1:7823298
|
A | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(159): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1957+2658A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823298 | ||||||
chr1:7823364
|
C | T | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1957+2724C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823364 | ||||||
chr1:7823400
|
T | C | 83 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(80): Show | 85 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1957+2760T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823400 | ||||||
chr1:7823500
|
G | C | 1 | a0001c0001t0001g0371 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1957+2860G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823500 | ||||||
chr1:7823557
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(125): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1957+2917G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823557 | ||||||
chr1:7823598
|
C | T | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1958-2882C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823598 | ||||||
chr1:7823746
|
T | G | 1 | a0004c0006t0001g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1958-2734T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823746 | ||||||
chr1:7823769
|
G | A | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1958-2711G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823769 | ||||||
chr1:7823774
|
A | G | 220 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(217): Show | 225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1958-2706A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7823774 | ||||||
chr1:7824110
|
A | G | 1 | a0001c0004t0001g0306 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1958-2370A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824110 | ||||||
chr1:7824112
|
G | A | 1 | a0001c0001t0001g0381 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1958-2368G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824112 | ||||||
chr1:7824165
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1958-2315G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824165 | ||||||
chr1:7824343
|
T | G | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1958-2137T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824343 | ||||||
chr1:7824370
|
C | T | 1 | a0002c0002t0001g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1958-2110C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824370 | ||||||
chr1:7824465
|
G | T | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1958-2015G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824465 | ||||||
chr1:7824509
|
C | T | 4 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1958-1971C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824509 | ||||||
chr1:7824520
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(158): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1958-1960T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824520 | ||||||
chr1:7824573
|
T | C | 7 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1958-1907T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824573 | ||||||
chr1:7824632
|
T | C | 6 | a0002c0002t0001g0235a0002c0002t0001g0236a0002c0002t0001g0249others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958-1848T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824632 | ||||||
chr1:7824949
|
G | A | 3 | a0001c0003t0001g0106a0001c0003t0001g0107a0001c0003t0001g0109 | 3 | NA18963.hp1 NA18966.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1958-1531G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7824949 | ||||||
chr1:7825042
|
C | CT | 6 | a0001c0004t0006g0155a0001c0004t0006g0156a0001c0004t0006g0158others(3): Show | 6 | HG00280.hp1 HG01261.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1958-1426dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 7825042 | |||||
chr1:7825294
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(129): Show | 141 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1958-1186A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825294 | ||||||
chr1:7825296
|
A | T | 1 | a0015c0022t0005g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1958-1184A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825296 | ||||||
chr1:7825424
|
A | G | 3 | a0002c0002t0001g0235a0002c0002t0001g0236a0002c0002t0001g0277 | 3 | HG02280.hp1 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1958-1056A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825424 | ||||||
chr1:7825848
|
G | A | 2 | a0003c0005t0001g0005a0003c0005t0001g0154 | 3 | HG02895.hp2 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1958-632G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825848 | ||||||
chr1:7825891
|
C | CAA | 209 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(206): Show | 213 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1958-576_1958-575d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 7825891 | |||||
chr1:7825891
|
C | CAAA | 11 | a0001c0003t0001g0095a0001c0003t0001g0126a0001c0003t0001g0129others(8): Show | 12 | HG01099.hp2 HG01123.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1958-577_1958-575d others(5): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 7825891 | |||||
chr1:7825916
|
C | A | 1 | a0002c0002t0001g0202 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1958-564C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7825916 | ||||||
chr1:7826024
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(158): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1958-456G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826024 | ||||||
chr1:7826056
|
G | C | 74 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(71): Show | 75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1958-424G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826056 | ||||||
chr1:7826057
|
C | T | 74 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(71): Show | 75 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1958-423C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826057 | ||||||
chr1:7826097
|
G | C | 1 | a0002c0002t0001g0061 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1958-383G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826097 | ||||||
chr1:7826281
|
T | A | 1 | a0003c0005t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1958-199T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826281 | ||||||
chr1:7826364
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 142 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1958-116G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826364 | ||||||
chr1:7826429
|
A | G | 1 | a0001c0003t0001g0127 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1958-51A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 16/21 | chr1 | 7826429 | ||||||
chr1:7826746
|
A | G | 5 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2188+36A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 17/21 | chr1 | 7826746 | ||||||
chr1:7826857
|
A | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0341a0001c0001t0001g0342others(1): Show | 6 | HG02809.hp1 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2188+147A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 17/21 | chr1 | 7826857 | ||||||
chr1:7826963
|
G | A | 1 | a0015c0022t0005g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2189-155G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 17/21 | chr1 | 7826963 | ||||||
chr1:7827043
|
C | G | 1 | a0002c0002t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2189-75C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 17/21 | chr1 | 7827043 | ||||||
chr1:7827866
|
A | G | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2886+51A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7827866 | ||||||
chr1:7827949
|
C | T | 10 | a0001c0001t0001g0263a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02056.hp1 HG03834.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.2886+134C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7827949 | ||||||
chr1:7828098
|
T | C | 382 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(379): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.2886+283T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828098 | ||||||
chr1:7828109
|
A | C | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.2886+294A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828109 | ||||||
chr1:7828155
|
A | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.2886+340A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828155 | ||||||
chr1:7828168
|
C | T | 1 | a0002c0002t0001g0242 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2886+353C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828168 | ||||||
chr1:7828228
|
C | T | 2 | a0001c0004t0002g0008a0001c0004t0002g0173 | 3 | HG02258.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2886+413C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828228 | ||||||
chr1:7828378
|
C | T | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.2886+563C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828378 | ||||||
chr1:7828512
|
T | C | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.2886+697T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828512 | ||||||
chr1:7828670
|
G | C | 26 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(23): Show | 31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.2886+855G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7828670 | ||||||
chr1:7829092
|
C | T | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.2887-742C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829092 | ||||||
chr1:7829214
|
A | G | 1 | a0001c0003t0001g0095 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2887-620A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829214 | ||||||
chr1:7829214
|
A | T | 14 | a0001c0001t0001g0264a0001c0007t0001g0011a0001c0007t0001g0203others(11): Show | 15 | HG00423.hp2 HG02056.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.2887-620A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829214 | ||||||
chr1:7829225
|
A | G | 1 | a0004c0006t0001g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2887-609A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829225 | ||||||
chr1:7829318
|
A | C | 382 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(379): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.2887-516A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829318 | ||||||
chr1:7829487
|
G | T | 1 | a0002c0002t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2887-347G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829487 | ||||||
chr1:7829744
|
C | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(280): Show | 300 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.2887-90C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829744 | ||||||
chr1:7829781
|
G | C | 3 | a0002c0002t0001g0215a0002c0002t0001g0237a0002c0002t0001g0238 | 3 | HG00408.hp1 HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.2887-53G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 18/21 | chr1 | 7829781 | ||||||
chr1:7830204
|
A | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(280): Show | 300 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.3214+43A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830204 | ||||||
chr1:7830585
|
A | G | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3214+424A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830585 | ||||||
chr1:7830741
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(125): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.3214+580C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830741 | ||||||
chr1:7830787
|
C | T | 1 | a0003c0005t0001g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3214+626C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830787 | ||||||
chr1:7830896
|
G | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(287): Show | 307 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.3214+735G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7830896 | ||||||
chr1:7831023
|
A | T | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3214+862A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831023 | ||||||
chr1:7831037
|
A | C | 12 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0289others(9): Show | 12 | HG00438.hp2 HG00558.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.3214+876A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831037 | ||||||
chr1:7831318
|
C | T | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3214+1157C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831318 | ||||||
chr1:7831409
|
CT | C | 3 | a0001c0001t0001g0321a0001c0001t0001g0323a0001c0001t0001g0329 | 3 | HG00642.hp1 HG01515.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.3214+1250delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7831409 | |||||
chr1:7831563
|
C | A | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3214+1402C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831563 | ||||||
chr1:7831574
|
A | G | 2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | NA18982.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3214+1413A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831574 | ||||||
chr1:7831737
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(125): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.3214+1576C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831737 | ||||||
chr1:7831789
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3214+1628A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7831789 | ||||||
chr1:7832049
|
T | A | 61 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(58): Show | 64 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.3214+1888T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832049 | ||||||
chr1:7832366
|
CT | C | 96 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0294others(93): Show | 100 | HG00558.hp2 HG00642.hp2 HG00733.hp1 others(97): Show |
intron_variant | MODIFIER | c.3214+2226delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832366 | |||||
chr1:7832366
|
CTT | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(182): Show | 194 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.3214+2225_3214+222 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832366 | |||||
chr1:7832366
|
CTTT | C | 27 | a0001c0001t0001g0290a0001c0004t0001g0006a0001c0004t0001g0007others(24): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.3214+2224_3214+222 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832366 | |||||
chr1:7832393
|
G | A | 383 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(380): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.3214+2232G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832393 | ||||||
chr1:7832499
|
G | A | 92 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(89): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.3214+2338G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832499 | ||||||
chr1:7832563
|
C | T | 87 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(84): Show | 89 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.3214+2402C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832563 | ||||||
chr1:7832619
|
C | T | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3214+2458C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832619 | ||||||
chr1:7832718
|
AT | A | 321 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(318): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.3214+2567delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832718 | |||||
chr1:7832786
|
C | T | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.3214+2625C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832786 | ||||||
chr1:7832811
|
A | G | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.3214+2650A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832811 | ||||||
chr1:7832815
|
C | G | 2 | a0001c0004t0002g0008a0001c0004t0002g0173 | 3 | HG02258.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3214+2654C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832815 | ||||||
chr1:7832837
|
A | AT | 11 | a0001c0001t0001g0313a0001c0001t0001g0362a0001c0004t0002g0160others(8): Show | 11 | HG00639.hp2 HG02559.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.3214+2694dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832837 | |||||
chr1:7832837
|
AT | A | 9 | a0001c0001t0001g0318a0001c0003t0001g0094a0001c0003t0001g0110others(6): Show | 9 | HG01069.hp1 HG01261.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.3214+2694delT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7832837 | |||||
chr1:7832856
|
G | T | 56 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(53): Show | 57 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.3214+2695G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832856 | ||||||
chr1:7832863
|
A | G | 1 | a0015c0022t0005g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3214+2702A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832863 | ||||||
chr1:7832870
|
A | G | 1 | a0003c0005t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3214+2709A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7832870 | ||||||
chr1:7833453
|
A | C | 1 | a0002c0002t0001g0194 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3215-2309A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833453 | ||||||
chr1:7833596
|
A | T | 2 | a0004c0006t0001g0038a0004c0006t0001g0039 | 2 | NA18969.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3215-2166A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833596 | ||||||
chr1:7833631
|
T | C | 1 | a0001c0003t0001g0118 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3215-2131T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833631 | ||||||
chr1:7833637
|
T | G | 1 | a0001c0007t0001g0256 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3215-2125T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833637 | ||||||
chr1:7833753
|
G | A | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3215-2009G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833753 | ||||||
chr1:7833803
|
C | T | 1 | a0003c0005t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3215-1959C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7833803 | ||||||
chr1:7834007
|
C | G | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3215-1755C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834007 | ||||||
chr1:7834067
|
C | T | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3215-1695C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834067 | ||||||
chr1:7834131
|
A | G | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3215-1631A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834131 | ||||||
chr1:7834140
|
A | C | 1 | a0003c0005t0001g0081 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3215-1622A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834140 | ||||||
chr1:7834162
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3215-1600C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834162 | ||||||
chr1:7834167
|
G | A | 2 | a0001c0007t0001g0261a0001c0007t0001g0262 | 2 | HG02056.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.3215-1595G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834167 | ||||||
chr1:7834218
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3215-1544C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834218 | ||||||
chr1:7834399
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3215-1363T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834399 | ||||||
chr1:7834446
|
A | G | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3215-1316A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834446 | ||||||
chr1:7834729
|
A | G | 92 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(89): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.3215-1033A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834729 | ||||||
chr1:7834820
|
T | A | 218 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(215): Show | 223 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.3215-942T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834820 | ||||||
chr1:7834830
|
TAAAC | T | 62 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3215-928_3215-925d others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr1 | 7834830 | |||||
chr1:7834905
|
A | C | 2 | a0004c0006t0001g0027a0004c0006t0001g0028 | 2 | HG02293.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3215-857A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834905 | ||||||
chr1:7834927
|
G | A | 1 | a0014c0019t0001g0320 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3215-835G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834927 | ||||||
chr1:7834941
|
C | G | 1 | a0001c0003t0001g0127 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3215-821C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834941 | ||||||
chr1:7834955
|
C | T | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(11): Show | 16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3215-807C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834955 | ||||||
chr1:7834960
|
G | T | 1 | a0002c0012t0001g0177 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3215-802G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7834960 | ||||||
chr1:7835009
|
A | G | 53 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(50): Show | 56 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.3215-753A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835009 | ||||||
chr1:7835217
|
C | T | 2 | a0001c0003t0001g0130a0001c0003t0001g0131 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3215-545C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835217 | ||||||
chr1:7835218
|
G | A | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.3215-544G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835218 | ||||||
chr1:7835262
|
A | G | 1 | a0003c0005t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3215-500A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835262 | ||||||
chr1:7835358
|
G | T | 30 | a0003c0005t0001g0004a0003c0005t0001g0005a0003c0005t0001g0057others(27): Show | 32 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.3215-404G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835358 | ||||||
chr1:7835449
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3215-313G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835449 | ||||||
chr1:7835512
|
G | A | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3215-250G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 19/21 | chr1 | 7835512 | ||||||
chr1:7836012
|
T | C | 3 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3398+67T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836012 | ||||||
chr1:7836061
|
G | A | 1 | a0001c0001t0018g0375 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3398+116G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836061 | ||||||
chr1:7836122
|
C | T | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.3398+177C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836122 | ||||||
chr1:7836157
|
G | C | 131 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(128): Show | 134 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.3398+212G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836157 | ||||||
chr1:7836211
|
A | T | 1 | a0001c0004t0001g0306 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3398+266A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836211 | ||||||
chr1:7836395
|
T | C | 5 | a0002c0002t0001g0059a0002c0002t0001g0060a0002c0002t0001g0061others(2): Show | 5 | HG02717.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.3398+450T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836395 | ||||||
chr1:7836440
|
A | G | 1 | a0013c0023t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3398+495A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836440 | ||||||
chr1:7836781
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3399-218A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 20/21 | chr1 | 7836781 | ||||||
chr1:7837168
|
G | A | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.3549+19G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837168 | ||||||
chr1:7837197
|
G | A | 2 | a0009c0015t0001g0054a0009c0015t0001g0055 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.3549+48G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837197 | ||||||
chr1:7837280
|
A | G | 1 | a0001c0004t0011g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3549+131A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837280 | ||||||
chr1:7837411
|
G | A | 2 | a0001c0001t0001g0328a0001c0001t0001g0352 | 2 | NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.3549+262G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837411 | ||||||
chr1:7837415
|
T | G | 1 | a0002c0002t0001g0276 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3549+266T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837415 | ||||||
chr1:7837426
|
G | A | 1 | a0015c0022t0005g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3549+277G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837426 | ||||||
chr1:7837489
|
G | A | 1 | a0003c0005t0001g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3549+340G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837489 | ||||||
chr1:7837555
|
A | G | 1 | a0011c0018t0017g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3549+406A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837555 | ||||||
chr1:7837562
|
A | T | 14 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(11): Show | 16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3549+413A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837562 | ||||||
chr1:7837759
|
T | C | 3 | a0002c0012t0001g0177a0002c0012t0001g0178a0002c0012t0001g0179 | 3 | HG02055.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3549+610T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837759 | ||||||
chr1:7837826
|
C | T | 6 | a0002c0002t0001g0059a0002c0002t0001g0060a0002c0002t0001g0061others(3): Show | 6 | HG02257.hp2 HG02717.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.3549+677C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837826 | ||||||
chr1:7837834
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3549+685G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837834 | ||||||
chr1:7837837
|
G | A | 2 | a0001c0001t0001g0337a0001c0001t0001g0388 | 2 | HG01256.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.3549+688G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837837 | ||||||
chr1:7837869
|
C | T | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.3549+720C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837869 | ||||||
chr1:7837928
|
G | A | 51 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(48): Show | 54 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.3549+779G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7837928 | ||||||
chr1:7838046
|
A | G | 3 | a0001c0001t0001g0331a0001c0011t0001g0018a0001c0011t0001g0351 | 4 | NA18980.hp1 NA19011.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.3549+897A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838046 | ||||||
chr1:7838062
|
C | CGT | 133 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 142 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3549+928_3549+929d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7838062 | |||||
chr1:7838095
|
A | G | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3549+946A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838095 | ||||||
chr1:7838678
|
G | A | 124 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(121): Show | 127 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.3549+1529G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838678 | ||||||
chr1:7838715
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3549+1566A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838715 | ||||||
chr1:7838765
|
G | T | 4 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187others(1): Show | 4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.3549+1616G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838765 | ||||||
chr1:7838870
|
A | G | 1 | a0001c0003t0001g0128 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3549+1721A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838870 | ||||||
chr1:7838904
|
G | A | 4 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0274others(1): Show | 5 | HG00733.hp1 HG01168.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.3549+1755G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838904 | ||||||
chr1:7838961
|
GACTT | G | 31 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(28): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.3549+1817_3549+182 others(8): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7838961 | |||||
chr1:7838967
|
C | T | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3549+1818C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7838967 | ||||||
chr1:7839006
|
GA | G | 75 | a0002c0002t0001g0010a0002c0002t0001g0022a0002c0002t0001g0023others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.3549+1858delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839006 | ||||||
chr1:7839009
|
T | A | 1 | a0001c0004t0002g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3549+1860T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839009 | ||||||
chr1:7839016
|
T | C | 1 | a0001c0004t0001g0159 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3549+1867T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839016 | ||||||
chr1:7839138
|
G | T | 2 | a0002c0016t0001g0182a0002c0016t0001g0273 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3549+1989G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839138 | ||||||
chr1:7839166
|
C | G | 2 | a0009c0015t0001g0054a0009c0015t0001g0055 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.3549+2017C>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839166 | ||||||
chr1:7839277
|
A | C | 1 | a0015c0022t0005g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3549+2128A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839277 | ||||||
chr1:7839280
|
C | T | 1 | a0001c0001t0001g0327 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3549+2131C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839280 | ||||||
chr1:7839281
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3549+2132G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839281 | ||||||
chr1:7839438
|
A | G | 1 | a0002c0002t0001g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3549+2289A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839438 | ||||||
chr1:7839476
|
T | G | 1 | a0002c0002t0001g0061 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3549+2327T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839476 | ||||||
chr1:7839485
|
G | A | 1 | a0002c0002t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3549+2336G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839485 | ||||||
chr1:7839617
|
T | C | 4 | a0002c0013t0001g0088a0002c0013t0005g0091a0002c0013t0005g0092others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3549+2468T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839617 | ||||||
chr1:7839676
|
T | C | 2 | a0002c0002t0001g0209a0002c0002t0001g0212 | 2 | HG01123.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.3549+2527T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839676 | ||||||
chr1:7839759
|
C | T | 1 | a0001c0003t0001g0106 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3549+2610C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839759 | ||||||
chr1:7839879
|
G | GACA | 27 | a0003c0005t0001g0004a0003c0005t0001g0063a0003c0005t0001g0064others(24): Show | 28 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.3549+2731_3549+273 others(7): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7839879 | |||||
chr1:7839900
|
C | A | 4 | a0007c0009t0001g0304a0007c0009t0001g0317a0007c0009t0001g0322others(1): Show | 4 | HG01243.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3549+2751C>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7839900 | ||||||
chr1:7840266
|
T | G | 1 | a0001c0007t0001g0256 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3550-2406T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840266 | ||||||
chr1:7840334
|
TA | T | 3 | a0001c0003t0001g0130a0004c0006t0001g0044a0004c0006t0001g0052 | 3 | HG01257.hp1 HG03490.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.3550-2337delA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840334 | ||||||
chr1:7840335
|
A | AT | 17 | a0002c0002t0001g0009a0002c0002t0001g0188a0002c0002t0001g0190others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.3550-2326dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7840335 | |||||
chr1:7840335
|
A | T | 121 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(118): Show | 124 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.3550-2337A>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840335 | ||||||
chr1:7840339
|
T | G | 1 | a0004c0006t0001g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3550-2333T>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840339 | ||||||
chr1:7840470
|
C | T | 1 | a0005c0025t0014g0266 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3550-2202C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840470 | ||||||
chr1:7840498
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3550-2174C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840498 | ||||||
chr1:7840648
|
T | A | 1 | a0001c0001t0018g0375 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3550-2024T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840648 | ||||||
chr1:7840689
|
C | T | 1 | a0002c0002t0001g0277 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3550-1983C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840689 | ||||||
chr1:7840701
|
G | C | 4 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187others(1): Show | 4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.3550-1971G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840701 | ||||||
chr1:7840774
|
A | AT | 8 | a0001c0001t0001g0326a0001c0003t0001g0141a0001c0004t0001g0013others(5): Show | 9 | HG01891.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3550-1885dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7840774 | |||||
chr1:7840887
|
C | T | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3550-1785C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840887 | ||||||
chr1:7840908
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3550-1764A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840908 | ||||||
chr1:7840978
|
G | T | 62 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3550-1694G>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840978 | ||||||
chr1:7840997
|
T | C | 1 | a0002c0002t0001g0248 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3550-1675T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7840997 | ||||||
chr1:7841288
|
A | AT | 100 | a0001c0001t0001g0355a0001c0001t0001g0371a0002c0002t0001g0009others(97): Show | 104 | HG00408.hp2 HG00642.hp2 HG00733.hp1 others(101): Show |
intron_variant | MODIFIER | c.3550-1370dupT | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7841288 | |||||
chr1:7841288
|
A | ATT | 62 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3550-1371_3550-137 others(6): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7841288 | |||||
chr1:7841369
|
A | G | 70 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.3550-1303A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841369 | ||||||
chr1:7841484
|
G | C | 1 | a0017c0026t0001g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3550-1188G>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841484 | ||||||
chr1:7841587
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0372 | 2 | NA18961.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.3550-1085C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841587 | ||||||
chr1:7841697
|
A | G | 2 | a0001c0004t0001g0007a0001c0004t0001g0162 | 3 | NA18946.hp1 NA18956.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3550-975A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841697 | ||||||
chr1:7841785
|
T | C | 2 | a0009c0015t0001g0054a0009c0015t0001g0055 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.3550-887T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841785 | ||||||
chr1:7841826
|
A | G | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3550-846A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841826 | ||||||
chr1:7841828
|
T | C | 63 | a0001c0003t0001g0062a0001c0003t0001g0093a0001c0003t0001g0094others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.3550-844T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841828 | ||||||
chr1:7841935
|
T | C | 384 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(381): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.3550-737T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7841935 | ||||||
chr1:7842129
|
T | A | 1 | a0002c0021t0001g0379 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3550-543T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842129 | ||||||
chr1:7842171
|
A | G | 92 | a0002c0002t0001g0009a0002c0002t0001g0010a0002c0002t0001g0022others(89): Show | 94 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.3550-501A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842171 | ||||||
chr1:7842306
|
G | A | 4 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187others(1): Show | 4 | HG02258.hp1 HG02647.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.3550-366G>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842306 | ||||||
chr1:7842407
|
A | G | 6 | a0002c0002t0001g0235a0002c0002t0001g0236a0002c0002t0001g0249others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3550-265A>G | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842407 | ||||||
chr1:7842414
|
C | T | 27 | a0001c0004t0001g0006a0001c0004t0001g0007a0001c0004t0001g0056others(24): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.3550-258C>T | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842414 | ||||||
chr1:7842499
|
C | CA | 11 | a0001c0004t0002g0001a0001c0004t0002g0160a0001c0004t0002g0167others(8): Show | 13 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.3550-162dupA | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7842499 | |||||
chr1:7842499
|
C | CAA | 30 | a0004c0006t0001g0003a0004c0006t0001g0024a0004c0006t0001g0025others(27): Show | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.3550-163_3550-162d others(4): Show |
PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 7842499 | |||||
chr1:7842511
|
T | A | 2 | a0002c0002t0001g0009a0002c0002t0001g0188 | 3 | HG00733.hp1 HG01168.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.3550-161T>A | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842511 | ||||||
chr1:7842598
|
A | C | 1 | a0002c0002t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3550-74A>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842598 | ||||||
chr1:7842655
|
T | C | 2 | a0001c0001t0001g0019a0010c0031t0001g0019 | 2 | NA18973.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.3550-17T>C | PER3 | ENSG00000049246.15 | transcript | ENST00000377532.8 | protein_coding | 21/21 | chr1 | 7842655 |