geneid | 84808 |
---|---|
ensemblid | ENSG00000187642.10 |
hgncid | 28208 |
symbol | PERM1 |
name | PPARGC1 and ESRR induced regulator, muscle 1 |
refseq_nuc | NM_001394713.1 |
refseq_prot | NP_001381642.1 |
ensembl_nuc | ENST00000433179.4 |
ensembl_prot | ENSP00000414022.3 |
mane_status | MANE Select |
chr | chr1 |
start | 975198 |
end | 982093 |
strand | - |
ver | v1.2 |
region | chr1:975198-982093 |
region5000 | chr1:970198-987093 |
regionname0 | PERM1_chr1_975198_982093 |
regionname5000 | PERM1_chr1_970198_987093 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 790 | 211 | 22 | 44 | 113 | 6 | 25 | 77 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002 | 0/0 | 790 | 85 | 45 | 18 | 12 | 2 | 8 | 10 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003 | 0/0 | 790 | 49 | 11 | 11 | 14 | 5 | 8 | 11 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0004 | 0/0 | 790 | 22 | 6 | 2 | 14 | 0 | 0 | 11 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0005 | 1/0 | 790 | 11 | 7 | 1 | 0 | 1 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0006 | 0/0 | 790 | 6 | 1 | 2 | 0 | 2 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0007 | 0/0 | 790 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0008 | 0/0 | 790 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0009 | 0/0 | 790 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0010 | 0/0 | 790 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0011 | 0/0 | 790 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0012 | 0/0 | 790 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0013 | 0/0 | 790 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0014 | 0/0 | 790 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0015 | 0/0 | 790 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0016 | 0/0 | 790 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0017 | 0/0 | 790 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0018 | 0/0 | 790 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0019 | 0/0 | 790 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0020 | 0/0 | 790 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0021 | 0/0 | 790 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0022 | 0/0 | 790 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0023 | 0/0 | 790 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2373 | 192 | 19 | 34 | 109 | 6 | 23 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0002 | 0/0 | 2373 | 60 | 20 | 18 | 12 | 2 | 8 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0003 | 0/0 | 2373 | 43 | 11 | 8 | 11 | 5 | 8 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0004 | 0/0 | 2373 | 20 | 5 | 2 | 13 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0005 | 0/0 | 2373 | 17 | 17 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0006 | 1/0 | 2373 | 11 | 7 | 1 | 0 | 1 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0007 | 0/0 | 2373 | 10 | 0 | 7 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0008 | 0/0 | 2373 | 6 | 1 | 2 | 0 | 2 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0009 | 0/0 | 2373 | 5 | 5 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0010 | 0/0 | 2373 | 4 | 0 | 0 | 4 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0011 | 0/0 | 2373 | 3 | 3 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0012 | 0/0 | 2373 | 3 | 0 | 0 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0013 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0014 | 0/0 | 2373 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0015 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0016 | 0/0 | 2373 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0017 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0018 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0019 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0020 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0021 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0022 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0023 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0024 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0025 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0026 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0027 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0028 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0029 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0030 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0031 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0032 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0033 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0034 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0035 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0036 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0037 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0038 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0039 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0040 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0041 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
c0042 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1148 | 159 | 11 | 36 | 80 | 6 | 25 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0002 | 0/0 | 1148 | 106 | 36 | 30 | 30 | 2 | 8 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0003 | 0/0 | 1148 | 48 | 8 | 3 | 34 | 2 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0004 | 0/0 | 1148 | 48 | 13 | 9 | 13 | 5 | 8 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0005 | 1/0 | 1148 | 23 | 19 | 2 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0006 | 0/0 | 1148 | 4 | 0 | 0 | 4 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0007 | 0/0 | 1148 | 3 | 0 | 0 | 0 | 0 | 3 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0008 | 0/0 | 1148 | 3 | 3 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0009 | 0/0 | 1148 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0010 | 0/0 | 1148 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0011 | 0/0 | 1148 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0012 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0013 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0014 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0015 | 0/0 | 1148 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0016 | 0/0 | 1148 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0017 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0018 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0019 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0020 | 0/0 | 1116 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
t0021 | 0/0 | 1148 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 21 | 0 | 0 | 19 | 2 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0002 | 0/0 | 18 | 0 | 6 | 8 | 0 | 4 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0003 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0004 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0005 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0006 | 0/0 | 8 | 0 | 3 | 3 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0008 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0009 | 0/0 | 5 | 0 | 0 | 2 | 1 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0010 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0011 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0014 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0041 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2373 | 192 | 19 | 34 | 109 | 6 | 23 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0007 | 0/0 | 2373 | 10 | 0 | 7 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0015 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0020 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0028 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0030 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0031 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0032 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0034 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0042 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0002 | 0/0 | 2373 | 60 | 20 | 18 | 12 | 2 | 8 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0005 | 0/0 | 2373 | 17 | 17 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0009 | 0/0 | 2373 | 5 | 5 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0011 | 0/0 | 2373 | 3 | 3 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0003 | 0/0 | 2373 | 43 | 11 | 8 | 11 | 5 | 8 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0016 | 0/0 | 2373 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0018 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0022 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0026 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0036 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0004c0004 | 0/0 | 2373 | 20 | 5 | 2 | 13 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0004c0021 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0004c0025 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0005c0006 | 1/0 | 2373 | 11 | 7 | 1 | 0 | 1 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0006c0008 | 0/0 | 2373 | 6 | 1 | 2 | 0 | 2 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0007c0010 | 0/0 | 2373 | 4 | 0 | 0 | 4 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0008c0012 | 0/0 | 2373 | 3 | 0 | 0 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0009c0014 | 0/0 | 2373 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0010c0013 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0011c0041 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0012c0019 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0013c0040 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0014c0039 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0015c0038 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0016c0037 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0017c0029 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0018c0033 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0019c0035 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0020c0023 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0021c0024 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0022c0027 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0023c0017 | 0/0 | 2373 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3520 | 124 | 6 | 23 | 70 | 4 | 20 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0002 | 0/0 | 3520 | 9 | 1 | 8 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0003 | 0/0 | 3520 | 47 | 8 | 3 | 33 | 2 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0006 | 0/0 | 3520 | 4 | 0 | 0 | 4 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0007 | 0/0 | 3520 | 2 | 0 | 0 | 0 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0010 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0011 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0012 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0013 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0014 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0001t0017 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0007t0001 | 0/0 | 3520 | 10 | 0 | 7 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0015t0002 | 0/0 | 3520 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0020t0002 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0028t0004 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0030t0001 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0031t0001 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0032t0007 | 0/0 | 3520 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0034t0001 | 0/0 | 3520 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0001c0042t0003 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0002t0001 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0002t0002 | 0/0 | 3520 | 59 | 19 | 18 | 12 | 2 | 8 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0005t0004 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0005t0005 | 0/0 | 3520 | 12 | 12 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0005t0008 | 0/0 | 3520 | 3 | 3 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0005t0009 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0009t0002 | 0/0 | 3520 | 5 | 5 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0002c0011t0002 | 0/0 | 3520 | 3 | 3 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0003t0001 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0003t0004 | 0/0 | 3520 | 41 | 11 | 7 | 11 | 5 | 7 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0003t0020 | 0/0 | 3488 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0016t0004 | 0/0 | 3520 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0018t0001 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0022t0004 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0026t0002 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0003c0036t0021 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0004c0004t0001 | 0/0 | 3520 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0004c0004t0002 | 0/0 | 3520 | 17 | 3 | 2 | 12 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0004c0004t0015 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0004c0021t0002 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0004c0025t0004 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0005c0006t0004 | 0/0 | 3520 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0005c0006t0005 | 1/0 | 3520 | 10 | 7 | 1 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0006c0008t0001 | 0/0 | 3520 | 6 | 1 | 2 | 0 | 2 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0007c0010t0001 | 0/0 | 3520 | 4 | 0 | 0 | 4 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0008c0012t0002 | 0/0 | 3520 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0008c0012t0016 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0009c0014t0002 | 0/0 | 3520 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0010c0013t0018 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0010c0013t0019 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0011c0041t0001 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0012c0019t0001 | 0/0 | 3520 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0013c0040t0005 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0014c0039t0002 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0015c0038t0001 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0016c0037t0009 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0017c0029t0001 | 0/0 | 3520 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0018c0033t0001 | 0/0 | 3520 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0019c0035t0001 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0020c0023t0002 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0021c0024t0002 | 0/0 | 3520 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0022c0027t0002 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
a0023c0017t0001 | 0/0 | 3520 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | copy fasta | chr1 | 970198 | 987093 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 18 | 0 | 6 | 8 | 0 | 4 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0003 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0041 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0002g0008 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0001 | 0/0 | 21 | 0 | 0 | 19 | 2 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0006g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0007g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0011g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0012g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0013g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0014g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0001t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0007t0001g0005 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0007t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0015t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0020t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0028t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0030t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0031t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0032t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0034t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0001c0042t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0006 | 0/0 | 8 | 0 | 3 | 3 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0010 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0011 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0008g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0005t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0009t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0009t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0009t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0009t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0009t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0011t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0002c0011t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0009 | 0/0 | 5 | 0 | 0 | 2 | 1 | 2 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0014 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0003t0020g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0016t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0016t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0018t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0022t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0026t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0003c0036t0021g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0002g0004 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0004t0015g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0021t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0004c0025t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0005c0006t0005g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0006c0008t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0006c0008t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0006c0008t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0006c0008t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0006c0008t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0006c0008t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0007c0010t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0007c0010t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0007c0010t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0008c0012t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0008c0012t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0008c0012t0016g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0009c0014t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0009c0014t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0010c0013t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0010c0013t0019g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0011c0041t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0012c0019t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0013c0040t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0014c0039t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0015c0038t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0016c0037t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0017c0029t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0018c0033t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0019c0035t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0020c0023t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0021c0024t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0022c0027t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
a0023c0017t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0006 | c0008 | t0001 | g0090 | EUR | GBR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0011 | EUR | GBR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00140 | hp2 | a0003 | c0003 | t0004 | g0026 | EUR | GBR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00280 | hp2 | a0006 | c0008 | t0001 | g0088 | EUR | FIN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00323 | hp1 | a0003 | c0003 | t0004 | g0015 | EUR | FIN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00408 | hp2 | a0004 | c0004 | t0002 | g0042 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00423 | hp1 | a0001 | c0042 | t0003 | g0205 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00423 | hp2 | a0001 | c0001 | t0010 | g0147 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00558 | hp2 | a0003 | c0003 | t0004 | g0024 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0044 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00639 | hp1 | a0006 | c0008 | t0001 | g0089 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00673 | hp2 | a0004 | c0004 | t0002 | g0004 | EAS | CHS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00733 | hp1 | a0017 | c0029 | t0001 | g0086 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00735 | hp1 | a0003 | c0003 | t0004 | g0023 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00735 | hp2 | a0003 | c0003 | t0004 | g0026 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00738 | hp2 | a0001 | c0028 | t0004 | g0080 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00741 | hp1 | a0013 | c0040 | t0005 | g0234 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG00741 | hp2 | a0003 | c0003 | t0004 | g0015 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0247 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0249 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0250 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01109 | hp1 | a0003 | c0003 | t0004 | g0021 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01167 | hp1 | a0003 | c0003 | t0004 | g0022 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01167 | hp2 | a0001 | c0007 | t0001 | g0005 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01169 | hp1 | a0001 | c0007 | t0001 | g0005 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01192 | hp2 | a0001 | c0030 | t0001 | g0096 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01243 | hp1 | a0003 | c0003 | t0001 | g0259 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01243 | hp2 | a0003 | c0018 | t0001 | g0237 | AMR | PUR | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01256 | hp2 | a0003 | c0022 | t0004 | g0077 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01257 | hp1 | a0003 | c0003 | t0004 | g0025 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01346 | hp1 | a0003 | c0003 | t0004 | g0022 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01358 | hp2 | a0004 | c0004 | t0002 | g0004 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01433 | hp1 | a0005 | c0006 | t0005 | g0218 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01433 | hp2 | a0006 | c0008 | t0001 | g0085 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01516 | hp1 | a0003 | c0003 | t0004 | g0009 | EUR | IBS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01517 | hp2 | a0003 | c0003 | t0004 | g0014 | EUR | IBS | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01884 | hp1 | a0002 | c0005 | t0009 | g0190 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01891 | hp1 | a0005 | c0006 | t0005 | g0217 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01891 | hp2 | a0003 | c0003 | t0004 | g0024 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01928 | hp2 | a0001 | c0007 | t0001 | g0005 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01943 | hp1 | a0004 | c0004 | t0002 | g0004 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01943 | hp2 | a0001 | c0007 | t0001 | g0005 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01975 | hp1 | a0001 | c0007 | t0001 | g0005 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01975 | hp2 | a0001 | c0007 | t0001 | g0093 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0253 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01978 | hp2 | a0001 | c0007 | t0001 | g0005 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0240 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02055 | hp1 | a0003 | c0003 | t0004 | g0055 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02055 | hp2 | a0014 | c0039 | t0002 | g0265 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02074 | hp1 | a0003 | c0003 | t0004 | g0068 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02080 | hp1 | a0007 | c0010 | t0001 | g0027 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02145 | hp1 | a0010 | c0013 | t0018 | g0209 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02145 | hp2 | a0002 | c0011 | t0002 | g0238 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02155 | hp1 | a0003 | c0003 | t0004 | g0073 | EAS | CDX | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02155 | hp2 | a0004 | c0021 | t0002 | g0084 | EAS | CDX | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02257 | hp1 | a0002 | c0005 | t0005 | g0045 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02257 | hp2 | a0001 | c0001 | t0017 | g0208 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02258 | hp1 | a0005 | c0006 | t0005 | g0219 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02258 | hp2 | a0005 | c0006 | t0005 | g0214 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02273 | hp1 | a0001 | c0020 | t0002 | g0083 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02280 | hp1 | a0002 | c0005 | t0005 | g0225 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02280 | hp2 | a0001 | c0001 | t0014 | g0116 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02451 | hp1 | a0004 | c0004 | t0001 | g0196 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02451 | hp2 | a0002 | c0005 | t0005 | g0045 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02615 | hp1 | a0002 | c0005 | t0005 | g0229 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02615 | hp2 | a0002 | c0005 | t0005 | g0233 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02622 | hp2 | a0002 | c0009 | t0002 | g0261 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0252 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02630 | hp2 | a0002 | c0005 | t0008 | g0046 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02647 | hp1 | a0005 | c0006 | t0005 | g0216 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02647 | hp2 | a0003 | c0003 | t0004 | g0065 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02683 | hp1 | a0001 | c0032 | t0007 | g0170 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02698 | hp1 | a0018 | c0033 | t0001 | g0187 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02717 | hp1 | a0004 | c0004 | t0002 | g0198 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02723 | hp1 | a0002 | c0005 | t0005 | g0228 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02723 | hp2 | a0016 | c0037 | t0009 | g0059 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0248 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02738 | hp1 | a0001 | c0034 | t0001 | g0188 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0056 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02809 | hp2 | a0003 | c0003 | t0004 | g0236 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02818 | hp1 | a0003 | c0003 | t0004 | g0071 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02886 | hp2 | a0004 | c0004 | t0002 | g0193 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02896 | hp1 | a0002 | c0005 | t0005 | g0223 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02896 | hp2 | a0002 | c0011 | t0002 | g0047 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02897 | hp2 | a0002 | c0011 | t0002 | g0047 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02922 | hp1 | a0002 | c0005 | t0005 | g0232 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02970 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02970 | hp2 | a0005 | c0006 | t0005 | g0212 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02976 | hp2 | a0001 | c0015 | t0002 | g0043 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03041 | hp1 | a0002 | c0005 | t0005 | g0226 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03041 | hp2 | a0002 | c0009 | t0002 | g0260 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03098 | hp1 | a0002 | c0005 | t0005 | g0231 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03098 | hp2 | a0002 | c0009 | t0002 | g0262 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03139 | hp2 | a0001 | c0015 | t0002 | g0043 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0242 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0113 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03209 | hp2 | a0002 | c0005 | t0005 | g0230 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03225 | hp1 | a0022 | c0027 | t0002 | g0058 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03225 | hp2 | a0010 | c0013 | t0019 | g0210 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0246 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03486 | hp2 | a0003 | c0003 | t0004 | g0072 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03490 | hp1 | a0006 | c0008 | t0001 | g0087 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03491 | hp1 | a0003 | c0003 | t0004 | g0009 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03492 | hp2 | a0003 | c0003 | t0004 | g0009 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03516 | hp1 | a0004 | c0004 | t0001 | g0195 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03540 | hp1 | a0003 | c0003 | t0004 | g0067 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03540 | hp2 | a0002 | c0005 | t0004 | g0224 | AFR | GWD | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0054 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03579 | hp2 | a0001 | c0031 | t0001 | g0097 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03654 | hp1 | a0003 | c0003 | t0004 | g0025 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03669 | hp1 | a0003 | c0003 | t0004 | g0023 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0034 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03710 | hp1 | a0003 | c0003 | t0020 | g0070 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03710 | hp2 | a0003 | c0003 | t0004 | g0051 | SAS | PJL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03834 | hp2 | a0001 | c0001 | t0007 | g0034 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03927 | hp2 | a0023 | c0017 | t0001 | g0081 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0049 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04184 | hp1 | a0003 | c0003 | t0004 | g0078 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04184 | hp2 | a0003 | c0003 | t0004 | g0079 | SAS | BEB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04204 | hp2 | a0012 | c0019 | t0001 | g0082 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0258 | SAS | STU | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18522 | hp1 | a0002 | c0005 | t0005 | g0222 | AFR | YRI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18522 | hp2 | a0002 | c0009 | t0002 | g0264 | AFR | YRI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18612 | hp2 | a0007 | c0010 | t0001 | g0027 | EAS | CHB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18906 | hp1 | a0003 | c0003 | t0004 | g0021 | AFR | YRI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18939 | hp1 | a0003 | c0003 | t0004 | g0064 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18939 | hp2 | a0007 | c0010 | t0001 | g0094 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18943 | hp2 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18945 | hp1 | a0001 | c0007 | t0001 | g0005 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18948 | hp2 | a0001 | c0007 | t0001 | g0005 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18950 | hp1 | a0003 | c0003 | t0004 | g0009 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18952 | hp1 | a0007 | c0010 | t0001 | g0095 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18954 | hp1 | a0004 | c0004 | t0002 | g0004 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18954 | hp2 | a0009 | c0014 | t0002 | g0199 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18957 | hp2 | a0021 | c0024 | t0002 | g0239 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18959 | hp2 | a0003 | c0016 | t0004 | g0076 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18961 | hp2 | a0015 | c0038 | t0001 | g0203 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18962 | hp2 | a0003 | c0016 | t0004 | g0075 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18965 | hp2 | a0003 | c0003 | t0004 | g0014 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18971 | hp2 | a0019 | c0035 | t0001 | g0189 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18973 | hp2 | a0011 | c0041 | t0001 | g0204 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18974 | hp1 | a0008 | c0012 | t0002 | g0202 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18975 | hp1 | a0009 | c0014 | t0002 | g0200 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18977 | hp1 | a0003 | c0003 | t0004 | g0061 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18980 | hp1 | a0004 | c0004 | t0002 | g0004 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18980 | hp2 | a0003 | c0003 | t0004 | g0009 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18983 | hp1 | a0001 | c0001 | t0011 | g0110 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18988 | hp2 | a0008 | c0012 | t0002 | g0053 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18998 | hp1 | a0004 | c0004 | t0002 | g0192 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19000 | hp2 | a0003 | c0003 | t0004 | g0062 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19005 | hp2 | a0004 | c0004 | t0002 | g0004 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19010 | hp1 | a0004 | c0004 | t0002 | g0004 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19011 | hp1 | a0004 | c0004 | t0002 | g0042 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | LWK | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19030 | hp2 | a0002 | c0005 | t0008 | g0227 | AFR | LWK | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | LWK | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | LWK | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19054 | hp2 | a0003 | c0003 | t0004 | g0014 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19056 | hp2 | a0004 | c0004 | t0015 | g0197 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19059 | hp1 | a0008 | c0012 | t0016 | g0201 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19068 | hp1 | a0004 | c0004 | t0002 | g0004 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19070 | hp1 | a0003 | c0003 | t0004 | g0063 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19075 | hp1 | a0001 | c0007 | t0001 | g0092 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19075 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19078 | hp2 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19079 | hp2 | a0004 | c0004 | t0002 | g0004 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19081 | hp1 | a0004 | c0004 | t0002 | g0194 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19081 | hp2 | a0004 | c0004 | t0002 | g0004 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19082 | hp1 | a0003 | c0036 | t0021 | g0074 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19240 | hp1 | a0020 | c0023 | t0002 | g0052 | AFR | YRI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20129 | hp1 | a0002 | c0009 | t0002 | g0263 | AFR | ASW | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0255 | EUR | TSI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20805 | hp1 | a0003 | c0003 | t0004 | g0015 | EUR | TSI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20805 | hp2 | a0005 | c0006 | t0005 | g0211 | EUR | TSI | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20905 | hp1 | a0005 | c0006 | t0004 | g0220 | SAS | GIH | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG01123 | hp2 | a0003 | c0026 | t0002 | g0251 | AMR | CLM | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02486 | hp2 | a0006 | c0008 | t0001 | g0091 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02559 | hp1 | a0005 | c0006 | t0005 | g0213 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG02559 | hp2 | a0003 | c0003 | t0004 | g0069 | AFR | ACB | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03471 | hp1 | a0004 | c0025 | t0004 | g0060 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | MSL | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG06807 | hp1 | a0005 | c0006 | t0005 | g0215 | AFR | USA | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0245 | AFR | USA | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20300 | hp1 | a0004 | c0004 | t0002 | g0191 | AFR | USA | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA20300 | hp2 | a0002 | c0005 | t0008 | g0046 | AFR | USA | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA21309 | hp1 | a0001 | c0001 | t0013 | g0115 | AFR | LWK | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
NA21309 | hp2 | a0003 | c0003 | t0004 | g0066 | AFR | LWK | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0163 | REF | REF | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
homoSapiens_grch38 | hp1 | a0005 | c0006 | t0005 | g0221 | REF | REF | PERM1_chr1_970198_987093 | PERM1 | chr1 | 970198 | 987093 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:976215
|
A | G | 13 | a0001a0003a0004others(10): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
missense_variant | MODERATE | c.2330T>C | p.Val777Ala | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 2503/3520 | 2330/2373 | 777/790 | chr1 | 976215 | ||
chr1:978953
|
C | G | 12 | a0001a0004a0006others(9): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
missense_variant | MODERATE | c.2077G>C | p.Glu693Gln | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 2250/3520 | 2077/2373 | 693/790 | chr1 | 978953 | ||
chr1:979034
|
C | T | 1 | a0021 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.1996G>A | p.Gly666Arg | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 2169/3520 | 1996/2373 | 666/790 | chr1 | 979034 | ||
chr1:979099
|
G | C | 1 | a0018 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1931C>G | p.Pro644Arg | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 2104/3520 | 1931/2373 | 644/790 | chr1 | 979099 | ||
chr1:979141
|
C | T | 1 | a0020 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1889G>A | p.Arg630Gln | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 2062/3520 | 1889/2373 | 630/790 | chr1 | 979141 | ||
chr1:979182
|
G | C | 1 | a0022 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1848C>G | p.Cys616Trp | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 2021/3520 | 1848/2373 | 616/790 | chr1 | 979182 | ||
chr1:979192
|
G | A | 1 | a0009 | 2 | NA18954.hp2 NA18975.hp1 |
missense_variant | MODERATE | c.1838C>T | p.Pro613Leu | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 2011/3520 | 1838/2373 | 613/790 | chr1 | 979192 | ||
chr1:979369
|
C | T | 1 | a0007 | 4 | HG02080.hp1 NA18612.hp2 NA18939.hp2 others(1): Show |
missense_variant | MODERATE | c.1661G>A | p.Arg554Gln | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1834/3520 | 1661/2373 | 554/790 | chr1 | 979369 | ||
chr1:979385
|
G | A | 1 | a0019 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.1645C>T | p.Arg549Trp | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1818/3520 | 1645/2373 | 549/790 | chr1 | 979385 | ||
chr1:979418
|
G | C | 1 | a0008 | 3 | NA18974.hp1 NA18988.hp2 NA19059.hp1 |
missense_variant | MODERATE | c.1612C>G | p.Pro538Ala | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1785/3520 | 1612/2373 | 538/790 | chr1 | 979418 | ||
chr1:979459
|
C | T | 2 | a0006a0017 | 7 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(4): Show |
missense_variant | MODERATE | c.1571G>A | p.Arg524Gln | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1744/3520 | 1571/2373 | 524/790 | chr1 | 979459 | ||
chr1:979472
|
G | C | 9 | a0001a0006a0007others(6): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
missense_variant | MODERATE | c.1558C>G | p.Gln520Glu | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1731/3520 | 1558/2373 | 520/790 | chr1 | 979472 | ||
chr1:979496
|
T | C | 21 | a0001a0002a0003others(18): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
missense_variant | MODERATE | c.1534A>G | p.Ser512Gly | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1707/3520 | 1534/2373 | 512/790 | chr1 | 979496 | ||
chr1:980110
|
G | A | 1 | a0016 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.920C>T | p.Pro307Leu | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1093/3520 | 920/2373 | 307/790 | chr1 | 980110 | ||
chr1:980185
|
G | A | 1 | a0015 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.845C>T | p.Thr282Met | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1018/3520 | 845/2373 | 282/790 | chr1 | 980185 | ||
chr1:980218
|
G | A | 1 | a0014 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.812C>T | p.Thr271Ile | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 985/3520 | 812/2373 | 271/790 | chr1 | 980218 | ||
chr1:980234
|
T | A | 1 | a0013 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.796A>T | p.Thr266Ser | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 969/3520 | 796/2373 | 266/790 | chr1 | 980234 | ||
chr1:980497
|
C | T | 1 | a0012 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.533G>A | p.Arg178Gln | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 706/3520 | 533/2373 | 178/790 | chr1 | 980497 | ||
chr1:980584
|
G | A | 1 | a0011 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.446C>T | p.Pro149Leu | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 619/3520 | 446/2373 | 149/790 | chr1 | 980584 | ||
chr1:980779
|
G | T | 1 | a0010 | 2 | HG02145.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.251C>A | p.Pro84Gln | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 424/3520 | 251/2373 | 84/790 | chr1 | 980779 | ||
chr1:980972
|
C | G | 1 | a0023 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.58G>C | p.Ala20Pro | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 231/3520 | 58/2373 | 20/790 | chr1 | 980972 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:976536
|
C | T | 8 | a0001c0032a0002c0002a0002c0009others(5): Show | 73 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(70): Show |
synonymous_variant | LOW | c.2238G>A | p.Arg746Arg | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 3/4 | 2411/3520 | 2238/2373 | 746/790 | chr1 | 976536 | ||
chr1:978945
|
C | T | 1 | a0010c0013 | 2 | HG02145.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.2085G>A | p.Ala695Ala | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 2258/3520 | 2085/2373 | 695/790 | chr1 | 978945 | ||
chr1:978996
|
G | T | 1 | a0001c0031 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.2034C>A | p.Val678Val | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 2207/3520 | 2034/2373 | 678/790 | chr1 | 978996 | ||
chr1:979230
|
C | T | 2 | a0002c0011a0003c0022 | 4 | HG01256.hp2 HG02145.hp2 HG02896.hp2 others(1): Show |
synonymous_variant | LOW | c.1800G>A | p.Ala600Ala | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1973/3520 | 1800/2373 | 600/790 | chr1 | 979230 | ||
chr1:979338
|
G | C | 1 | a0016c0037 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1692C>G | p.Pro564Pro | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1865/3520 | 1692/2373 | 564/790 | chr1 | 979338 | ||
chr1:979347
|
G | T | 1 | a0001c0030 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.1683C>A | p.Arg561Arg | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1856/3520 | 1683/2373 | 561/790 | chr1 | 979347 | ||
chr1:979355
|
G | A | 1 | a0001c0034 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1675C>T | p.Leu559Leu | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1848/3520 | 1675/2373 | 559/790 | chr1 | 979355 | ||
chr1:979425
|
G | A | 1 | a0002c0009 | 5 | HG02622.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.1605C>T | p.His535His | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1778/3520 | 1605/2373 | 535/790 | chr1 | 979425 | ||
chr1:979434
|
A | G | 1 | a0001c0007 | 10 | HG01167.hp2 HG01169.hp1 HG01928.hp2 others(7): Show |
synonymous_variant | LOW | c.1596T>C | p.Thr532Thr | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1769/3520 | 1596/2373 | 532/790 | chr1 | 979434 | ||
chr1:979560
|
T | C | 17 | a0001c0001a0001c0007a0001c0015others(14): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
synonymous_variant | LOW | c.1470A>G | p.Ala490Ala | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1643/3520 | 1470/2373 | 490/790 | chr1 | 979560 | ||
chr1:979578
|
G | A | 1 | a0003c0036 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.1452C>T | p.Pro484Pro | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1625/3520 | 1452/2373 | 484/790 | chr1 | 979578 | ||
chr1:979847
|
A | G | 39 | a0001c0001a0001c0007a0001c0015others(36): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
synonymous_variant | LOW | c.1183T>C | p.Leu395Leu | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1356/3520 | 1183/2373 | 395/790 | chr1 | 979847 | ||
chr1:979884
|
G | A | 5 | a0004c0004a0004c0021a0008c0012others(2): Show | 28 | HG00408.hp2 HG00673.hp2 HG01358.hp2 others(25): Show |
synonymous_variant | LOW | c.1146C>T | p.Ser382Ser | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1319/3520 | 1146/2373 | 382/790 | chr1 | 979884 | ||
chr1:980019
|
C | T | 1 | a0010c0013 | 2 | HG02145.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.1011G>A | p.Pro337Pro | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1184/3520 | 1011/2373 | 337/790 | chr1 | 980019 | ||
chr1:980163
|
T | C | 1 | a0001c0015 | 2 | HG02976.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.867A>G | p.Pro289Pro | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 1040/3520 | 867/2373 | 289/790 | chr1 | 980163 | ||
chr1:980214
|
C | T | 1 | a0004c0021 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.816G>A | p.Pro272Pro | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 989/3520 | 816/2373 | 272/790 | chr1 | 980214 | ||
chr1:980406
|
C | G | 1 | a0001c0020 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.624G>C | p.Leu208Leu | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 797/3520 | 624/2373 | 208/790 | chr1 | 980406 | ||
chr1:980634
|
C | T | 1 | a0003c0018 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.396G>A | p.Ala132Ala | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 569/3520 | 396/2373 | 132/790 | chr1 | 980634 | ||
chr1:980796
|
G | A | 1 | a0001c0042 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.234C>T | p.Asp78Asp | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 407/3520 | 234/2373 | 78/790 | chr1 | 980796 | ||
chr1:980967
|
G | A | 1 | a0003c0016 | 2 | NA18959.hp2 NA18962.hp2 |
synonymous_variant | LOW | c.63C>T | p.Thr21Thr | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 236/3520 | 63/2373 | 21/790 | chr1 | 980967 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:975491
|
G | A | 1 | a0001c0001t0014 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 681 | chr1 | 975491 | |||||
chr1:975523
|
T | C | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
3_prime_UTR_variant | MODIFIER | c.*649A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 649 | chr1 | 975523 | |||||
chr1:975552
|
T | A | 1 | a0004c0004t0015 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*620A>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 620 | chr1 | 975552 | |||||
chr1:975555
|
G | A | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(18): Show | 158 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*617C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 617 | chr1 | 975555 | |||||
chr1:975698
|
CTGCCTCT others(25): Show |
C | 1 | a0003c0003t0020 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442_*473delAGACAC others(26): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 442 | chr1 | 975698 | |||||
chr1:975721
|
C | T | 6 | a0001c0001t0003a0001c0001t0011a0001c0001t0013others(3): Show | 54 | HG00423.hp1 HG00609.hp1 HG00642.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*451G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 451 | chr1 | 975721 | |||||
chr1:975749
|
G | A | 1 | a0003c0036t0021 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 423 | chr1 | 975749 | |||||
chr1:975801
|
G | A | 2 | a0001c0001t0007a0001c0032t0007 | 3 | HG02683.hp1 HG03704.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*371C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 371 | chr1 | 975801 | |||||
chr1:975884
|
C | T | 1 | a0001c0001t0012 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*288G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 288 | chr1 | 975884 | |||||
chr1:975921
|
C | T | 1 | a0001c0001t0011 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*251G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 251 | chr1 | 975921 | |||||
chr1:976038
|
A | C | 2 | a0010c0013t0018a0010c0013t0019 | 2 | HG02145.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*134T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 134 | chr1 | 976038 | |||||
chr1:976047
|
C | A | 1 | a0008c0012t0016 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 125 | chr1 | 976047 | |||||
chr1:976132
|
C | G | 1 | a0001c0001t0010 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*40G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 4/4 | 40 | chr1 | 976132 | |||||
chr1:981119
|
G | A | 1 | a0001c0001t0006 | 4 | HG00408.hp1 HG00609.hp2 NA18943.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-90C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 90 | chr1 | 981119 | |||||
chr1:981154
|
C | T | 1 | a0010c0013t0018 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-125G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 125 | chr1 | 981154 | |||||
chr1:981157
|
G | A | 1 | a0001c0001t0017 | 1 | HG02257.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | chr1 | 981157 | ||||||
chr1:981169
|
A | G | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
5_prime_UTR_variant | MODIFIER | c.-140T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/4 | 140 | chr1 | 981169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:976278
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2276-9C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 3/3 | chr1 | 976278 | ||||||
chr1:976389
|
G | T | 1 | a0003c0003t0004g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2275+110C>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 3/3 | chr1 | 976389 | ||||||
chr1:976448
|
C | T | 1 | a0016c0037t0009g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2275+51G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 3/3 | chr1 | 976448 | ||||||
chr1:976642
|
CTTCAGCC others(5): Show |
C | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-30_2150-19del others(12): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976642 | ||||||
chr1:976669
|
T | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(141): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.2150-45A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976669 | ||||||
chr1:976690
|
C | G | 1 | a0016c0037t0009g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2150-66G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976690 | ||||||
chr1:976706
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2150-82G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976706 | ||||||
chr1:976708
|
A | ACCCCCAC others(25): Show |
2 | a0002c0005t0005g0222a0002c0005t0009g0190 | 2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2150-85_2150-84ins others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976708 | ||||||
chr1:976708
|
A | ACCCCCAC others(118): Show |
1 | a0006c0008t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2150-85_2150-84ins others(125): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976708 | ||||||
chr1:976708
|
A | ACCCCCAC others(681): Show |
1 | a0001c0001t0017g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2150-85_2150-84ins others(688): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976708 | ||||||
chr1:976708
|
A | ACCCCCAC others(618): Show |
1 | a0001c0001t0001g0172 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2150-85_2150-84ins others(625): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976708 | ||||||
chr1:976708
|
A | ACCCCCAC others(683): Show |
1 | a0001c0001t0001g0143 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2150-85_2150-84ins others(690): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976708 | ||||||
chr1:976708
|
A | ACCCCCAC others(681): Show |
1 | a0001c0001t0001g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2150-85_2150-84ins others(688): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976708 | ||||||
chr1:976714
|
A | ACCAACCC others(188): Show |
1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2150-91_2150-90ins others(195): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976714 | ||||||
chr1:976714
|
A | ACCAACCC others(25): Show |
1 | a0005c0006t0004g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2150-122_2150-91du others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976714 | ||||||
chr1:976714
|
A | G | 1 | a0020c0023t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2150-90T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976714 | ||||||
chr1:976714
|
ACCAACCC others(25): Show |
A | 1 | a0002c0005t0008g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2150-122_2150-91de others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976714 | ||||||
chr1:976715
|
C | CCAACCCC others(24): Show |
5 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0122others(2): Show | 7 | HG00438.hp2 HG01070.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-92_2150-91ins others(31): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976715
|
C | CCAACCCC others(681): Show |
1 | a0001c0001t0001g0175 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2150-92_2150-91ins others(688): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976715
|
C | CCAACCCC others(55): Show |
65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(62): Show | 104 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.2150-92_2150-91ins others(62): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976715
|
C | CCAACCCC others(744): Show |
1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2150-92_2150-91ins others(751): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976715
|
C | CCAACCCC others(242): Show |
1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2150-92_2150-91ins others(249): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976715
|
C | CCAACCCC others(743): Show |
3 | a0001c0001t0001g0165a0006c0008t0001g0089a0006c0008t0001g0091 | 3 | HG00639.hp1 HG01106.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2150-92_2150-91ins others(750): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976715
|
C | CCAACCCC others(774): Show |
1 | a0006c0008t0001g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2150-92_2150-91ins others(781): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976715
|
C | CCAACCCC others(743): Show |
1 | a0001c0028t0004g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2150-92_2150-91ins others(750): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976715
|
C | CCAACCCC others(652): Show |
1 | a0001c0001t0001g0167 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2150-92_2150-91ins others(659): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976715
|
CCAACCCC others(279): Show |
C | 1 | a0003c0003t0004g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2150-377_2150-92de others(1): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976715 | ||||||
chr1:976718
|
A | ACCCCAGG others(87): Show |
1 | a0011c0041t0001g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2150-95_2150-94ins others(94): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976718 | ||||||
chr1:976719
|
C | CCCCAGGA others(23): Show |
1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-96_2150-95ins others(30): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976719 | ||||||
chr1:976722
|
C | CAGGAACC others(187): Show |
1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-99_2150-98ins others(194): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976722 | ||||||
chr1:976723
|
G | A | 107 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0104others(104): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2150-99C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976723 | ||||||
chr1:976737
|
A | G | 4 | a0003c0003t0004g0021a0003c0003t0004g0055a0003c0003t0004g0066others(1): Show | 5 | HG01109.hp1 HG02055.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-113T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976737 | ||||||
chr1:976737
|
ACTCCCCC others(279): Show |
A | 1 | a0003c0003t0004g0009 | 5 | HG01516.hp1 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-399_2150-114d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976737 | ||||||
chr1:976737
|
ACTCCCCC others(311): Show |
A | 4 | a0003c0003t0004g0026a0003c0003t0004g0065a0003c0003t0004g0071others(1): Show | 5 | HG00140.hp2 HG00735.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-431_2150-114d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976737 | ||||||
chr1:976745
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-121G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976745 | ||||||
chr1:976745
|
CG | C | 19 | a0001c0001t0001g0041a0001c0001t0001g0123a0001c0001t0001g0124others(16): Show | 27 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.2150-122delC | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976745 | ||||||
chr1:976746
|
G | A | 41 | a0001c0001t0001g0157a0001c0001t0001g0164a0001c0001t0001g0167others(38): Show | 52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.2150-122C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976746 | ||||||
chr1:976746
|
G | C | 2 | a0001c0001t0001g0186a0002c0002t0002g0253 | 2 | HG01978.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.2150-122C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976746 | ||||||
chr1:976746
|
GC | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(151): Show | 260 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.2150-123delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976746 | ||||||
chr1:976747
|
C | A | 20 | a0001c0001t0001g0041a0001c0001t0001g0123a0001c0001t0001g0124others(17): Show | 28 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2150-123G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976747 | ||||||
chr1:976747
|
C | CAACCCCG others(150): Show |
1 | a0001c0001t0013g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2150-124_2150-123i others(159): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976747 | ||||||
chr1:976747
|
C | G | 1 | a0002c0002t0002g0253 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2150-123G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976747 | ||||||
chr1:976747
|
CCAACCCC others(247): Show |
C | 7 | a0003c0003t0004g0015a0003c0003t0004g0023a0003c0003t0004g0051others(4): Show | 10 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.2150-377_2150-124d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976747 | ||||||
chr1:976747
|
CCAACCCC others(342): Show |
C | 6 | a0003c0003t0004g0021a0003c0003t0004g0024a0003c0003t0004g0066others(3): Show | 8 | HG00558.hp2 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.2150-472_2150-124d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976747 | ||||||
chr1:976769
|
A | G | 20 | a0001c0001t0013g0115a0002c0002t0001g0057a0002c0002t0002g0013others(17): Show | 26 | HG01167.hp1 HG01256.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2150-145T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976769 | ||||||
chr1:976772
|
CCCCCCGC others(341): Show |
C | 1 | a0003c0003t0004g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2150-496_2150-149d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976772 | ||||||
chr1:976774
|
C | T | 1 | a0002c0002t0002g0243 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2150-150G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976774 | ||||||
chr1:976778
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(126): Show | 203 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.2150-154C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976778 | ||||||
chr1:976778
|
G | C | 1 | a0008c0012t0002g0202 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2150-154C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976778 | ||||||
chr1:976778
|
GC | G | 84 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0041others(81): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.2150-155delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976778 | ||||||
chr1:976779
|
C | G | 2 | a0001c0001t0003g0109a0008c0012t0002g0202 | 2 | HG02523.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.2150-155G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976779 | ||||||
chr1:976779
|
CCAACCCC others(215): Show |
C | 2 | a0003c0003t0004g0014a0003c0003t0004g0025 | 5 | HG01257.hp1 HG01517.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-377_2150-156d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976779 | ||||||
chr1:976801
|
A | G | 20 | a0001c0001t0013g0115a0002c0002t0001g0057a0002c0002t0002g0013others(17): Show | 23 | HG01167.hp1 HG01256.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.2150-177T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976801 | ||||||
chr1:976809
|
C | A | 1 | a0002c0005t0004g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2150-185G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976809 | ||||||
chr1:976809
|
C | G | 1 | a0006c0008t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2150-185G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976809 | ||||||
chr1:976810
|
G | A | 96 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0122others(93): Show | 166 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.2150-186C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(495): Show |
1 | a0001c0001t0001g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2150-187_2150-186i others(504): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(461): Show |
1 | a0001c0001t0001g0138 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2150-187_2150-186i others(470): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(55): Show |
11 | a0001c0001t0001g0032a0001c0001t0001g0129a0001c0001t0001g0140others(8): Show | 12 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150-187_2150-186i others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(430): Show |
1 | a0001c0001t0001g0173 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2150-187_2150-186i others(439): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(652): Show |
1 | a0001c0001t0001g0142 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2150-187_2150-186i others(661): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(431): Show |
1 | a0001c0034t0001g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2150-187_2150-186i others(440): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(430): Show |
33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0031others(30): Show | 63 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2150-187_2150-186i others(439): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(651): Show |
1 | a0001c0001t0001g0146 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2150-187_2150-186i others(660): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(649): Show |
1 | a0001c0001t0001g0002 | 2 | NA18945.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2150-187_2150-186i others(658): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(680): Show |
2 | a0001c0001t0001g0136a0001c0001t0007g0034 | 2 | HG00597.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2150-187_2150-186i others(689): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(430): Show |
1 | a0001c0001t0001g0137 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2150-187_2150-186i others(439): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
G | GCAACCCC others(461): Show |
1 | a0001c0001t0001g0035 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2150-187_2150-186i others(470): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976810
|
GC | G | 58 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0041others(55): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2150-187delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976810 | ||||||
chr1:976811
|
C | CAAACCCC others(313): Show |
1 | a0001c0001t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2150-188_2150-187i others(322): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976811 | ||||||
chr1:976811
|
C | CAACCCCG others(395): Show |
1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-188_2150-187i others(404): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976811 | ||||||
chr1:976811
|
C | CAACCCCG others(86): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0130a0001c0001t0001g0141 | 3 | HG02129.hp2 HG02132.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2150-188_2150-187i others(95): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976811 | ||||||
chr1:976811
|
C | CAACCCCG others(461): Show |
1 | a0001c0001t0001g0033 | 2 | NA19002.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2150-188_2150-187i others(470): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976811 | ||||||
chr1:976811
|
C | CAACCCCG others(523): Show |
1 | a0001c0001t0001g0134 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2150-188_2150-187i others(532): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976811 | ||||||
chr1:976811
|
CCAACCCC others(183): Show |
C | 5 | a0003c0003t0004g0022a0003c0003t0004g0062a0003c0003t0004g0079others(2): Show | 6 | HG01167.hp1 HG01346.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150-377_2150-188d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976811 | ||||||
chr1:976812
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2150-188G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976812 | ||||||
chr1:976815
|
C | CCCCGGGA others(301): Show |
2 | a0002c0002t0002g0248a0002c0002t0002g0249 | 2 | HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2150-192_2150-191i others(310): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976815 | ||||||
chr1:976825
|
C | T | 1 | a0002c0002t0002g0247 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2150-201G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976825 | ||||||
chr1:976833
|
A | G | 71 | a0001c0001t0002g0008a0001c0001t0002g0105a0001c0001t0002g0106others(68): Show | 137 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.2150-209T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976833 | ||||||
chr1:976836
|
CCCCCCGC others(182): Show |
C | 1 | a0003c0003t0004g0061 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2150-401_2150-213d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976836 | ||||||
chr1:976841
|
C | G | 1 | a0011c0041t0001g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2150-217G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976841 | ||||||
chr1:976842
|
G | A | 115 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0104others(112): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2150-218C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976842 | ||||||
chr1:976842
|
G | C | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2150-218C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976842 | ||||||
chr1:976842
|
G | GCAACCCC others(53): Show |
1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-219_2150-218i others(62): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976842 | ||||||
chr1:976842
|
G | GCAACCCC others(399): Show |
3 | a0001c0001t0001g0037a0001c0001t0001g0098a0001c0001t0001g0177 | 4 | HG00280.hp1 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-219_2150-218i others(408): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976842 | ||||||
chr1:976842
|
GC | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(83): Show | 126 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.2150-219delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976842 | ||||||
chr1:976842
|
GCCAACCC others(58): Show |
G | 1 | a0001c0001t0001g0117 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2150-283_2150-219d others(67): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976842 | ||||||
chr1:976843
|
C | A | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2150-219G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976843 | ||||||
chr1:976843
|
C | CAACCCCG others(618): Show |
1 | a0001c0001t0001g0036 | 2 | HG01255.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2150-220_2150-219i others(627): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976843 | ||||||
chr1:976843
|
C | CAACCCCG others(650): Show |
1 | a0001c0001t0001g0144 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2150-220_2150-219i others(659): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976843 | ||||||
chr1:976843
|
CCAACCCC others(151): Show |
C | 1 | a0003c0003t0004g0078 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2150-377_2150-220d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976843 | ||||||
chr1:976845
|
A | C | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2150-221T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976845 | ||||||
chr1:976865
|
A | G | 70 | a0001c0001t0002g0008a0001c0001t0002g0105a0001c0001t0002g0106others(67): Show | 136 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.2150-241T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976865 | ||||||
chr1:976873
|
C | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0007g0034others(2): Show | 7 | HG02683.hp1 HG02698.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-249G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976873 | ||||||
chr1:976874
|
G | A | 95 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0104others(92): Show | 163 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2150-250C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976874 | ||||||
chr1:976874
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2150-250C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976874 | ||||||
chr1:976874
|
GC | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0031others(106): Show | 164 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.2150-251delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976874 | ||||||
chr1:976874
|
GCCAACCC others(26): Show |
G | 1 | a0001c0015t0002g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2150-283_2150-251d others(35): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976874 | ||||||
chr1:976875
|
C | CAACCCCG others(23): Show |
1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2150-252_2150-251i others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
C | CAACCCCG others(54): Show |
1 | a0004c0004t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2150-252_2150-251i others(63): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
C | CAACCCCG others(118): Show |
1 | a0001c0001t0001g0183 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2150-252_2150-251i others(127): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
C | CAACCCCG others(304): Show |
1 | a0001c0001t0001g0180 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2150-252_2150-251i others(313): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
C | CAACCCCG others(1244): Show |
1 | a0006c0008t0001g0088 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2150-252_2150-251i others(1253): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
C | CAACCCCG others(398): Show |
1 | a0001c0001t0001g0171 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2150-252_2150-251i others(407): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
C | CAACCCCG others(649): Show |
1 | a0001c0001t0001g0266 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2150-252_2150-251i others(658): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
C | CCAACCCC others(280): Show |
1 | a0010c0013t0019g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2150-252_2150-251i others(289): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
C | G | 1 | a0001c0001t0001g0174 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2150-251G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
CCAACCCC others(88): Show |
C | 2 | a0001c0001t0003g0017a0001c0001t0003g0028 | 5 | HG00642.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-346_2150-252d others(97): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976875
|
CCAACCCC others(119): Show |
C | 1 | a0003c0003t0004g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2150-377_2150-252d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976875 | ||||||
chr1:976876
|
C | A | 2 | a0001c0001t0001g0235a0008c0012t0016g0201 | 2 | HG02523.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.2150-252G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976876 | ||||||
chr1:976878
|
A | C | 2 | a0001c0001t0001g0235a0008c0012t0016g0201 | 2 | HG02523.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.2150-254T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976878 | ||||||
chr1:976882
|
C | G | 1 | a0008c0012t0016g0201 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2150-258G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976882 | ||||||
chr1:976897
|
A | G | 46 | a0001c0001t0002g0106a0002c0002t0001g0057a0002c0002t0002g0006others(43): Show | 77 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.2150-273T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976897 | ||||||
chr1:976900
|
C | T | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2150-276G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976900 | ||||||
chr1:976905
|
C | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0122a0001c0015t0002g0043 | 4 | HG00438.hp2 HG02027.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-281G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976905 | ||||||
chr1:976906
|
G | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0033others(81): Show | 121 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.2150-282C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976906 | ||||||
chr1:976906
|
G | C | 4 | a0001c0001t0001g0182a0001c0001t0003g0102a0001c0001t0003g0107others(1): Show | 4 | NA19009.hp1 NA19054.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-282C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976906 | ||||||
chr1:976906
|
G | GCAACCCC others(55): Show |
1 | a0016c0037t0009g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2150-283_2150-282i others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976906 | ||||||
chr1:976906
|
GC | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(112): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.2150-283delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976906 | ||||||
chr1:976906
|
GCCAACCC others(26): Show |
G | 1 | a0005c0006t0005g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2150-315_2150-283d others(35): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976906 | ||||||
chr1:976907
|
C | CAACCCCG others(23): Show |
4 | a0001c0001t0013g0115a0002c0005t0005g0230a0002c0005t0005g0231others(1): Show | 4 | HG02922.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-284_2150-283i others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976907 | ||||||
chr1:976907
|
C | CAACCCCG others(429): Show |
1 | a0018c0033t0001g0187 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2150-284_2150-283i others(438): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976907 | ||||||
chr1:976907
|
C | CAACCCCG others(367): Show |
2 | a0001c0001t0007g0034a0001c0032t0007g0170 | 2 | HG02683.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2150-284_2150-283i others(376): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976907 | ||||||
chr1:976907
|
C | CAACCCCG others(428): Show |
1 | a0001c0001t0001g0156 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2150-284_2150-283i others(437): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976907 | ||||||
chr1:976907
|
C | CAACCCCG others(429): Show |
1 | a0001c0001t0001g0139 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2150-284_2150-283i others(438): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976907 | ||||||
chr1:976907
|
C | G | 4 | a0001c0001t0001g0182a0001c0001t0003g0102a0001c0001t0003g0107others(1): Show | 4 | NA19009.hp1 NA19054.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-283G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976907 | ||||||
chr1:976907
|
CCAACCCC others(87): Show |
C | 1 | a0003c0022t0004g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2150-377_2150-284d others(96): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976907 | ||||||
chr1:976908
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-284G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976908 | ||||||
chr1:976910
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-286T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976910 | ||||||
chr1:976911
|
C | A | 1 | a0001c0001t0003g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2150-287G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976911 | ||||||
chr1:976911
|
C | CCCCGGGA others(237): Show |
1 | a0003c0026t0002g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2150-288_2150-287i others(246): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976911 | ||||||
chr1:976911
|
C | CCCCGGGA others(205): Show |
12 | a0002c0002t0002g0007a0002c0002t0002g0048a0002c0002t0002g0242others(9): Show | 20 | HG01069.hp2 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2150-288_2150-287i others(214): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976911 | ||||||
chr1:976911
|
C | CCCCGGGA others(205): Show |
1 | a0002c0009t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2150-288_2150-287i others(214): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976911 | ||||||
chr1:976914
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-290G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976914 | ||||||
chr1:976929
|
A | G | 59 | a0001c0001t0002g0008a0001c0001t0002g0105a0001c0001t0002g0106others(56): Show | 114 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.2150-305T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976929 | ||||||
chr1:976932
|
C | CCCCCTCC others(4): Show |
1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-309_2150-308i others(13): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976932 | ||||||
chr1:976937
|
C | G | 17 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0123others(14): Show | 25 | HG00099.hp2 HG01074.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.2150-313G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976937 | ||||||
chr1:976938
|
G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(147): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.2150-314C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976938 | ||||||
chr1:976938
|
G | C | 3 | a0001c0001t0001g0122a0001c0001t0001g0235a0003c0003t0001g0259 | 3 | HG01243.hp1 HG02523.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2150-314C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976938 | ||||||
chr1:976938
|
G | GCAACCCC others(24): Show |
1 | a0002c0005t0005g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2150-315_2150-314i others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976938 | ||||||
chr1:976938
|
G | GCAACCCC others(404): Show |
1 | a0013c0040t0005g0234 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2150-315_2150-314i others(413): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976938 | ||||||
chr1:976938
|
G | GCCAACCC others(25): Show |
2 | a0005c0006t0005g0218a0017c0029t0001g0086 | 2 | HG00733.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2150-315_2150-314i others(34): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976938 | ||||||
chr1:976938
|
GC | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0033others(63): Show | 81 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.2150-315delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976938 | ||||||
chr1:976939
|
C | CAACCCCG others(172): Show |
4 | a0002c0002t0001g0057a0002c0002t0002g0013a0002c0002t0002g0056others(1): Show | 6 | HG02809.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150-316_2150-315i others(181): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976939 | ||||||
chr1:976939
|
C | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0235a0003c0003t0001g0259 | 3 | HG01243.hp1 HG02523.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2150-315G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976939 | ||||||
chr1:976939
|
CCAACCCC others(55): Show |
C | 3 | a0003c0003t0004g0063a0003c0003t0004g0069a0003c0036t0021g0074 | 3 | HG02559.hp2 NA19070.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2150-377_2150-316d others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976939 | ||||||
chr1:976940
|
C | CAACCCGG others(188): Show |
1 | a0001c0001t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2150-317_2150-316i others(197): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976940 | ||||||
chr1:976943
|
C | CCCCGGGA others(205): Show |
1 | a0002c0002t0002g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2150-320_2150-319i others(214): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976943 | ||||||
chr1:976943
|
C | CCCCGGGA others(174): Show |
1 | a0002c0002t0002g0256 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2150-320_2150-319i others(183): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976943 | ||||||
chr1:976943
|
C | CCCCGGGA others(173): Show |
13 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0011others(10): Show | 33 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2150-320_2150-319i others(182): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976943 | ||||||
chr1:976943
|
C | CCCCGGGA others(175): Show |
1 | a0002c0002t0002g0241 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2150-320_2150-319i others(184): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976943 | ||||||
chr1:976943
|
C | CCCCGGGA others(203): Show |
1 | a0002c0002t0002g0050 | 2 | HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2150-320_2150-319i others(212): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976943 | ||||||
chr1:976961
|
A | G | 42 | a0001c0001t0002g0008a0001c0001t0002g0105a0001c0001t0002g0106others(39): Show | 75 | HG00423.hp1 HG00609.hp1 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.2150-337T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976961 | ||||||
chr1:976968
|
C | G | 1 | a0002c0009t0002g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2150-344G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976968 | ||||||
chr1:976969
|
C | CA | 42 | a0001c0001t0001g0151a0001c0001t0001g0182a0001c0001t0002g0008others(39): Show | 75 | HG00423.hp1 HG00609.hp1 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.2150-346_2150-345i others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976969 | ||||||
chr1:976970
|
G | C | 42 | a0001c0001t0001g0151a0001c0001t0001g0182a0001c0001t0002g0008others(39): Show | 75 | HG00423.hp1 HG00609.hp1 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.2150-346C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976970 | ||||||
chr1:976970
|
G | GCAACCCC others(57): Show |
2 | a0002c0005t0005g0229a0002c0005t0005g0233 | 2 | HG02615.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2150-347_2150-346i others(66): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976970 | ||||||
chr1:976970
|
G | GCCAACCC others(26): Show |
1 | a0005c0006t0005g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2150-347_2150-346i others(35): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976970 | ||||||
chr1:976985
|
G | A | 2 | a0002c0002t0002g0248a0002c0002t0002g0249 | 2 | HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2150-361C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976985 | ||||||
chr1:976989
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2150-365G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976989 | ||||||
chr1:976992
|
A | ACCGACCA others(104): Show |
1 | a0002c0009t0002g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2150-369_2150-368i others(113): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976992 | ||||||
chr1:976992
|
A | G | 32 | a0001c0001t0002g0105a0001c0001t0003g0030a0001c0001t0003g0107others(29): Show | 34 | HG00733.hp1 HG00741.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.2150-368T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976992 | ||||||
chr1:976992
|
ACTCCCCC others(24): Show |
A | 2 | a0001c0015t0002g0043a0004c0004t0002g0194 | 2 | HG03139.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2150-399_2150-369d others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976992 | ||||||
chr1:976994
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2150-370A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976994 | ||||||
chr1:976997
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2150-373G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976997 | ||||||
chr1:976999
|
C | G | 1 | a0002c0002t0002g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2150-375G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 976999 | ||||||
chr1:977000
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2150-376G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977000 | ||||||
chr1:977000
|
C | CA | 22 | a0001c0001t0001g0041a0001c0001t0001g0122a0001c0001t0001g0123others(19): Show | 24 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.2150-377_2150-376i others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977000 | ||||||
chr1:977001
|
G | C | 25 | a0001c0001t0001g0041a0001c0001t0001g0122a0001c0001t0001g0123others(22): Show | 27 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.2150-377C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977001 | ||||||
chr1:977001
|
G | GCAACCCC others(25): Show |
3 | a0001c0001t0001g0143a0001c0001t0001g0167a0001c0001t0001g0175 | 3 | HG00323.hp2 HG00621.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2150-378_2150-377i others(34): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977001 | ||||||
chr1:977001
|
GCAACCCC others(57): Show |
G | 1 | a0008c0012t0002g0053 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2150-441_2150-378d others(66): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977001 | ||||||
chr1:977005
|
C | T | 1 | a0002c0009t0002g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2150-381G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977005 | ||||||
chr1:977009
|
G | A | 1 | a0003c0003t0004g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2150-385C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977009 | ||||||
chr1:977023
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(190): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2150-399C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977023 | ||||||
chr1:977023
|
G | C | 1 | a0002c0002t0002g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2150-399C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977023 | ||||||
chr1:977025
|
T | A | 1 | a0002c0002t0002g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2150-401A>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977025 | ||||||
chr1:977028
|
C | G | 1 | a0002c0002t0002g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2150-404G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977028 | ||||||
chr1:977029
|
C | A | 1 | a0002c0002t0002g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2150-405G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977029 | ||||||
chr1:977031
|
C | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0117others(1): Show | 4 | HG02976.hp1 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-407G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977031 | ||||||
chr1:977031
|
CA | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0122a0001c0001t0001g0134others(9): Show | 15 | HG02004.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2150-408delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977031 | ||||||
chr1:977032
|
A | AACCCCGG others(79): Show |
1 | a0002c0002t0002g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2150-409_2150-408i others(88): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977032 | ||||||
chr1:977032
|
A | ACCAACCC others(117): Show |
2 | a0002c0002t0002g0048a0002c0009t0002g0260 | 3 | HG02970.hp1 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2150-409_2150-408i others(126): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977032 | ||||||
chr1:977032
|
A | ACCAACCC others(117): Show |
1 | a0002c0002t0002g0244 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2150-409_2150-408i others(126): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977032 | ||||||
chr1:977032
|
A | G | 4 | a0002c0005t0005g0230a0002c0005t0005g0231a0010c0013t0018g0209others(1): Show | 4 | HG02145.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-408T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977032 | ||||||
chr1:977033
|
C | G | 12 | a0001c0001t0001g0018a0001c0001t0001g0122a0001c0001t0001g0134others(9): Show | 15 | HG02004.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2150-409G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977033 | ||||||
chr1:977037
|
C | T | 1 | a0002c0002t0002g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2150-413G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977037 | ||||||
chr1:977053
|
C | T | 1 | a0001c0001t0003g0012 | 4 | NA18952.hp2 NA18981.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-429G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977053 | ||||||
chr1:977055
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(192): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2150-431C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977055 | ||||||
chr1:977058
|
C | CCCCGCGC others(172): Show |
2 | a0002c0002t0002g0254a0021c0024t0002g0239 | 2 | NA18957.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2150-435_2150-434i others(181): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977058 | ||||||
chr1:977063
|
C | G | 1 | a0001c0001t0003g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2150-439G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977063 | ||||||
chr1:977063
|
CA | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0031others(112): Show | 200 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.2150-440delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977063 | ||||||
chr1:977063
|
CACCAACC others(214): Show |
C | 1 | a0009c0014t0002g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2150-660_2150-440d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977063 | ||||||
chr1:977064
|
A | C | 4 | a0001c0001t0001g0157a0002c0002t0002g0254a0014c0039t0002g0265others(1): Show | 4 | HG02055.hp2 NA18957.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-440T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977064 | ||||||
chr1:977064
|
A | G | 12 | a0001c0001t0001g0148a0001c0001t0001g0162a0001c0001t0001g0171others(9): Show | 16 | HG01074.hp2 HG01928.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2150-440T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977064 | ||||||
chr1:977065
|
C | CAACCCCG others(23): Show |
2 | a0001c0007t0001g0005a0001c0007t0001g0092 | 6 | HG01928.hp2 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2150-442_2150-441i others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CAACCCCG others(211): Show |
1 | a0001c0001t0001g0171 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2150-442_2150-441i others(220): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CAACCCCG others(775): Show |
2 | a0001c0001t0001g0162a0006c0008t0001g0087 | 2 | HG01074.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.2150-442_2150-441i others(784): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CAACCCCG others(778): Show |
1 | a0001c0001t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2150-442_2150-441i others(787): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CCAACCCC others(180): Show |
1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-442_2150-441i others(189): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CCAACCCC others(149): Show |
1 | a0001c0001t0001g0159 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2150-442_2150-441i others(158): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CCAACCCC others(148): Show |
5 | a0001c0001t0001g0035a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG02129.hp2 HG02132.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-442_2150-441i others(157): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CCAACCCC others(650): Show |
1 | a0001c0001t0001g0040 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2150-442_2150-441i others(659): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CCAACCCC others(56): Show |
11 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0136others(8): Show | 13 | HG00597.hp1 HG01070.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.2150-442_2150-441i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CCAACCCC others(637): Show |
1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2150-442_2150-441i others(646): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | CCAACCCC others(151): Show |
1 | a0001c0001t0001g0183 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2150-442_2150-441i others(160): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977065
|
C | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0031others(117): Show | 205 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.2150-441G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977065 | ||||||
chr1:977073
|
G | GGGAACCG others(22): Show |
1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-450_2150-449i others(31): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977073 | ||||||
chr1:977080
|
G | A | 16 | a0002c0002t0001g0057a0002c0002t0002g0007a0002c0002t0002g0013others(13): Show | 25 | HG01069.hp2 HG01123.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.2150-456C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977080 | ||||||
chr1:977080
|
G | GCCTCCCA others(24): Show |
10 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0019others(7): Show | 23 | HG00438.hp1 HG01099.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2150-457_2150-456i others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977080 | ||||||
chr1:977084
|
C | CCCACTCC others(25): Show |
1 | a0002c0002t0002g0241 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2150-461_2150-460i others(34): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977084 | ||||||
chr1:977087
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(196): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.2150-463C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977087 | ||||||
chr1:977094
|
C | G | 1 | a0001c0001t0001g0182 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2150-470G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977094 | ||||||
chr1:977095
|
C | CA | 54 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0040others(51): Show | 71 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2150-472_2150-471i others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977095 | ||||||
chr1:977095
|
C | CACCAACC others(186): Show |
1 | a0002c0005t0005g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2150-472_2150-471i others(195): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977095 | ||||||
chr1:977096
|
G | C | 56 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0040others(53): Show | 73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.2150-472C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977096 | ||||||
chr1:977096
|
G | GC | 4 | a0002c0005t0005g0229a0002c0005t0005g0230a0002c0005t0005g0231others(1): Show | 4 | HG02615.hp1 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-473dupG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977096 | ||||||
chr1:977096
|
G | GCAACCCC others(55): Show |
2 | a0002c0002t0002g0248a0002c0002t0002g0249 | 2 | HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2150-473_2150-472i others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977096 | ||||||
chr1:977096
|
G | GCAACCCC others(25): Show |
6 | a0002c0005t0008g0046a0005c0006t0005g0212a0005c0006t0005g0215others(3): Show | 7 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-504_2150-473d others(34): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977096 | ||||||
chr1:977096
|
G | GCAACCCC others(56): Show |
1 | a0005c0006t0005g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2150-473_2150-472i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977096 | ||||||
chr1:977096
|
GCAACCCC others(182): Show |
G | 1 | a0004c0004t0002g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2150-661_2150-473d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977096 | ||||||
chr1:977111
|
G | A | 7 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0020others(4): Show | 9 | HG01257.hp2 HG01993.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.2150-487C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977111 | ||||||
chr1:977118
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(194): Show | 322 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.2150-494C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977118 | ||||||
chr1:977119
|
CT | C | 17 | a0002c0002t0001g0057a0002c0002t0002g0007a0002c0002t0002g0013others(14): Show | 27 | HG01069.hp2 HG01123.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2150-496delA | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977119 | ||||||
chr1:977120
|
T | C | 1 | a0001c0001t0001g0041 | 2 | HG00099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2150-496A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977120 | ||||||
chr1:977120
|
T | TCGAACTT others(5): Show |
1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2150-497_2150-496i others(14): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977120 | ||||||
chr1:977122
|
C | A | 17 | a0002c0002t0001g0057a0002c0002t0002g0007a0002c0002t0002g0013others(14): Show | 27 | HG01069.hp2 HG01123.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2150-498G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977122 | ||||||
chr1:977124
|
C | G | 1 | a0001c0001t0001g0041 | 2 | HG00099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2150-500G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977124 | ||||||
chr1:977126
|
C | G | 22 | a0001c0001t0002g0008a0001c0001t0002g0105a0001c0001t0002g0106others(19): Show | 54 | HG00423.hp1 HG00609.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.2150-502G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977126 | ||||||
chr1:977126
|
CA | C | 33 | a0001c0001t0001g0035a0001c0001t0001g0123a0001c0001t0001g0124others(30): Show | 42 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.2150-503delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977126 | ||||||
chr1:977126
|
CACCAACC others(246): Show |
C | 2 | a0004c0004t0001g0195a0004c0004t0001g0196 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2150-755_2150-503d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977126 | ||||||
chr1:977126
|
CACCAACC others(278): Show |
C | 2 | a0001c0001t0001g0103a0001c0001t0002g0111 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2150-787_2150-503d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977126 | ||||||
chr1:977127
|
A | C | 2 | a0001c0001t0001g0175a0002c0002t0002g0256 | 2 | NA19000.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2150-503T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977127 | ||||||
chr1:977127
|
A | G | 21 | a0002c0002t0001g0057a0002c0002t0002g0007a0002c0002t0002g0013others(18): Show | 31 | HG01069.hp2 HG01123.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.2150-503T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977127 | ||||||
chr1:977128
|
C | CCAACCCG others(146): Show |
1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2150-505_2150-504i others(155): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977128 | ||||||
chr1:977128
|
C | G | 35 | a0001c0001t0001g0035a0001c0001t0001g0123a0001c0001t0001g0124others(32): Show | 44 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.2150-504G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977128 | ||||||
chr1:977131
|
AC | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0141a0001c0001t0001g0145others(4): Show | 8 | HG00423.hp2 HG01069.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2150-508delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977131 | ||||||
chr1:977135
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2150-511G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977135 | ||||||
chr1:977150
|
G | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(191): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.2150-526C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977150 | ||||||
chr1:977151
|
CT | C | 14 | a0002c0002t0001g0057a0002c0002t0002g0007a0002c0002t0002g0013others(11): Show | 23 | HG01069.hp2 HG01123.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2150-528delA | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977151 | ||||||
chr1:977154
|
C | A | 14 | a0002c0002t0001g0057a0002c0002t0002g0007a0002c0002t0002g0013others(11): Show | 23 | HG01069.hp2 HG01123.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2150-530G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977154 | ||||||
chr1:977156
|
C | T | 3 | a0003c0003t0001g0259a0003c0018t0001g0237a0008c0012t0002g0053 | 3 | HG01243.hp1 HG01243.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2150-532G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977156 | ||||||
chr1:977158
|
CA | C | 43 | a0001c0001t0001g0041a0001c0001t0001g0134a0001c0001t0001g0151others(40): Show | 92 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2150-535delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977158 | ||||||
chr1:977158
|
CACCAACC others(118): Show |
C | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2150-659_2150-535d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977158 | ||||||
chr1:977158
|
CACCAACC others(119): Show |
C | 4 | a0001c0001t0003g0112a0001c0001t0003g0121a0001c0001t0014g0116others(1): Show | 4 | HG02280.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-660_2150-535d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977158 | ||||||
chr1:977159
|
A | C | 1 | a0002c0002t0002g0241 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2150-535T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977159 | ||||||
chr1:977159
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0031others(61): Show | 105 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.2150-535T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977159 | ||||||
chr1:977160
|
C | CAACCCCG others(23): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0150a0001c0001t0001g0154others(5): Show | 8 | HG00558.hp1 HG02015.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.2150-537_2150-536i others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CAACCCCG others(54): Show |
38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0031others(35): Show | 69 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.2150-537_2150-536i others(63): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CAACCCCG others(53): Show |
1 | a0001c0001t0001g0133 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2150-537_2150-536i others(62): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCC others(431): Show |
1 | a0001c0001t0001g0141 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2150-537_2150-536i others(440): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCC others(86): Show |
1 | a0002c0002t0002g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2150-537_2150-536i others(95): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCC others(428): Show |
1 | a0001c0001t0001g0145 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2150-537_2150-536i others(437): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCC others(430): Show |
1 | a0006c0008t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2150-537_2150-536i others(439): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCC others(399): Show |
1 | a0001c0030t0001g0096 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2150-537_2150-536i others(408): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCC others(429): Show |
1 | a0001c0001t0010g0147 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2150-537_2150-536i others(438): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCC others(334): Show |
1 | a0001c0001t0001g0032 | 2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.2150-537_2150-536i others(343): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCC others(428): Show |
1 | a0001c0001t0001g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2150-537_2150-536i others(437): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCG others(459): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0140a0001c0001t0001g0174 | 5 | HG02129.hp1 NA18977.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-537_2150-536i others(468): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | CCAACCCG others(490): Show |
1 | a0011c0041t0001g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2150-537_2150-536i others(499): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977160
|
C | G | 44 | a0001c0001t0001g0041a0001c0001t0001g0134a0001c0001t0001g0151others(41): Show | 93 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2150-536G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977160 | ||||||
chr1:977175
|
G | A | 8 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0049others(5): Show | 19 | HG00438.hp1 HG01258.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.2150-551C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977175 | ||||||
chr1:977182
|
G | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(186): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2150-558C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977182 | ||||||
chr1:977186
|
C | A | 1 | a0002c0002t0002g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2150-562G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977186 | ||||||
chr1:977187
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-563G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977187 | ||||||
chr1:977188
|
C | T | 2 | a0001c0001t0013g0115a0001c0015t0002g0043 | 3 | HG02976.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2150-564G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977188 | ||||||
chr1:977190
|
CA | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0040others(50): Show | 104 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2150-567delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977190 | ||||||
chr1:977190
|
CACCAACC others(86): Show |
C | 1 | a0001c0001t0003g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2150-659_2150-567d others(95): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977190 | ||||||
chr1:977190
|
CACCAACC others(87): Show |
C | 10 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0012g0113others(7): Show | 20 | HG00408.hp2 HG00673.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.2150-660_2150-567d others(96): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977190 | ||||||
chr1:977190
|
CACCAACC others(246): Show |
C | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2150-819_2150-567d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977190 | ||||||
chr1:977191
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-567T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977191 | ||||||
chr1:977191
|
A | G | 12 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0011others(9): Show | 16 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.2150-567T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977191 | ||||||
chr1:977192
|
C | CAACCCCG others(23): Show |
5 | a0002c0002t0002g0006a0002c0002t0002g0010a0002c0002t0002g0011others(2): Show | 9 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.2150-569_2150-568i others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977192 | ||||||
chr1:977192
|
C | CAACCCCG others(117): Show |
2 | a0002c0002t0002g0254a0021c0024t0002g0239 | 2 | NA18957.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2150-569_2150-568i others(126): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977192 | ||||||
chr1:977192
|
C | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0040others(51): Show | 105 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.2150-568G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977192 | ||||||
chr1:977194
|
A | AACCCCGG others(150): Show |
1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-571_2150-570i others(159): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977194 | ||||||
chr1:977207
|
G | A | 2 | a0002c0002t0002g0020a0002c0002t0002g0256 | 4 | NA18947.hp2 NA18987.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-583C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977207 | ||||||
chr1:977214
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(173): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.2150-590C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977214 | ||||||
chr1:977215
|
CT | C | 3 | a0002c0005t0004g0224a0002c0005t0005g0228a0002c0009t0002g0261 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2150-592delA | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977215 | ||||||
chr1:977218
|
C | A | 3 | a0002c0005t0004g0224a0002c0005t0005g0228a0002c0009t0002g0261 | 3 | HG02622.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2150-594G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977218 | ||||||
chr1:977220
|
CCCACCAA others(53): Show |
C | 1 | a0003c0003t0004g0061 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2150-656_2150-597d others(62): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977220 | ||||||
chr1:977222
|
C | G | 2 | a0001c0001t0003g0017a0001c0001t0003g0028 | 5 | HG00642.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-598G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977222 | ||||||
chr1:977222
|
CA | C | 43 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(40): Show | 74 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2150-599delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977222 | ||||||
chr1:977222
|
CACCAACC others(54): Show |
C | 2 | a0001c0001t0001g0179a0003c0036t0021g0074 | 2 | NA18957.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2150-659_2150-599d others(63): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977222 | ||||||
chr1:977222
|
CACCAACC others(55): Show |
C | 2 | a0004c0004t0002g0191a0004c0004t0002g0194 | 2 | NA19081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2150-660_2150-599d others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977222 | ||||||
chr1:977223
|
A | C | 3 | a0001c0001t0001g0183a0002c0002t0002g0253a0002c0002t0002g0256 | 3 | HG01978.hp1 NA18947.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2150-599T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977223 | ||||||
chr1:977223
|
A | G | 8 | a0002c0005t0004g0224a0002c0005t0005g0228a0002c0005t0005g0229others(5): Show | 8 | HG00280.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2150-599T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977223 | ||||||
chr1:977224
|
C | CAACCCCG others(400): Show |
1 | a0006c0008t0001g0088 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2150-601_2150-600i others(409): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977224 | ||||||
chr1:977224
|
C | CCAACCCG others(272): Show |
1 | a0001c0001t0001g0162 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2150-601_2150-600i others(281): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977224 | ||||||
chr1:977224
|
C | G | 46 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0041others(43): Show | 77 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2150-600G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977224 | ||||||
chr1:977224
|
CCAACCCC others(85): Show |
C | 32 | a0003c0003t0004g0009a0003c0003t0004g0014a0003c0003t0004g0015others(29): Show | 46 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.2150-692_2150-601d others(94): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977224 | ||||||
chr1:977227
|
AC | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0040others(23): Show | 33 | HG00597.hp1 HG01070.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.2150-604delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977227 | ||||||
chr1:977227
|
ACCCCGGG others(310): Show |
A | 1 | a0001c0001t0001g0182 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2150-920_2150-604d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977227 | ||||||
chr1:977243
|
C | G | 2 | a0002c0005t0004g0224a0002c0005t0005g0228 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2150-619G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977243 | ||||||
chr1:977246
|
A | C | 2 | a0002c0005t0004g0224a0002c0005t0005g0228 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2150-622T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977246 | ||||||
chr1:977246
|
A | G | 12 | a0001c0001t0013g0115a0002c0005t0005g0222a0002c0005t0005g0229others(9): Show | 12 | HG00733.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150-622T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977246 | ||||||
chr1:977246
|
ACCACCCC others(22): Show |
A | 17 | a0001c0001t0001g0151a0001c0001t0002g0008a0001c0001t0002g0105others(14): Show | 49 | HG00423.hp1 HG00609.hp1 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.2150-651_2150-623d others(31): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977246 | ||||||
chr1:977247
|
C | CT | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(107): Show | 158 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.2150-624_2150-623i others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977247 | ||||||
chr1:977247
|
C | CTCCCCCC others(25): Show |
7 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0001g0165others(4): Show | 9 | HG00099.hp1 HG00621.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.2150-624_2150-623i others(34): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977247 | ||||||
chr1:977247
|
C | CTCCCCCC others(273): Show |
5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0028t0004g0080others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-624_2150-623i others(282): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977247 | ||||||
chr1:977247
|
C | CTCCCCCC others(1025): Show |
1 | a0001c0001t0001g0124 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2150-624_2150-623i others(1034): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977247 | ||||||
chr1:977247
|
C | CTCCCCCC others(25): Show |
3 | a0002c0002t0002g0048a0002c0002t0002g0244a0002c0009t0002g0260 | 4 | HG02109.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-624_2150-623i others(34): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977247 | ||||||
chr1:977247
|
C | CTCCCCCC others(278): Show |
1 | a0002c0005t0005g0233 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2150-624_2150-623i others(287): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977247 | ||||||
chr1:977248
|
C | T | 9 | a0001c0001t0001g0178a0001c0001t0001g0235a0001c0001t0007g0034others(6): Show | 11 | HG02523.hp2 HG02683.hp1 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.2150-624G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977248 | ||||||
chr1:977249
|
A | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(132): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2150-625T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977249 | ||||||
chr1:977253
|
C | G | 2 | a0002c0005t0004g0224a0002c0005t0005g0228 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2150-629G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977253 | ||||||
chr1:977254
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(115): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.2150-630C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977254 | ||||||
chr1:977254
|
G | C | 6 | a0001c0001t0001g0178a0001c0001t0007g0034a0001c0032t0007g0170others(3): Show | 8 | HG02683.hp1 HG03704.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.2150-630C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977254 | ||||||
chr1:977254
|
GCCAACCC others(24): Show |
G | 2 | a0001c0001t0003g0017a0001c0001t0003g0028 | 5 | HG00642.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-661_2150-631d others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977254 | ||||||
chr1:977255
|
C | G | 6 | a0001c0001t0001g0178a0001c0001t0007g0034a0001c0032t0007g0170others(3): Show | 8 | HG02683.hp1 HG03704.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.2150-631G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977255 | ||||||
chr1:977263
|
G | A | 1 | a0002c0009t0002g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2150-639C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977263 | ||||||
chr1:977265
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-641C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977265 | ||||||
chr1:977269
|
CGCCTGCC others(583): Show |
C | 1 | a0001c0001t0001g0041 | 2 | HG00099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2149+1022_2150-646 others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977269 | ||||||
chr1:977270
|
G | A | 1 | a0002c0002t0002g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2150-646C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977270 | ||||||
chr1:977273
|
T | TCCC | 3 | a0002c0005t0005g0230a0002c0005t0005g0231a0002c0005t0005g0233 | 3 | HG02615.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-650_2150-649i others(5): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977273 | ||||||
chr1:977273
|
T | TCCCGCTC others(216): Show |
1 | a0002c0005t0005g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2150-650_2150-649i others(225): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977273 | ||||||
chr1:977274
|
G | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(130): Show | 200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.2150-650C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977274 | ||||||
chr1:977275
|
C | CCA | 38 | a0001c0001t0001g0003a0001c0001t0001g0124a0001c0001t0001g0162others(35): Show | 65 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2150-652_2150-651i others(4): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977275 | ||||||
chr1:977275
|
C | CCACTCCC others(59): Show |
2 | a0002c0011t0002g0047a0002c0011t0002g0238 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2150-652_2150-651i others(68): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977275 | ||||||
chr1:977275
|
C | CCG | 5 | a0002c0005t0005g0222a0002c0005t0009g0190a0010c0013t0018g0209others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-652_2150-651i others(4): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977275 | ||||||
chr1:977276
|
C | CACT | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(79): Show | 118 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2150-653_2150-652i others(5): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977276 | ||||||
chr1:977276
|
C | CGCTCCCC others(207): Show |
1 | a0017c0029t0001g0086 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2150-653_2150-652i others(216): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977276 | ||||||
chr1:977276
|
C | T | 4 | a0002c0005t0005g0229a0002c0005t0005g0230a0002c0005t0005g0231others(1): Show | 4 | HG02615.hp1 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-652G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977276 | ||||||
chr1:977277
|
C | A | 5 | a0002c0002t0002g0020a0002c0002t0002g0254a0002c0002t0002g0256others(2): Show | 7 | NA18947.hp2 NA18957.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.2150-653G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977277 | ||||||
chr1:977277
|
C | CCCGCCAC others(243): Show |
1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2150-654_2150-653i others(252): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977277 | ||||||
chr1:977277
|
C | T | 62 | a0001c0001t0001g0003a0001c0001t0001g0124a0001c0001t0001g0151others(59): Show | 122 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.2150-653G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977277 | ||||||
chr1:977280
|
A | AC | 5 | a0002c0002t0002g0020a0002c0002t0002g0254a0002c0002t0002g0256others(2): Show | 7 | NA18947.hp2 NA18957.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.2150-657dupG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977280 | ||||||
chr1:977280
|
A | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(146): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2150-656T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977280 | ||||||
chr1:977280
|
A | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0040others(26): Show | 39 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.2150-656T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977280 | ||||||
chr1:977282
|
CG | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0040others(26): Show | 39 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.2150-659delC | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977282 | ||||||
chr1:977283
|
G | A | 2 | a0001c0001t0001g0099a0006c0008t0001g0087 | 2 | HG03490.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2150-659C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977283 | ||||||
chr1:977283
|
G | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0124a0001c0001t0001g0151others(67): Show | 132 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.2150-659C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977283 | ||||||
chr1:977283
|
GA | G | 8 | a0001c0028t0004g0080a0002c0002t0002g0048a0002c0002t0002g0244others(5): Show | 9 | HG00738.hp2 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2150-660delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977283 | ||||||
chr1:977283
|
GAC | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(74): Show | 112 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2150-661_2150-660d others(4): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977283 | ||||||
chr1:977284
|
A | G | 5 | a0002c0002t0002g0020a0002c0002t0002g0254a0002c0002t0002g0256others(2): Show | 7 | NA18947.hp2 NA18957.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.2150-660T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977284 | ||||||
chr1:977285
|
C | CCCCGGGA others(149): Show |
1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2150-662_2150-661i others(158): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977285 | ||||||
chr1:977285
|
C | CCCCGGGA others(80): Show |
1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-662_2150-661i others(89): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977285 | ||||||
chr1:977285
|
C | CCCCGGGA others(145): Show |
1 | a0006c0008t0001g0087 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2150-662_2150-661i others(154): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977285 | ||||||
chr1:977285
|
C | G | 17 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0003g0112others(14): Show | 27 | HG00408.hp2 HG00673.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.2150-661G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977285 | ||||||
chr1:977295
|
G | GAACCGCC others(190): Show |
1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-672_2150-671i others(199): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977295 | ||||||
chr1:977307
|
A | G | 13 | a0002c0005t0004g0224a0002c0005t0005g0222a0002c0005t0005g0228others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2150-683T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977307 | ||||||
chr1:977309
|
T | TCCCCCCG others(401): Show |
1 | a0001c0001t0001g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2150-686_2150-685i others(410): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977309 | ||||||
chr1:977315
|
C | CA | 39 | a0001c0001t0001g0178a0002c0002t0001g0057a0002c0002t0002g0006others(36): Show | 68 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.2150-692_2150-691i others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977315 | ||||||
chr1:977316
|
G | A | 2 | a0001c0001t0001g0179a0002c0002t0002g0241 | 2 | NA18957.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2150-692C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977316 | ||||||
chr1:977316
|
G | C | 40 | a0001c0001t0001g0178a0001c0001t0003g0107a0002c0002t0001g0057others(37): Show | 69 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.2150-692C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977316 | ||||||
chr1:977316
|
G | GC | 3 | a0002c0005t0005g0230a0002c0005t0005g0231a0002c0005t0005g0233 | 3 | HG02615.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-693dupG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977316 | ||||||
chr1:977316
|
G | GCAACCCC others(181): Show |
4 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0017g0208others(1): Show | 4 | HG00099.hp1 HG01106.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-693_2150-692i others(190): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977316 | ||||||
chr1:977316
|
G | GCAACCCC others(25): Show |
6 | a0002c0005t0005g0045a0002c0005t0005g0225a0002c0005t0005g0226others(3): Show | 7 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2150-724_2150-693d others(34): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977316 | ||||||
chr1:977318
|
A | C | 2 | a0001c0001t0001g0179a0002c0002t0002g0241 | 2 | NA18957.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2150-694T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977318 | ||||||
chr1:977320
|
C | A | 2 | a0001c0001t0001g0179a0002c0002t0002g0241 | 2 | NA18957.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2150-696G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977320 | ||||||
chr1:977322
|
C | G | 1 | a0001c0001t0003g0102 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2150-698G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977322 | ||||||
chr1:977338
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(190): Show | 318 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.2150-714C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977338 | ||||||
chr1:977342
|
C | A | 2 | a0002c0002t0002g0245a0017c0029t0001g0086 | 2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2150-718G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977342 | ||||||
chr1:977342
|
CCCCCACC others(491): Show |
C | 2 | a0003c0003t0001g0259a0003c0018t0001g0237 | 2 | HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2149+1041_2150-719 others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977342 | ||||||
chr1:977346
|
CA | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0036others(20): Show | 34 | HG00597.hp1 HG00621.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.2150-723delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977346 | ||||||
chr1:977347
|
A | G | 14 | a0001c0001t0001g0125a0001c0001t0001g0168a0001c0001t0001g0172others(11): Show | 15 | HG00733.hp1 HG01074.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.2150-723T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977347 | ||||||
chr1:977348
|
C | CAACCCCG others(86): Show |
1 | a0001c0001t0001g0172 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2150-725_2150-724i others(95): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977348 | ||||||
chr1:977348
|
C | CAACCCCG others(464): Show |
1 | a0001c0001t0001g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2150-725_2150-724i others(473): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977348 | ||||||
chr1:977348
|
C | CAACCCCG others(494): Show |
1 | a0001c0001t0001g0168 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2150-725_2150-724i others(503): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977348 | ||||||
chr1:977348
|
C | CCAACCCC others(86): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0159 | 2 | NA18944.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.2150-725_2150-724i others(95): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977348 | ||||||
chr1:977348
|
C | CCAACCCC others(244): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0184 | 3 | HG00438.hp2 HG02129.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2150-725_2150-724i others(253): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977348 | ||||||
chr1:977348
|
C | CCAACCCC others(310): Show |
1 | a0002c0005t0005g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2150-725_2150-724i others(319): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977348 | ||||||
chr1:977348
|
C | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0036others(20): Show | 34 | HG00597.hp1 HG00621.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.2150-724G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977348 | ||||||
chr1:977363
|
G | T | 1 | a0002c0002t0002g0248 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2150-739C>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977363 | ||||||
chr1:977370
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(170): Show | 267 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2150-746C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977370 | ||||||
chr1:977372
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2150-748A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977372 | ||||||
chr1:977374
|
CCCCCACC others(459): Show |
C | 1 | a0001c0015t0002g0043 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2149+1041_2150-751 others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977374 | ||||||
chr1:977376
|
C | G | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2150-752G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977376 | ||||||
chr1:977376
|
C | T | 13 | a0001c0001t0001g0114a0001c0001t0003g0120a0001c0001t0012g0113others(10): Show | 23 | HG00408.hp2 HG00673.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.2150-752G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977376 | ||||||
chr1:977378
|
CA | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0040others(42): Show | 81 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.2150-755delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977378 | ||||||
chr1:977378
|
CACCAACC others(430): Show |
C | 1 | a0008c0012t0002g0053 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2149+1066_2150-755 others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977378 | ||||||
chr1:977379
|
A | G | 5 | a0001c0001t0001g0130a0001c0001t0001g0183a0002c0005t0005g0230others(2): Show | 5 | HG02132.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-755T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977379 | ||||||
chr1:977380
|
C | CAACCCCG others(215): Show |
1 | a0001c0001t0001g0183 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2150-757_2150-756i others(224): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977380 | ||||||
chr1:977380
|
C | CAACCCCG others(54): Show |
1 | a0001c0001t0001g0130 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2150-757_2150-756i others(63): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977380 | ||||||
chr1:977380
|
C | G | 47 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0040others(44): Show | 83 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.2150-756G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977380 | ||||||
chr1:977383
|
AC | A | 16 | a0001c0001t0002g0008a0001c0001t0002g0105a0001c0001t0002g0106others(13): Show | 47 | HG00423.hp1 HG00609.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.2150-760delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977383 | ||||||
chr1:977402
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(172): Show | 268 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.2150-778C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977402 | ||||||
chr1:977404
|
T | TCCCCCCG others(93): Show |
1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-781_2150-780i others(102): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977404 | ||||||
chr1:977406
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2150-782G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977406 | ||||||
chr1:977408
|
C | CCCGCAAC others(84): Show |
1 | a0001c0001t0001g0178 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2150-785_2150-784i others(93): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977408 | ||||||
chr1:977408
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0003g0029 | 3 | HG02976.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2150-784G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977408 | ||||||
chr1:977410
|
CA | C | 19 | a0001c0001t0001g0099a0001c0001t0001g0179a0001c0001t0003g0017others(16): Show | 23 | HG00642.hp2 HG00733.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.2150-787delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977410 | ||||||
chr1:977411
|
A | ACCAACCC others(56): Show |
1 | a0002c0009t0002g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2150-788_2150-787i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977411 | ||||||
chr1:977411
|
A | C | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-787T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977411 | ||||||
chr1:977411
|
A | G | 28 | a0001c0001t0001g0123a0002c0002t0002g0006a0002c0002t0002g0007others(25): Show | 55 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.2150-787T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977411 | ||||||
chr1:977412
|
C | CCAACCCC others(117): Show |
1 | a0004c0004t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2150-789_2150-788i others(126): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977412 | ||||||
chr1:977412
|
C | CCAACCCC others(86): Show |
1 | a0001c0001t0001g0178 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2150-789_2150-788i others(95): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977412 | ||||||
chr1:977412
|
C | G | 21 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0179others(18): Show | 25 | HG00642.hp2 HG00733.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.2150-788G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977412 | ||||||
chr1:977414
|
A | G | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-790T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977414 | ||||||
chr1:977415
|
A | C | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-791T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977415 | ||||||
chr1:977416
|
C | CCCCGGGA others(52): Show |
1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-793_2150-792i others(61): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977416 | ||||||
chr1:977420
|
G | C | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-796C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977420 | ||||||
chr1:977434
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(187): Show | 314 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2150-810C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977434 | ||||||
chr1:977438
|
C | A | 2 | a0001c0001t0001g0123a0017c0029t0001g0086 | 2 | HG00733.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2150-814G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977438 | ||||||
chr1:977440
|
C | T | 2 | a0004c0004t0001g0195a0004c0004t0001g0196 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2150-816G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977440 | ||||||
chr1:977442
|
CA | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0040others(52): Show | 100 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.2150-819delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977442 | ||||||
chr1:977443
|
A | ACCAACCC others(56): Show |
1 | a0002c0002t0002g0245 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2150-820_2150-819i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977443 | ||||||
chr1:977443
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-819T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977443 | ||||||
chr1:977443
|
A | G | 26 | a0001c0001t0001g0123a0001c0001t0001g0175a0001c0001t0003g0185others(23): Show | 39 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.2150-819T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977443 | ||||||
chr1:977444
|
C | CAACCCCG others(23): Show |
1 | a0001c0001t0001g0175 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2150-821_2150-820i others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | CAACCCCG others(23): Show |
1 | a0006c0008t0001g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2150-821_2150-820i others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | CCAACCCC others(55): Show |
1 | a0001c0001t0001g0159 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2150-821_2150-820i others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | CCAACCCC others(215): Show |
1 | a0020c0023t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2150-821_2150-820i others(224): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | CCAACCCC others(178): Show |
1 | a0001c0001t0001g0132 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2150-821_2150-820i others(187): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | CCAACCCG others(240): Show |
1 | a0007c0010t0001g0095 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2150-821_2150-820i others(249): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | CCAACCCG others(394): Show |
1 | a0001c0001t0001g0131 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2150-821_2150-820i others(403): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | CCAACCCG others(497): Show |
1 | a0006c0008t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2150-821_2150-820i others(506): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | CCAACCCG others(211): Show |
1 | a0001c0001t0001g0174 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2150-821_2150-820i others(220): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | CCAACCCG others(210): Show |
1 | a0001c0030t0001g0096 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2150-821_2150-820i others(219): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977444
|
C | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0040others(54): Show | 102 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.2150-820G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977444 | ||||||
chr1:977446
|
A | C | 1 | a0001c0001t0003g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2150-822T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977446 | ||||||
chr1:977447
|
AC | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(59): Show | 105 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.2150-824delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977447 | ||||||
chr1:977448
|
C | A | 1 | a0001c0001t0003g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2150-824G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977448 | ||||||
chr1:977466
|
G | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(184): Show | 305 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.2150-842C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977466 | ||||||
chr1:977470
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2150-846G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977470 | ||||||
chr1:977470
|
C | CCCCCGCA others(358): Show |
1 | a0002c0005t0009g0190 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2150-847_2150-846i others(367): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977470 | ||||||
chr1:977472
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0002g0111 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2150-848G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977472 | ||||||
chr1:977473
|
C | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0151a0001c0001t0001g0162others(5): Show | 8 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.2150-849G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977473 | ||||||
chr1:977474
|
CA | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0040others(40): Show | 60 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.2150-851delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977474 | ||||||
chr1:977475
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2150-851T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977475 | ||||||
chr1:977475
|
A | G | 32 | a0001c0001t0001g0123a0002c0002t0001g0057a0002c0002t0002g0006others(29): Show | 56 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2150-851T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977475 | ||||||
chr1:977476
|
C | CAACCCCG others(421): Show |
1 | a0002c0005t0005g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2150-853_2150-852i others(430): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(208): Show |
1 | a0018c0033t0001g0187 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2150-853_2150-852i others(217): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(56): Show |
1 | a0006c0008t0001g0088 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2150-853_2150-852i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(212): Show |
1 | a0001c0001t0001g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2150-853_2150-852i others(221): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(87): Show |
1 | a0006c0008t0001g0087 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2150-853_2150-852i others(96): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(240): Show |
1 | a0001c0001t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2150-853_2150-852i others(249): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(55): Show |
4 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0017g0208others(1): Show | 4 | HG00099.hp1 HG01106.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-853_2150-852i others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(56): Show |
3 | a0002c0002t0002g0048a0002c0002t0002g0244a0002c0009t0002g0260 | 4 | HG02109.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-853_2150-852i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(210): Show |
1 | a0001c0001t0001g0153 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2150-853_2150-852i others(219): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(178): Show |
4 | a0001c0001t0001g0100a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG00673.hp1 HG02040.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-853_2150-852i others(187): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(241): Show |
1 | a0001c0001t0001g0156 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2150-853_2150-852i others(250): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(210): Show |
2 | a0001c0001t0001g0127a0001c0001t0001g0176 | 2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.2150-853_2150-852i others(219): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(209): Show |
36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(33): Show | 68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.2150-853_2150-852i others(218): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(304): Show |
1 | a0001c0001t0001g0128 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2150-853_2150-852i others(313): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(209): Show |
1 | a0001c0034t0001g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2150-853_2150-852i others(218): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(209): Show |
1 | a0001c0001t0001g0031 | 2 | HG02735.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2150-853_2150-852i others(218): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCC others(208): Show |
1 | a0011c0041t0001g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2150-853_2150-852i others(217): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCG others(240): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0038others(5): Show | 9 | HG00438.hp2 HG02015.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.2150-853_2150-852i others(249): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | CCAACCCG others(271): Show |
1 | a0001c0001t0001g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2150-853_2150-852i others(280): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977476
|
C | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0040others(40): Show | 60 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.2150-852G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977476 | ||||||
chr1:977494
|
TCCC | T | 12 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0003g0120others(9): Show | 21 | HG00408.hp2 HG00673.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.2150-873_2150-871d others(5): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977494 | ||||||
chr1:977494
|
TCCCGCTC others(92): Show |
T | 1 | a0004c0004t0002g0042 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2150-969_2150-871d others(101): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977494 | ||||||
chr1:977498
|
G | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(164): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.2150-874C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977498 | ||||||
chr1:977500
|
T | C | 12 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0003g0120others(9): Show | 21 | HG00408.hp2 HG00673.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.2150-876A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977500 | ||||||
chr1:977501
|
C | CCCCCCGC others(21): Show |
2 | a0002c0011t0002g0047a0002c0011t0002g0238 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2150-878_2150-877i others(30): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977501 | ||||||
chr1:977502
|
C | A | 2 | a0001c0001t0001g0123a0002c0005t0005g0222 | 2 | HG04199.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2150-878G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977502 | ||||||
chr1:977504
|
C | G | 12 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0003g0120others(9): Show | 21 | HG00408.hp2 HG00673.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.2150-880G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977504 | ||||||
chr1:977504
|
C | T | 7 | a0001c0001t0003g0017a0001c0001t0003g0028a0001c0001t0003g0112others(4): Show | 10 | HG00642.hp2 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2150-880G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977504 | ||||||
chr1:977506
|
CA | C | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG00733.hp1 HG02132.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2150-883delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977506 | ||||||
chr1:977507
|
A | ACCAACCC others(56): Show |
1 | a0002c0002t0002g0249 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2150-884_2150-883i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977507 | ||||||
chr1:977507
|
A | G | 40 | a0001c0001t0001g0123a0002c0002t0001g0057a0002c0002t0002g0006others(37): Show | 70 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.2150-883T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977507 | ||||||
chr1:977508
|
C | CCAACCCC others(24): Show |
2 | a0002c0011t0002g0047a0002c0011t0002g0238 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2150-885_2150-884i others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977508 | ||||||
chr1:977508
|
C | CCAACCCG others(146): Show |
1 | a0001c0001t0001g0183 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2150-885_2150-884i others(155): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977508 | ||||||
chr1:977508
|
C | G | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(4): Show | 7 | HG02132.hp2 HG02886.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-884G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977508 | ||||||
chr1:977508
|
C | GCAACCCC others(24): Show |
1 | a0017c0029t0001g0086 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2150-884_2150-883i others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977508 | ||||||
chr1:977526
|
TCCC | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0003g0029 | 4 | HG02976.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-905_2150-903d others(5): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977526 | ||||||
chr1:977530
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(190): Show | 315 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2150-906C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977530 | ||||||
chr1:977532
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0003g0029 | 4 | HG02976.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-908A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977532 | ||||||
chr1:977535
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2150-911G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977535 | ||||||
chr1:977536
|
C | CCCACCAA others(52): Show |
1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-913_2150-912i others(61): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977536 | ||||||
chr1:977536
|
C | G | 2 | a0001c0001t0001g0104a0001c0001t0003g0029 | 3 | HG02976.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2150-912G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977536 | ||||||
chr1:977536
|
C | T | 18 | a0001c0001t0002g0008a0001c0001t0002g0105a0001c0001t0002g0106others(15): Show | 49 | HG00423.hp1 HG00609.hp1 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.2150-912G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977536 | ||||||
chr1:977538
|
CA | C | 18 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0001g0130others(15): Show | 27 | HG00408.hp2 HG00673.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.2150-915delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977538 | ||||||
chr1:977539
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2150-915T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977539 | ||||||
chr1:977539
|
A | G | 41 | a0001c0007t0001g0005a0002c0002t0001g0057a0002c0002t0002g0006others(38): Show | 79 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.2150-915T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977539 | ||||||
chr1:977540
|
C | CAACCCCG others(117): Show |
1 | a0001c0007t0001g0005 | 8 | HG01167.hp2 HG01169.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2150-917_2150-916i others(126): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977540 | ||||||
chr1:977540
|
C | G | 18 | a0001c0001t0001g0099a0001c0001t0001g0114a0001c0001t0001g0117others(15): Show | 27 | HG00408.hp2 HG00673.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.2150-916G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977540 | ||||||
chr1:977540
|
C | GCAACCCC others(56): Show |
1 | a0002c0005t0009g0190 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2150-916_2150-915i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977540 | ||||||
chr1:977543
|
AC | A | 4 | a0001c0001t0001g0103a0001c0001t0002g0111a0004c0004t0001g0195others(1): Show | 4 | HG02451.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-920delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977543 | ||||||
chr1:977544
|
C | CCCCGGGA others(428): Show |
1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2150-921_2150-920i others(437): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977544 | ||||||
chr1:977548
|
GGGAACCG others(447): Show |
G | 1 | a0001c0001t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2149+879_2150-925d others(2): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977548 | ||||||
chr1:977555
|
G | GCCTCCCA others(55): Show |
1 | a0001c0001t0001g0172 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2150-932_2150-931i others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977555 | ||||||
chr1:977555
|
G | GCCTCCCA others(24): Show |
1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2150-932_2150-931i others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977555 | ||||||
chr1:977562
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(187): Show | 310 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.2150-938C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977562 | ||||||
chr1:977562
|
G | GCTCCCCC others(453): Show |
1 | a0005c0006t0005g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2150-939_2150-938i others(462): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977562 | ||||||
chr1:977564
|
T | C | 1 | a0004c0004t0002g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2150-940A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977564 | ||||||
chr1:977568
|
C | G | 1 | a0004c0004t0002g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2150-944G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977568 | ||||||
chr1:977570
|
CA | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(117): Show | 205 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.2150-947delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977570 | ||||||
chr1:977571
|
A | ACCAACCC others(56): Show |
1 | a0002c0005t0005g0230 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2150-948_2150-947i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977571 | ||||||
chr1:977571
|
A | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG00558.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2150-947T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977571 | ||||||
chr1:977571
|
A | G | 14 | a0001c0007t0001g0092a0002c0002t0001g0057a0002c0002t0002g0013others(11): Show | 17 | HG02145.hp2 HG02735.hp2 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.2150-947T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977571 | ||||||
chr1:977572
|
C | CAACCCCG others(87): Show |
1 | a0002c0002t0002g0248 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2150-949_2150-948i others(96): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977572 | ||||||
chr1:977572
|
C | CAACCCCG others(484): Show |
1 | a0005c0006t0005g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2150-949_2150-948i others(493): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977572 | ||||||
chr1:977572
|
C | CCAACCCC others(400): Show |
1 | a0001c0001t0001g0159 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2150-949_2150-948i others(409): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977572 | ||||||
chr1:977572
|
C | CCAACCCC others(367): Show |
2 | a0001c0001t0007g0034a0001c0032t0007g0170 | 2 | HG02683.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2150-949_2150-948i others(376): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977572 | ||||||
chr1:977572
|
C | CCAACCCC others(368): Show |
1 | a0001c0001t0001g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2150-949_2150-948i others(377): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977572 | ||||||
chr1:977572
|
C | CCAACCCC others(24): Show |
7 | a0001c0001t0001g0158a0002c0002t0001g0057a0002c0002t0002g0013others(4): Show | 8 | HG02809.hp1 HG02895.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2150-949_2150-948i others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977572 | ||||||
chr1:977572
|
C | CCAACCCC others(56): Show |
1 | a0002c0002t0002g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2150-949_2150-948i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977572 | ||||||
chr1:977572
|
C | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(119): Show | 207 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.2150-948G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977572 | ||||||
chr1:977575
|
AC | A | 8 | a0001c0001t0001g0182a0001c0001t0003g0017a0001c0001t0003g0028others(5): Show | 11 | HG00642.hp2 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150-952delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977575 | ||||||
chr1:977582
|
G | A | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2150-958C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977582 | ||||||
chr1:977583
|
A | G | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2150-959T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977583 | ||||||
chr1:977585
|
C | T | 1 | a0003c0003t0004g0068 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2150-961G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977585 | ||||||
chr1:977590
|
TCCC | T | 5 | a0001c0001t0001g0103a0001c0001t0002g0111a0004c0004t0001g0195others(2): Show | 5 | HG02451.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-969_2150-967d others(5): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977590 | ||||||
chr1:977594
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(174): Show | 269 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.2150-970C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977594 | ||||||
chr1:977596
|
T | C | 6 | a0001c0001t0001g0103a0001c0001t0002g0111a0004c0004t0001g0195others(3): Show | 6 | HG02451.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2150-972A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977596 | ||||||
chr1:977598
|
CCCCCACC others(235): Show |
C | 7 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0012g0113others(4): Show | 11 | HG00673.hp2 HG02155.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.2149+1041_2150-975 others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977598 | ||||||
chr1:977600
|
C | G | 6 | a0001c0001t0001g0103a0001c0001t0002g0111a0004c0004t0001g0195others(3): Show | 6 | HG02451.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2150-976G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977600 | ||||||
chr1:977602
|
CA | C | 12 | a0001c0001t0001g0104a0001c0001t0001g0178a0001c0001t0001g0183others(9): Show | 13 | HG01099.hp2 HG02559.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.2150-979delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977602 | ||||||
chr1:977602
|
CACCAACC others(119): Show |
C | 1 | a0004c0004t0002g0042 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2150-1104_2150-979 others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977602 | ||||||
chr1:977602
|
CACCAACC others(206): Show |
C | 3 | a0004c0004t0002g0004a0004c0004t0002g0194a0009c0014t0002g0200 | 7 | HG01358.hp2 HG01943.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.2149+1066_2150-979 others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977602 | ||||||
chr1:977603
|
A | G | 41 | a0001c0001t0013g0115a0002c0002t0001g0057a0002c0002t0002g0006others(38): Show | 71 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.2150-979T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977603 | ||||||
chr1:977604
|
C | CAACCCCG others(117): Show |
1 | a0001c0001t0013g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2150-981_2150-980i others(126): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977604 | ||||||
chr1:977604
|
C | CCAACCCG others(240): Show |
1 | a0023c0017t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2150-981_2150-980i others(249): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977604 | ||||||
chr1:977604
|
C | G | 11 | a0001c0001t0001g0104a0001c0001t0001g0178a0001c0001t0001g0183others(8): Show | 12 | HG01099.hp2 HG02559.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150-980G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977604 | ||||||
chr1:977604
|
C | GCAACCCC others(25): Show |
1 | a0002c0002t0002g0013 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2150-980_2150-979i others(34): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977604 | ||||||
chr1:977607
|
AC | A | 20 | a0001c0001t0001g0124a0001c0001t0001g0151a0001c0001t0002g0008others(17): Show | 51 | HG00423.hp1 HG00609.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.2150-984delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977607 | ||||||
chr1:977622
|
TCCC | T | 8 | a0001c0001t0001g0182a0001c0001t0003g0017a0001c0001t0003g0028others(5): Show | 11 | HG00642.hp2 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150-1001_2150-999 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977622 | ||||||
chr1:977626
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(179): Show | 293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2150-1002C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977626 | ||||||
chr1:977626
|
G | GCTCCCCC others(486): Show |
1 | a0016c0037t0009g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2150-1003_2150-100 others(497): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977626 | ||||||
chr1:977628
|
T | C | 8 | a0001c0001t0001g0182a0001c0001t0003g0017a0001c0001t0003g0028others(5): Show | 11 | HG00642.hp2 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150-1004A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977628 | ||||||
chr1:977630
|
C | A | 2 | a0001c0001t0003g0120a0004c0004t0002g0192 | 2 | HG01099.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2150-1006G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977630 | ||||||
chr1:977630
|
CCCCCACC others(203): Show |
C | 2 | a0001c0001t0001g0104a0001c0001t0003g0029 | 3 | HG02976.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2149+1041_2150-100 others(4): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977630 | ||||||
chr1:977632
|
C | G | 8 | a0001c0001t0001g0182a0001c0001t0003g0017a0001c0001t0003g0028others(5): Show | 11 | HG00642.hp2 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150-1008G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977632 | ||||||
chr1:977633
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2150-1009G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977633 | ||||||
chr1:977634
|
CA | C | 9 | a0001c0001t0001g0103a0001c0001t0001g0128a0001c0001t0001g0179others(6): Show | 9 | HG02451.hp1 HG02717.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.2150-1011delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977634 | ||||||
chr1:977635
|
A | ACCAACCC others(120): Show |
1 | a0002c0005t0005g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2150-1012_2150-101 others(131): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977635 | ||||||
chr1:977635
|
A | G | 17 | a0001c0001t0003g0120a0002c0002t0002g0048a0002c0002t0002g0049others(14): Show | 19 | HG01099.hp2 HG02109.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.2150-1011T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977635 | ||||||
chr1:977636
|
C | CCAACCCC others(84): Show |
1 | a0010c0013t0018g0209 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2150-1013_2150-101 others(95): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977636 | ||||||
chr1:977636
|
C | G | 9 | a0001c0001t0001g0103a0001c0001t0001g0128a0001c0001t0001g0179others(6): Show | 9 | HG02451.hp1 HG02717.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.2150-1012G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977636 | ||||||
chr1:977654
|
TCCC | T | 18 | a0001c0001t0001g0151a0001c0001t0002g0008a0001c0001t0002g0105others(15): Show | 49 | HG00423.hp1 HG00609.hp1 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.2150-1033_2150-103 others(7): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977654 | ||||||
chr1:977655
|
C | G | 1 | a0001c0001t0003g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2150-1031G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977655 | ||||||
chr1:977658
|
G | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(167): Show | 252 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.2150-1034C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977658 | ||||||
chr1:977660
|
T | C | 19 | a0001c0001t0001g0151a0001c0001t0002g0008a0001c0001t0002g0105others(16): Show | 50 | HG00423.hp1 HG00609.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.2150-1036A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977660 | ||||||
chr1:977662
|
C | A | 2 | a0001c0001t0003g0120a0004c0004t0002g0192 | 2 | HG01099.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2150-1038G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977662 | ||||||
chr1:977664
|
C | G | 19 | a0001c0001t0001g0151a0001c0001t0002g0008a0001c0001t0002g0105others(16): Show | 50 | HG00423.hp1 HG00609.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.2150-1040G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977664 | ||||||
chr1:977666
|
CA | C | 18 | a0001c0001t0001g0103a0001c0001t0001g0175a0001c0001t0001g0179others(15): Show | 21 | HG00642.hp2 HG01433.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.2150-1043delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977666 | ||||||
chr1:977666
|
CACCAACC others(55): Show |
C | 1 | a0004c0004t0002g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2150-1104_2150-104 others(66): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977666 | ||||||
chr1:977667
|
A | ACCAACCC others(248): Show |
1 | a0002c0005t0005g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2150-1044_2150-104 others(259): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977667 | ||||||
chr1:977667
|
A | C | 1 | a0003c0003t0004g0061 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2150-1043T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977667 | ||||||
chr1:977667
|
A | G | 5 | a0001c0001t0003g0120a0002c0005t0005g0230a0002c0005t0005g0231others(2): Show | 5 | HG01099.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-1043T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977667 | ||||||
chr1:977668
|
C | G | 19 | a0001c0001t0001g0103a0001c0001t0001g0175a0001c0001t0001g0179others(16): Show | 22 | HG00642.hp2 HG01433.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.2150-1044G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977668 | ||||||
chr1:977675
|
C | G | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-1051G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977675 | ||||||
chr1:977676
|
G | A | 1 | a0002c0002t0001g0057 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2150-1052C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977676 | ||||||
chr1:977677
|
G | A | 44 | a0002c0002t0001g0057a0002c0002t0002g0006a0002c0002t0002g0007others(41): Show | 75 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.2150-1053C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977677 | ||||||
chr1:977677
|
G | GGAACCGC others(25): Show |
3 | a0002c0002t0002g0254a0005c0006t0005g0213a0021c0024t0002g0239 | 3 | HG02559.hp1 NA18957.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2150-1054_2150-105 others(36): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977677 | ||||||
chr1:977678
|
G | A | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-1054C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977678 | ||||||
chr1:977679
|
A | C | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-1055T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977679 | ||||||
chr1:977680
|
A | C | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2150-1056T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977680 | ||||||
chr1:977682
|
CGCCTCCC others(170): Show |
C | 1 | a0004c0004t0002g0192 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2149+1022_2150-105 others(4): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977682 | ||||||
chr1:977690
|
G | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(186): Show | 302 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.2150-1066C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977690 | ||||||
chr1:977690
|
G | GCTCCCCC others(761): Show |
1 | a0010c0013t0019g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2150-1067_2150-106 others(772): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977690 | ||||||
chr1:977692
|
T | C | 2 | a0001c0001t0003g0120a0003c0003t0004g0061 | 2 | HG01099.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2150-1068A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977692 | ||||||
chr1:977693
|
C | A | 2 | a0001c0001t0003g0120a0003c0003t0004g0061 | 2 | HG01099.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2150-1069G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977693 | ||||||
chr1:977696
|
C | T | 1 | a0002c0011t0002g0047 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2150-1072G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977696 | ||||||
chr1:977697
|
C | G | 2 | a0001c0001t0001g0175a0006c0008t0001g0085 | 2 | HG01433.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2150-1073G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977697 | ||||||
chr1:977698
|
C | G | 2 | a0001c0001t0003g0120a0003c0003t0004g0061 | 2 | HG01099.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2150-1074G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977698 | ||||||
chr1:977699
|
G | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0172a0001c0001t0001g0235others(2): Show | 5 | HG02523.hp2 HG02723.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-1075C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977699 | ||||||
chr1:977699
|
G | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0003g0120others(1): Show | 4 | HG01099.hp2 HG02132.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-1075C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977699 | ||||||
chr1:977699
|
G | GCCACCCC others(246): Show |
1 | a0002c0005t0005g0233 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2150-1076_2150-107 others(257): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977699 | ||||||
chr1:977699
|
G | GCCACCCC others(117): Show |
1 | a0002c0005t0005g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2150-1076_2150-107 others(128): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977699 | ||||||
chr1:977699
|
GCAACCCC others(22): Show |
G | 1 | a0003c0016t0004g0075 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2150-1104_2150-107 others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977699 | ||||||
chr1:977699
|
GCAACCCC others(52): Show |
G | 2 | a0001c0001t0003g0001a0001c0001t0003g0107 | 3 | NA18962.hp1 NA18999.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2149+1123_2150-107 others(63): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977699 | ||||||
chr1:977699
|
GCAACCCC others(110): Show |
G | 3 | a0001c0001t0003g0112a0001c0001t0014g0116a0001c0031t0001g0097 | 3 | HG02280.hp2 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2149+1065_2150-107 others(4): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977699 | ||||||
chr1:977701
|
A | C | 5 | a0001c0001t0001g0099a0001c0001t0001g0172a0001c0001t0001g0235others(2): Show | 5 | HG02523.hp2 HG03540.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-1077T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977701 | ||||||
chr1:977703
|
C | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0172a0001c0001t0001g0235others(1): Show | 4 | HG02523.hp2 NA19009.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-1079G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977703 | ||||||
chr1:977710
|
A | T | 1 | a0003c0003t0004g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2150-1086T>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977710 | ||||||
chr1:977710
|
AACCGCCT others(22): Show |
A | 1 | a0003c0003t0004g0061 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2150-1115_2150-108 others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977710 | ||||||
chr1:977717
|
T | TCCC | 3 | a0001c0001t0001g0124a0003c0016t0004g0076a0020c0023t0002g0052 | 3 | NA18959.hp2 NA19240.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2150-1094_2150-109 others(7): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977717 | ||||||
chr1:977717
|
TGCC | T | 8 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0003g0001others(5): Show | 13 | HG00609.hp1 HG01361.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.2150-1096_2150-109 others(7): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977717 | ||||||
chr1:977718
|
G | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(203): Show | 323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.2150-1094C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977718 | ||||||
chr1:977719
|
C | CCA | 9 | a0001c0001t0001g0099a0001c0001t0001g0128a0001c0001t0001g0172others(6): Show | 9 | HG00639.hp1 HG01433.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.2150-1096_2150-109 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977719 | ||||||
chr1:977719
|
C | CCACTCCC others(26): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0173others(2): Show | 14 | HG00597.hp2 HG00673.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.2150-1096_2150-109 others(37): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977719 | ||||||
chr1:977719
|
C | CCACTCCC others(123): Show |
1 | a0001c0001t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2150-1096_2150-109 others(134): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977719 | ||||||
chr1:977719
|
C | CCACTCCC others(26): Show |
3 | a0001c0001t0001g0127a0001c0001t0001g0181a0001c0001t0006g0044 | 3 | HG03688.hp1 NA18943.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.2150-1096_2150-109 others(37): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977719 | ||||||
chr1:977719
|
C | CCACTCCC others(89): Show |
1 | a0006c0008t0001g0088 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2150-1096_2150-109 others(100): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977719 | ||||||
chr1:977720
|
C | CA | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(79): Show | 118 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2150-1097_2150-109 others(5): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977720 | ||||||
chr1:977720
|
C | CACT | 20 | a0001c0001t0001g0129a0001c0001t0001g0151a0001c0001t0001g0175others(17): Show | 44 | HG00423.hp1 HG00642.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.2150-1097_2150-109 others(7): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977720 | ||||||
chr1:977720
|
C | T | 3 | a0001c0001t0001g0124a0003c0016t0004g0076a0020c0023t0002g0052 | 3 | NA18959.hp2 NA19240.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2150-1096G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977720 | ||||||
chr1:977721
|
C | A | 87 | a0001c0001t0001g0103a0001c0001t0001g0179a0001c0001t0001g0182others(84): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.2150-1097G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977721 | ||||||
chr1:977721
|
C | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0099others(17): Show | 29 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.2150-1097G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977721 | ||||||
chr1:977722
|
C | A | 1 | a0001c0001t0003g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2150-1098G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977722 | ||||||
chr1:977722
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(79): Show | 118 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2150-1098G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977722 | ||||||
chr1:977724
|
A | AC | 74 | a0002c0002t0002g0006a0002c0002t0002g0007a0002c0002t0002g0010others(71): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2150-1101dupG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977724 | ||||||
chr1:977724
|
A | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(119): Show | 194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2150-1100T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977724 | ||||||
chr1:977724
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2150-1100T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977724 | ||||||
chr1:977724
|
A | T | 1 | a0001c0001t0003g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2150-1100T>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977724 | ||||||
chr1:977724
|
ACCGACCA others(18): Show |
A | 7 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0003g0001others(4): Show | 11 | HG00609.hp1 HG01361.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.2150-1125_2150-110 others(29): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977724 | ||||||
chr1:977724
|
ACCGACCA others(21): Show |
A | 1 | a0003c0003t0004g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2150-1128_2150-110 others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977724 | ||||||
chr1:977724
|
ACCGACCA others(76): Show |
A | 2 | a0001c0001t0003g0001a0001c0001t0003g0102 | 2 | NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2149+1074_2150-110 others(87): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977724 | ||||||
chr1:977725
|
C | CT | 4 | a0002c0002t0001g0057a0002c0002t0002g0013a0002c0002t0002g0056others(1): Show | 6 | HG02809.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150-1102_2150-110 others(5): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977725 | ||||||
chr1:977725
|
CCGACCAA others(50): Show |
C | 2 | a0001c0001t0001g0103a0003c0022t0004g0077 | 2 | HG01256.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2149+1099_2150-110 others(61): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977725 | ||||||
chr1:977725
|
CCGACCAA others(77): Show |
C | 1 | a0001c0001t0003g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2149+1072_2150-110 others(88): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977725 | ||||||
chr1:977725
|
CCGACCAA others(108): Show |
C | 6 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0002g0111others(3): Show | 6 | HG01099.hp2 HG03453.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.2149+1041_2150-110 others(4): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977725 | ||||||
chr1:977727
|
G | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0099others(97): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2150-1103C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977727 | ||||||
chr1:977727
|
G | GCAACCCC others(676): Show |
1 | a0020c0023t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2150-1104_2150-110 others(687): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977727 | ||||||
chr1:977727
|
GAC | G | 19 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0151others(16): Show | 43 | HG00423.hp1 HG00642.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.2150-1105_2150-110 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977727 | ||||||
chr1:977728
|
A | ACCAACCC others(206): Show |
1 | a0010c0013t0018g0209 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2150-1105_2150-110 others(217): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977728 | ||||||
chr1:977728
|
A | ACCAACCC others(614): Show |
2 | a0002c0005t0005g0232a0002c0005t0005g0233 | 2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2150-1105_2150-110 others(625): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977728 | ||||||
chr1:977728
|
A | ACCAACCC others(645): Show |
1 | a0002c0005t0005g0228 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2150-1105_2150-110 others(656): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977728 | ||||||
chr1:977728
|
A | ACCAACCC others(612): Show |
1 | a0002c0005t0005g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2150-1105_2150-110 others(623): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977728 | ||||||
chr1:977728
|
A | ACCAACCC others(644): Show |
10 | a0002c0005t0004g0224a0002c0005t0005g0045a0002c0005t0005g0223others(7): Show | 11 | HG00741.hp1 HG01433.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150-1105_2150-110 others(655): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977728 | ||||||
chr1:977728
|
A | ACCAACCC others(644): Show |
2 | a0002c0005t0005g0230a0002c0005t0005g0231 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-1105_2150-110 others(655): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977728 | ||||||
chr1:977728
|
A | ACCAACCC others(613): Show |
6 | a0002c0005t0008g0046a0002c0005t0008g0227a0005c0006t0005g0214others(3): Show | 7 | HG01891.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-1105_2150-110 others(624): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977728 | ||||||
chr1:977728
|
A | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(79): Show | 118 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2150-1104T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977728 | ||||||
chr1:977728
|
A | G | 79 | a0002c0002t0001g0057a0002c0002t0002g0006a0002c0002t0002g0007others(76): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2150-1104T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977728 | ||||||
chr1:977729
|
C | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(81): Show | 120 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2150-1105G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977729 | ||||||
chr1:977744
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0171 | 3 | HG00438.hp2 NA18990.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2150-1120C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977744 | ||||||
chr1:977748
|
C | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0172a0001c0001t0001g0235others(1): Show | 4 | HG02523.hp2 NA19009.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-1124G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977748 | ||||||
chr1:977751
|
A | ACT | 7 | a0001c0001t0002g0008a0001c0001t0003g0001a0001c0001t0003g0012others(4): Show | 18 | HG00423.hp1 HG01123.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.2150-1128_2150-112 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977751 | ||||||
chr1:977751
|
A | ACTC | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(96): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.2150-1128_2150-112 others(7): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977751 | ||||||
chr1:977751
|
A | ACTCCCCC others(338): Show |
1 | a0001c0001t0001g0129 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2150-1128_2150-112 others(349): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977751 | ||||||
chr1:977751
|
A | ACTCCCCC others(465): Show |
1 | a0001c0001t0001g0130 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2150-1128_2150-112 others(476): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977751 | ||||||
chr1:977751
|
A | C | 5 | a0001c0001t0001g0099a0001c0001t0001g0124a0001c0001t0001g0172others(2): Show | 5 | HG02523.hp2 NA19009.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-1127T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977751 | ||||||
chr1:977751
|
A | T | 7 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0003g0001others(4): Show | 11 | HG00609.hp1 HG01361.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.2150-1127T>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977751 | ||||||
chr1:977752
|
C | CCA | 4 | a0001c0001t0003g0121a0002c0002t0002g0243a0004c0004t0002g0042others(1): Show | 4 | HG00408.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149+1128_2150-112 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977752 | ||||||
chr1:977753
|
C | T | 8 | a0001c0001t0001g0151a0001c0001t0002g0008a0001c0001t0002g0105others(5): Show | 15 | HG01192.hp1 HG01255.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.2149+1128G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977753 | ||||||
chr1:977753
|
CCCCACCA others(78): Show |
C | 2 | a0001c0001t0003g0028a0009c0014t0002g0199 | 3 | NA18954.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2149+1043_2149+112 others(89): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977753 | ||||||
chr1:977754
|
C | A | 3 | a0001c0001t0003g0017a0004c0004t0001g0195a0004c0004t0001g0196 | 5 | HG00642.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2149+1127G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977754 | ||||||
chr1:977754
|
C | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0130a0001c0001t0001g0172others(2): Show | 5 | HG02132.hp2 HG02523.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.2149+1127G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977754 | ||||||
chr1:977754
|
CCCACCAA others(79): Show |
C | 1 | a0001c0001t0003g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2149+1041_2149+112 others(90): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977754 | ||||||
chr1:977755
|
CCACCAAC others(78): Show |
C | 7 | a0001c0001t0001g0151a0001c0001t0002g0008a0001c0001t0002g0105others(4): Show | 14 | HG01192.hp1 HG01255.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.2149+1041_2149+112 others(89): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977755 | ||||||
chr1:977756
|
CACCAACC others(107): Show |
C | 3 | a0001c0001t0003g0017a0004c0004t0001g0195a0004c0004t0001g0196 | 5 | HG00642.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2149+1011_2149+112 others(4): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977756 | ||||||
chr1:977757
|
A | C | 11 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0003g0001others(8): Show | 29 | HG00423.hp1 HG00609.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.2149+1124T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977757 | ||||||
chr1:977757
|
A | G | 10 | a0001c0001t0003g0121a0002c0002t0002g0243a0003c0003t0004g0063others(7): Show | 10 | HG00408.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2149+1124T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977757 | ||||||
chr1:977758
|
C | G | 11 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0003g0001others(8): Show | 29 | HG00423.hp1 HG00609.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.2149+1123G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977758 | ||||||
chr1:977762
|
C | A | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2149+1119G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977762 | ||||||
chr1:977766
|
G | C | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2149+1115C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977766 | ||||||
chr1:977780
|
A | ACC | 9 | a0001c0001t0002g0008a0001c0001t0003g0001a0001c0001t0003g0012others(6): Show | 19 | HG00408.hp2 HG00423.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.2149+1100_2149+110 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977780 | ||||||
chr1:977780
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2149+1101T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977780 | ||||||
chr1:977780
|
AATCCCCC others(77): Show |
A | 1 | a0001c0001t0003g0001 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2149+1017_2149+110 others(88): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977780 | ||||||
chr1:977781
|
A | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(111): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.2149+1100T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977781 | ||||||
chr1:977782
|
T | C | 9 | a0001c0001t0002g0008a0001c0001t0003g0001a0001c0001t0003g0012others(6): Show | 19 | HG00408.hp2 HG00423.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.2149+1099A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977782 | ||||||
chr1:977786
|
C | A | 2 | a0001c0001t0013g0115a0004c0004t0015g0197 | 2 | NA19056.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2149+1095G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977786 | ||||||
chr1:977786
|
C | CCCA | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(87): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.2149+1092_2149+109 others(7): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977786 | ||||||
chr1:977786
|
C | CCCACCAA others(27): Show |
3 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0266 | 3 | HG01070.hp2 HG01168.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2149+1094_2149+109 others(38): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977786 | ||||||
chr1:977786
|
C | G | 11 | a0001c0001t0001g0103a0001c0001t0002g0008a0001c0001t0003g0001others(8): Show | 21 | HG00408.hp2 HG00423.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.2149+1095G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977786 | ||||||
chr1:977787
|
C | CCG | 17 | a0001c0001t0001g0099a0001c0001t0001g0124a0001c0001t0001g0129others(14): Show | 23 | HG00609.hp1 HG01361.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.2149+1093_2149+109 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977787 | ||||||
chr1:977789
|
AACCCCGG others(44): Show |
A | 1 | a0004c0004t0015g0197 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2149+1041_2149+109 others(55): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977789 | ||||||
chr1:977791
|
C | A | 2 | a0001c0001t0001g0177a0006c0008t0001g0088 | 2 | HG00280.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.2149+1090G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977791 | ||||||
chr1:977801
|
T | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(195): Show | 310 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.2149+1080A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977801 | ||||||
chr1:977806
|
C | G | 5 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0186others(2): Show | 5 | HG01070.hp2 HG01168.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.2149+1075G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977806 | ||||||
chr1:977809
|
A | ACCACCCC others(27): Show |
1 | a0010c0013t0019g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2149+1071_2149+107 others(38): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977809
|
A | ACT | 8 | a0001c0001t0001g0099a0001c0001t0001g0124a0001c0001t0001g0130others(5): Show | 9 | HG02132.hp2 HG02523.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.2149+1071_2149+107 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977809
|
A | ACTC | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(81): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.2149+1071_2149+107 others(7): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977809
|
A | ACTCCCCC others(59): Show |
1 | a0001c0001t0001g0002 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2149+1071_2149+107 others(70): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977809
|
A | ACTCCCCC others(88): Show |
7 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0122others(4): Show | 8 | HG02074.hp2 HG02129.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2149+1071_2149+107 others(99): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977809
|
A | ACTCCCCC others(57): Show |
1 | a0006c0008t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2149+1071_2149+107 others(68): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977809
|
A | ACTCCCCC others(183): Show |
1 | a0004c0004t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2149+1071_2149+107 others(194): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977809
|
A | ACTCCCCC others(431): Show |
1 | a0010c0013t0018g0209 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2149+1071_2149+107 others(442): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977809
|
A | C | 5 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0186others(2): Show | 5 | HG01070.hp2 HG01168.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.2149+1072T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977809
|
A | T | 2 | a0001c0001t0003g0001a0001c0001t0003g0102 | 2 | NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2149+1072T>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977809 | ||||||
chr1:977810
|
C | A | 1 | a0003c0003t0004g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2149+1071G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977810 | ||||||
chr1:977810
|
C | CCA | 14 | a0001c0001t0001g0103a0001c0001t0002g0008a0001c0001t0002g0106others(11): Show | 31 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.2149+1070_2149+107 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977810 | ||||||
chr1:977811
|
C | T | 1 | a0003c0003t0004g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2149+1070G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977811 | ||||||
chr1:977812
|
C | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0122others(11): Show | 15 | HG01070.hp2 HG01168.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.2149+1069G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977812 | ||||||
chr1:977815
|
A | C | 12 | a0001c0001t0001g0099a0001c0001t0001g0124a0001c0001t0001g0130others(9): Show | 14 | HG02132.hp2 HG02523.hp2 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.2149+1066T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977815 | ||||||
chr1:977815
|
A | G | 14 | a0001c0001t0001g0103a0001c0001t0002g0008a0001c0001t0002g0106others(11): Show | 31 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.2149+1066T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977815 | ||||||
chr1:977816
|
C | CCAACCCC others(84): Show |
3 | a0001c0001t0001g0002a0001c0001t0001g0177a0006c0008t0001g0088 | 3 | HG00280.hp2 HG01109.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2149+1064_2149+106 others(95): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977816 | ||||||
chr1:977816
|
C | G | 14 | a0001c0001t0001g0099a0001c0001t0001g0124a0001c0001t0001g0130others(11): Show | 20 | HG01358.hp2 HG01943.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2149+1065G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977816 | ||||||
chr1:977817
|
C | G | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2149+1064G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977817 | ||||||
chr1:977818
|
A | C | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2149+1063T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977818 | ||||||
chr1:977820
|
C | A | 1 | a0001c0007t0001g0092 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2149+1061G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977820 | ||||||
chr1:977838
|
A | ACC | 14 | a0001c0001t0001g0103a0001c0001t0002g0008a0001c0001t0003g0001others(11): Show | 30 | HG00408.hp2 HG00423.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.2149+1042_2149+104 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977838 | ||||||
chr1:977838
|
A | G | 1 | a0001c0001t0013g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2149+1043T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977838 | ||||||
chr1:977838
|
AATCCCCC others(19): Show |
A | 7 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0003g0001others(4): Show | 11 | HG00609.hp1 HG01361.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.2149+1017_2149+104 others(30): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977838 | ||||||
chr1:977838
|
AATCCCCC others(110): Show |
A | 1 | a0004c0004t0002g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2149+926_2149+1042 others(3): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977838 | ||||||
chr1:977839
|
A | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(111): Show | 162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2149+1042T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977839 | ||||||
chr1:977840
|
T | C | 17 | a0001c0001t0001g0103a0001c0001t0002g0008a0001c0001t0003g0001others(14): Show | 34 | HG00408.hp2 HG00423.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.2149+1041A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977840 | ||||||
chr1:977844
|
C | A | 1 | a0003c0022t0004g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2149+1037G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977844 | ||||||
chr1:977844
|
C | CCCACCAA others(25): Show |
1 | a0006c0008t0001g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2149+1036_2149+103 others(36): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977844 | ||||||
chr1:977844
|
C | CCCACCAA others(149): Show |
1 | a0001c0001t0001g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2149+1036_2149+103 others(160): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977844 | ||||||
chr1:977844
|
C | CGCGCAAC others(277): Show |
1 | a0001c0001t0001g0183 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2149+1036_2149+103 others(288): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977844 | ||||||
chr1:977844
|
C | G | 22 | a0001c0001t0001g0103a0001c0001t0001g0179a0001c0001t0001g0182others(19): Show | 40 | HG00408.hp2 HG00423.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.2149+1037G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977844 | ||||||
chr1:977845
|
C | CCACCAAC others(150): Show |
1 | a0001c0001t0001g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2149+1035_2149+103 others(161): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977845
|
C | CCACCAAC others(119): Show |
1 | a0001c0001t0001g0039 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2149+1035_2149+103 others(130): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977845
|
C | CCACCAAC others(180): Show |
1 | a0001c0001t0006g0207 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2149+1035_2149+103 others(191): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977845
|
C | CCACCAAC others(181): Show |
9 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0040others(6): Show | 9 | HG00438.hp2 HG00609.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.2149+1035_2149+103 others(192): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977845
|
C | CCACCAAC others(182): Show |
1 | a0001c0001t0006g0206 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2149+1035_2149+103 others(193): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977845
|
C | CCACCAAC others(149): Show |
1 | a0001c0001t0017g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2149+1035_2149+103 others(160): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977845
|
C | CCACCAAC others(118): Show |
4 | a0001c0001t0001g0180a0001c0001t0001g0181a0006c0008t0001g0090others(1): Show | 4 | HG00099.hp1 HG02486.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+1035_2149+103 others(129): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977845
|
C | CCACCAAC others(149): Show |
66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(63): Show | 106 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.2149+1035_2149+103 others(160): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977845
|
C | CCG | 27 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0036others(24): Show | 28 | HG00280.hp2 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2149+1035_2149+103 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977845
|
C | G | 20 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0117others(17): Show | 33 | HG00673.hp2 HG01192.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.2149+1036G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977845 | ||||||
chr1:977849
|
C | A | 1 | a0001c0001t0001g0178 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2149+1032G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977849 | ||||||
chr1:977859
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(223): Show | 355 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.2149+1022A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977859 | ||||||
chr1:977867
|
A | ACT | 16 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(13): Show | 17 | HG00639.hp1 HG01070.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.2149+1013_2149+101 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977867 | ||||||
chr1:977868
|
C | A | 1 | a0003c0022t0004g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2149+1013G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977868 | ||||||
chr1:977869
|
C | T | 1 | a0003c0022t0004g0077 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2149+1012G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977869 | ||||||
chr1:977869
|
CA | C | 7 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0003g0001others(4): Show | 12 | HG00609.hp1 HG01361.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.2149+1011delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977869 | ||||||
chr1:977870
|
A | C | 19 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(16): Show | 20 | HG00639.hp1 HG01070.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.2149+1011T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977870 | ||||||
chr1:977873
|
C | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0178 | 2 | NA18961.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2149+1008G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977873 | ||||||
chr1:977873
|
C | CCG | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(129): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.2149+1007_2149+100 others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977873 | ||||||
chr1:977873
|
C | G | 10 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0003g0001others(7): Show | 17 | HG00609.hp1 HG00642.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.2149+1008G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977873 | ||||||
chr1:977874
|
C | CCAACCCC others(84): Show |
1 | a0001c0001t0001g0178 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2149+1006_2149+100 others(95): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977874 | ||||||
chr1:977874
|
C | G | 16 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(13): Show | 17 | HG00639.hp1 HG01070.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.2149+1007G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977874 | ||||||
chr1:977874
|
CCAACCCC others(82): Show |
C | 7 | a0001c0001t0002g0008a0001c0001t0003g0001a0001c0001t0003g0012others(4): Show | 17 | HG00408.hp2 HG00423.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.2149+918_2149+1006 others(92): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977874 | ||||||
chr1:977898
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(136): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2149+983A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977898 | ||||||
chr1:977899
|
C | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(136): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2149+982G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977899 | ||||||
chr1:977900
|
C | A | 2 | a0001c0001t0001g0103a0004c0025t0004g0060 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2149+981G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977900 | ||||||
chr1:977901
|
C | A | 1 | a0003c0003t0004g0073 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2149+980G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977901 | ||||||
chr1:977904
|
C | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(136): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2149+977G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977904 | ||||||
chr1:977905
|
G | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(137): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.2149+976C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977905 | ||||||
chr1:977905
|
GCAACCCC others(52): Show |
G | 1 | a0001c0001t0001g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2149+917_2149+975d others(61): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977905 | ||||||
chr1:977926
|
CACCACCC others(83): Show |
C | 1 | a0004c0025t0004g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2149+865_2149+954d others(92): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977926 | ||||||
chr1:977930
|
A | C | 2 | a0001c0001t0001g0129a0003c0003t0004g0073 | 2 | HG02155.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2149+951T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977930 | ||||||
chr1:977933
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2149+948G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977933 | ||||||
chr1:977935
|
G | GC | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(149): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2149+945dupG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977935 | ||||||
chr1:977935
|
GCAACCCC others(23): Show |
G | 20 | a0003c0003t0004g0014a0003c0003t0004g0015a0003c0003t0004g0021others(17): Show | 29 | HG00323.hp1 HG00558.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.2149+916_2149+945d others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977935 | ||||||
chr1:977937
|
A | C | 1 | a0001c0001t0003g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2149+944T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977937 | ||||||
chr1:977939
|
C | A | 1 | a0001c0001t0003g0185 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2149+942G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977939 | ||||||
chr1:977942
|
C | T | 10 | a0004c0004t0001g0195a0004c0004t0001g0196a0004c0004t0002g0004others(7): Show | 14 | HG01358.hp2 HG01943.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2149+939G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977942 | ||||||
chr1:977943
|
GGGAACCG others(52): Show |
G | 12 | a0003c0003t0004g0009a0003c0003t0004g0026a0003c0003t0004g0055others(9): Show | 17 | HG00140.hp2 HG00735.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.2149+879_2149+937d others(61): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977943 | ||||||
chr1:977949
|
C | T | 13 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0002g0111others(10): Show | 21 | HG00609.hp1 HG00642.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.2149+932G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977949 | ||||||
chr1:977954
|
G | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(129): Show | 196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2149+927C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977954 | ||||||
chr1:977954
|
GC | G | 26 | a0001c0001t0001g0041a0001c0001t0001g0179a0001c0001t0001g0182others(23): Show | 39 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2149+926delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977954 | ||||||
chr1:977957
|
C | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(128): Show | 195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.2149+924G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977957 | ||||||
chr1:977957
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2149+924G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977957 | ||||||
chr1:977958
|
C | A | 1 | a0004c0004t0002g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2149+923G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977958 | ||||||
chr1:977960
|
A | AC | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(127): Show | 194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2149+920dupG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977960 | ||||||
chr1:977960
|
A | C | 2 | a0001c0001t0001g0129a0004c0004t0002g0198 | 2 | HG02717.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2149+921T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977960 | ||||||
chr1:977963
|
G | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(152): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.2149+918C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977963 | ||||||
chr1:977964
|
A | C | 1 | a0003c0003t0004g0073 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2149+917T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977964 | ||||||
chr1:977964
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(130): Show | 211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.2149+917T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977964 | ||||||
chr1:977965
|
C | G | 1 | a0003c0003t0004g0073 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2149+916G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977965 | ||||||
chr1:977972
|
C | T | 6 | a0004c0004t0002g0004a0004c0004t0002g0042a0004c0004t0002g0198others(3): Show | 11 | HG00408.hp2 HG00673.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.2149+909G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977972 | ||||||
chr1:977973
|
GGGAACCG others(22): Show |
G | 24 | a0001c0001t0001g0041a0001c0001t0001g0179a0001c0001t0001g0182others(21): Show | 37 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2149+879_2149+907d others(31): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977973 | ||||||
chr1:977979
|
C | T | 25 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0114others(22): Show | 50 | HG00423.hp1 HG01123.hp1 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.2149+902G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977979 | ||||||
chr1:977984
|
C | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(118): Show | 195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.2149+897G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977984 | ||||||
chr1:977987
|
A | ACCACCCC others(57): Show |
1 | a0006c0008t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2149+893_2149+894i others(66): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977987 | ||||||
chr1:977987
|
A | ACCACCCC others(56): Show |
1 | a0001c0001t0001g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2149+893_2149+894i others(65): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977987 | ||||||
chr1:977987
|
A | ACCACCCC others(55): Show |
14 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0039others(11): Show | 15 | HG00639.hp1 HG01070.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.2149+893_2149+894i others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977987 | ||||||
chr1:977987
|
A | ACCACCCC others(55): Show |
1 | a0004c0004t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2149+893_2149+894i others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977987 | ||||||
chr1:977987
|
A | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(118): Show | 195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.2149+894T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977987 | ||||||
chr1:977987
|
AATCCCCC others(21): Show |
A | 2 | a0001c0001t0003g0102a0004c0004t0002g0191 | 2 | NA19009.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2149+866_2149+893d others(30): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977987 | ||||||
chr1:977988
|
A | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(132): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.2149+893T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977988 | ||||||
chr1:977989
|
T | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(131): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.2149+892A>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977989 | ||||||
chr1:977989
|
T | TCCCCCCA others(24): Show |
1 | a0020c0023t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2149+861_2149+891d others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977989 | ||||||
chr1:977989
|
TCCCCCCA others(23): Show |
T | 21 | a0003c0003t0004g0014a0003c0003t0004g0015a0003c0003t0004g0021others(18): Show | 30 | HG00323.hp1 HG00558.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.2149+862_2149+891d others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977989 | ||||||
chr1:977993
|
C | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(132): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.2149+888G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977993 | ||||||
chr1:977993
|
C | CCCACCAA others(366): Show |
1 | a0001c0001t0001g0129 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2149+887_2149+888i others(375): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977993 | ||||||
chr1:977999
|
C | T | 4 | a0002c0002t0001g0057a0002c0002t0002g0013a0002c0002t0002g0056others(1): Show | 6 | HG02809.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2149+882G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 977999 | ||||||
chr1:978002
|
A | AGGAACCG others(2123): Show |
1 | a0017c0029t0001g0086 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2149+878_2149+879i others(2132): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978002 | ||||||
chr1:978002
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(133): Show | 214 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.2149+879T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978002 | ||||||
chr1:978017
|
A | C | 2 | a0001c0001t0003g0102a0004c0004t0002g0191 | 2 | NA19009.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2149+864T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978017 | ||||||
chr1:978017
|
AC | A | 12 | a0003c0003t0004g0009a0003c0003t0004g0026a0003c0003t0004g0055others(9): Show | 17 | HG00140.hp2 HG00735.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.2149+863delG | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978017 | ||||||
chr1:978018
|
C | A | 1 | a0004c0025t0004g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2149+863G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978018 | ||||||
chr1:978018
|
C | CCCCCCCC others(22): Show |
39 | a0002c0002t0001g0057a0002c0002t0002g0006a0002c0002t0002g0007others(36): Show | 70 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.2149+834_2149+862d others(31): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978018 | ||||||
chr1:978019
|
C | T | 13 | a0003c0003t0004g0009a0003c0003t0004g0026a0003c0003t0004g0055others(10): Show | 18 | HG00140.hp2 HG00735.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2149+862G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978019 | ||||||
chr1:978032
|
A | G | 17 | a0003c0003t0004g0062a0004c0004t0001g0195a0004c0004t0001g0196others(14): Show | 27 | HG00408.hp2 HG00673.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.2149+849T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978032 | ||||||
chr1:978045
|
CA | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(151): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.2149+835delT | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978045 | ||||||
chr1:978047
|
A | ACCCCCCC others(23): Show |
1 | a0002c0002t0002g0241 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2149+833_2149+834i others(32): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978047 | ||||||
chr1:978047
|
A | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0003g0028others(3): Show | 7 | HG03490.hp2 NA18954.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.2149+834T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978047 | ||||||
chr1:978049
|
C | G | 2 | a0001c0001t0001g0100a0005c0006t0005g0211 | 2 | NA19002.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2149+832G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978049 | ||||||
chr1:978093
|
C | T | 1 | a0016c0037t0009g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2149+788G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978093 | ||||||
chr1:978132
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2149+749G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978132 | ||||||
chr1:978176
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2149+705G>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978176 | ||||||
chr1:978206
|
G | GAACT | 7 | a0002c0005t0004g0224a0002c0005t0005g0045a0002c0005t0005g0222others(4): Show | 8 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2149+671_2149+674d others(6): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978206 | ||||||
chr1:978210
|
TGCCTGCC others(24): Show |
T | 1 | a0001c0001t0003g0016 | 3 | NA18975.hp2 NA18998.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2149+640_2149+670d others(33): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978210 | ||||||
chr1:978225
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2149+656G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978225 | ||||||
chr1:978230
|
G | A | 41 | a0002c0002t0001g0057a0002c0002t0002g0006a0002c0002t0002g0007others(38): Show | 72 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.2149+651C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978230 | ||||||
chr1:978234
|
C | T | 1 | a0023c0017t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2149+647G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978234 | ||||||
chr1:978318
|
C | T | 7 | a0002c0005t0004g0224a0002c0005t0005g0045a0002c0005t0005g0222others(4): Show | 8 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2149+563G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978318 | ||||||
chr1:978334
|
C | G | 1 | a0001c0031t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2149+547G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978334 | ||||||
chr1:978373
|
G | A | 1 | a0010c0013t0018g0209 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2149+508C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978373 | ||||||
chr1:978509
|
G | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(140): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.2149+372C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978509 | ||||||
chr1:978773
|
A | G | 1 | a0002c0002t0002g0240 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2149+108T>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978773 | ||||||
chr1:978812
|
G | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(241): Show | 384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.2149+69C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2/3 | chr1 | 978812 | ||||||
chr1:981210
|
G | A | 9 | a0001c0028t0004g0080a0003c0003t0004g0009a0003c0003t0004g0015others(6): Show | 17 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-144-37C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981210 | ||||||
chr1:981282
|
A | C | 43 | a0002c0002t0001g0057a0002c0002t0002g0006a0002c0002t0002g0007others(40): Show | 74 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.-144-109T>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981282 | ||||||
chr1:981287
|
C | T | 3 | a0003c0003t0004g0021a0003c0003t0004g0054a0003c0003t0004g0055 | 4 | HG01109.hp1 HG02055.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-144-114G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981287 | ||||||
chr1:981454
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(156): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-144-281C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981454 | ||||||
chr1:981458
|
G | A | 2 | a0010c0013t0018g0209a0010c0013t0019g0210 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-144-285C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981458 | ||||||
chr1:981596
|
G | A | 2 | a0010c0013t0018g0209a0010c0013t0019g0210 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-144-423C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981596 | ||||||
chr1:981680
|
C | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(237): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.-145+385G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981680 | ||||||
chr1:981743
|
C | T | 1 | a0008c0012t0002g0053 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-145+322G>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981743 | ||||||
chr1:981783
|
G | T | 1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-145+282C>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981783 | ||||||
chr1:981784
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-145+281G>C | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981784 | ||||||
chr1:981787
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-145+278C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981787 | ||||||
chr1:981924
|
G | A | 1 | a0003c0003t0004g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-145+141C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981924 | ||||||
chr1:981935
|
G | A | 40 | a0001c0001t0001g0266a0002c0002t0002g0006a0002c0002t0002g0007others(37): Show | 69 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.-145+130C>T | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981935 | ||||||
chr1:981985
|
T | C | 1 | a0020c0023t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-145+80A>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981985 | ||||||
chr1:981986
|
G | C | 1 | a0020c0023t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-145+79C>G | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981986 | ||||||
chr1:981987
|
G | T | 1 | a0020c0023t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-145+78C>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 981987 | ||||||
chr1:982010
|
G | T | 1 | a0003c0003t0004g0051 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-145+55C>A | PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 1/3 | chr1 | 982010 |