geneid | 731 |
---|---|
ensemblid | ENSG00000157131.12 |
hgncid | 1352 |
symbol | C8A |
name | complement C8 alpha chain |
refseq_nuc | NM_000562.3 |
refseq_prot | NP_000553.1 |
ensembl_nuc | ENST00000361249.4 |
ensembl_prot | ENSP00000354458.3 |
mane_status | MANE Select |
chr | chr1 |
start | 56854797 |
end | 56918223 |
strand | + |
ver | v1.2 |
region | chr1:56854797-56918223 |
region5000 | chr1:56849797-56923223 |
regionname0 | C8A_chr1_56854797_56918223 |
regionname5000 | C8A_chr1_56849797_56923223 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 584 | 185 | 48 | 32 | 87 | 7 | 10 | 70 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0002 | 0/1 | 584 | 99 | 5 | 12 | 54 | 6 | 21 | 40 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0003 | 0/0 | 584 | 20 | 12 | 5 | 1 | 0 | 2 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0004 | 0/0 | 584 | 17 | 3 | 1 | 10 | 1 | 2 | 7 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0005 | 0/0 | 584 | 12 | 7 | 0 | 5 | 0 | 0 | 4 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0006 | 0/0 | 584 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0007 | 0/0 | 584 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0008 | 0/0 | 584 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0009 | 0/0 | 584 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0010 | 0/0 | 584 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0011 | 0/0 | 584 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0012 | 0/0 | 584 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0013 | 0/0 | 584 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0014 | 0/0 | 584 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0015 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0016 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0017 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0018 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0019 | 0/0 | 584 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0020 | 0/0 | 584 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1755 | 180 | 45 | 31 | 86 | 7 | 10 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0002 | 0/1 | 1755 | 99 | 5 | 12 | 54 | 6 | 21 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0003 | 0/0 | 1755 | 20 | 12 | 5 | 1 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0004 | 0/0 | 1755 | 17 | 3 | 1 | 10 | 1 | 2 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0005 | 0/0 | 1755 | 9 | 4 | 0 | 5 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0006 | 0/0 | 1755 | 9 | 9 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0007 | 0/0 | 1755 | 4 | 0 | 0 | 0 | 0 | 4 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0008 | 0/0 | 1755 | 4 | 0 | 4 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0009 | 0/0 | 1755 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0010 | 0/0 | 1755 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0011 | 0/0 | 1755 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0012 | 0/0 | 1755 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0013 | 0/0 | 1755 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0014 | 0/0 | 1755 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0015 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0016 | 0/0 | 1755 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0017 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0018 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0019 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0020 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0021 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0022 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0023 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
c0024 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 613 | 313 | 58 | 51 | 154 | 14 | 34 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
t0002 | 0/0 | 613 | 37 | 22 | 7 | 6 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
t0003 | 0/0 | 613 | 7 | 7 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
t0004 | 0/0 | 613 | 4 | 0 | 0 | 0 | 0 | 4 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
t0005 | 0/0 | 613 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
t0006 | 0/0 | 613 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
t0007 | 0/0 | 613 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0002 | 0/0 | 8 | 1 | 1 | 2 | 0 | 4 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0048 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1755 | 180 | 45 | 31 | 86 | 7 | 10 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0001c0010 | 0/0 | 1755 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0001c0018 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0001c0023 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0002c0002 | 0/1 | 1755 | 99 | 5 | 12 | 54 | 6 | 21 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0003c0003 | 0/0 | 1755 | 20 | 12 | 5 | 1 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0004c0004 | 0/0 | 1755 | 17 | 3 | 1 | 10 | 1 | 2 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0005c0005 | 0/0 | 1755 | 9 | 4 | 0 | 5 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0005c0009 | 0/0 | 1755 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0006c0006 | 0/0 | 1755 | 9 | 9 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0007c0007 | 0/0 | 1755 | 4 | 0 | 0 | 0 | 0 | 4 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0008c0008 | 0/0 | 1755 | 4 | 0 | 4 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0009c0013 | 0/0 | 1755 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0010c0012 | 0/0 | 1755 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0011c0014 | 0/0 | 1755 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0012c0011 | 0/0 | 1755 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0013c0016 | 0/0 | 1755 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0014c0022 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0015c0021 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0016c0019 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0017c0020 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0018c0017 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0019c0015 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0020c0024 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2367 | 171 | 36 | 31 | 86 | 7 | 10 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0001c0001t0003 | 0/0 | 2367 | 7 | 7 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0001c0001t0005 | 0/0 | 2367 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0001c0010t0001 | 0/0 | 2367 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0001c0018t0001 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0001c0023t0001 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0002c0002t0001 | 0/1 | 2367 | 98 | 5 | 12 | 53 | 6 | 21 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0002c0002t0006 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0003c0003t0002 | 0/0 | 2367 | 20 | 12 | 5 | 1 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0004c0004t0001 | 0/0 | 2367 | 17 | 3 | 1 | 10 | 1 | 2 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0005c0005t0002 | 0/0 | 2367 | 9 | 4 | 0 | 5 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0005c0009t0002 | 0/0 | 2367 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0006c0006t0001 | 0/0 | 2367 | 9 | 9 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0007c0007t0004 | 0/0 | 2367 | 4 | 0 | 0 | 0 | 0 | 4 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0008c0008t0001 | 0/0 | 2367 | 4 | 0 | 4 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0009c0013t0002 | 0/0 | 2367 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0010c0012t0001 | 0/0 | 2367 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0011c0014t0001 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0012c0011t0001 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0013c0016t0001 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0014c0022t0002 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0015c0021t0001 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0016c0019t0001 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0017c0020t0005 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0018c0017t0002 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0019c0015t0007 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
a0020c0024t0002 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | copy fasta | chr1 | 56849797 | 56923223 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 1 | 1 | 2 | 0 | 3 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0010t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0010t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0010t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0018t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0001c0023t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0002c0002t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0003c0003t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0004c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0005t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0005t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0005t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0005t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0005t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0005t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0005t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0005t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0009t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0005c0009t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0006c0006t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0006c0006t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0006c0006t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0006c0006t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0006c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0006c0006t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0006c0006t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0006c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0007c0007t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0007c0007t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0007c0007t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0007c0007t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0008c0008t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0008c0008t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0008c0008t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0008c0008t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0009c0013t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0009c0013t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0010c0012t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0010c0012t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0011c0014t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0012c0011t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0012c0011t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0013c0016t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0014c0022t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0015c0021t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0016c0019t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0017c0020t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0018c0017t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0019c0015t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
a0020c0024t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0004 | c0004 | t0001 | g0232 | EUR | FIN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0057 | EUR | FIN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00408 | hp1 | a0004 | c0004 | t0001 | g0043 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00408 | hp2 | a0011 | c0014 | t0001 | g0014 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00558 | hp2 | a0004 | c0004 | t0001 | g0247 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG00738 | hp2 | a0010 | c0012 | t0001 | g0204 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01081 | hp1 | a0010 | c0012 | t0001 | g0176 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01106 | hp2 | a0004 | c0004 | t0001 | g0233 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01109 | hp1 | a0003 | c0003 | t0002 | g0198 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01109 | hp2 | a0003 | c0003 | t0002 | g0081 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01192 | hp2 | a0001 | c0023 | t0001 | g0071 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01243 | hp2 | a0014 | c0022 | t0002 | g0220 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01346 | hp1 | a0003 | c0003 | t0002 | g0252 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01346 | hp2 | a0008 | c0008 | t0001 | g0261 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01358 | hp1 | a0008 | c0008 | t0001 | g0248 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01496 | hp2 | a0008 | c0008 | t0001 | g0262 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0036 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0032 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0036 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01891 | hp1 | a0003 | c0003 | t0002 | g0041 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01943 | hp1 | a0003 | c0003 | t0002 | g0094 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01975 | hp1 | a0020 | c0024 | t0002 | g0260 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0212 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02004 | hp2 | a0008 | c0008 | t0001 | g0259 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02015 | hp2 | a0005 | c0005 | t0002 | g0167 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02040 | hp2 | a0003 | c0003 | t0002 | g0238 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02055 | hp2 | a0004 | c0004 | t0001 | g0245 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02080 | hp2 | a0004 | c0004 | t0001 | g0271 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02145 | hp1 | a0003 | c0003 | t0002 | g0255 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02145 | hp2 | a0003 | c0003 | t0002 | g0281 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CDX | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | CDX | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0147 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02280 | hp2 | a0003 | c0003 | t0002 | g0016 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02451 | hp2 | a0005 | c0005 | t0002 | g0206 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02615 | hp1 | a0001 | c0010 | t0001 | g0264 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02622 | hp2 | a0018 | c0017 | t0002 | g0079 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02630 | hp2 | a0006 | c0006 | t0001 | g0087 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02647 | hp1 | a0005 | c0005 | t0002 | g0200 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02698 | hp2 | a0013 | c0016 | t0001 | g0002 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02735 | hp2 | a0007 | c0007 | t0004 | g0054 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0029 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02809 | hp1 | a0005 | c0009 | t0002 | g0205 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02818 | hp1 | a0017 | c0020 | t0005 | g0270 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02895 | hp1 | a0006 | c0006 | t0001 | g0047 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02896 | hp1 | a0009 | c0013 | t0002 | g0175 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02897 | hp1 | a0009 | c0013 | t0002 | g0174 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02897 | hp2 | a0006 | c0006 | t0001 | g0047 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02922 | hp2 | a0005 | c0005 | t0002 | g0199 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02965 | hp1 | a0006 | c0006 | t0001 | g0082 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02965 | hp2 | a0003 | c0003 | t0002 | g0041 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02976 | hp1 | a0003 | c0003 | t0002 | g0228 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03041 | hp2 | a0006 | c0006 | t0001 | g0266 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03098 | hp1 | a0006 | c0006 | t0001 | g0089 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03098 | hp2 | a0015 | c0021 | t0001 | g0072 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03130 | hp1 | a0003 | c0003 | t0002 | g0223 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03139 | hp1 | a0004 | c0004 | t0001 | g0039 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03209 | hp1 | a0016 | c0019 | t0001 | g0209 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03225 | hp2 | a0004 | c0004 | t0001 | g0039 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03490 | hp1 | a0003 | c0003 | t0002 | g0040 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0091 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03492 | hp1 | a0003 | c0003 | t0002 | g0040 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03669 | hp2 | a0007 | c0007 | t0004 | g0052 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0184 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03831 | hp2 | a0007 | c0007 | t0004 | g0055 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0158 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03942 | hp2 | a0004 | c0004 | t0001 | g0246 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0160 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG04228 | hp1 | a0007 | c0007 | t0004 | g0056 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0140 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18522 | hp1 | a0001 | c0010 | t0001 | g0263 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0250 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18747 | hp2 | a0019 | c0015 | t0007 | g0053 | EAS | CHB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18906 | hp2 | a0006 | c0006 | t0001 | g0215 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18939 | hp2 | a0012 | c0011 | t0001 | g0243 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18940 | hp2 | a0005 | c0005 | t0002 | g0182 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18952 | hp2 | a0004 | c0004 | t0001 | g0043 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18961 | hp1 | a0005 | c0005 | t0002 | g0181 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18968 | hp2 | a0012 | c0011 | t0001 | g0244 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18977 | hp1 | a0005 | c0005 | t0002 | g0113 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18980 | hp1 | a0005 | c0005 | t0002 | g0187 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18993 | hp1 | a0004 | c0004 | t0001 | g0239 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18995 | hp1 | a0002 | c0002 | t0006 | g0034 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19007 | hp1 | a0011 | c0014 | t0001 | g0014 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19030 | hp2 | a0003 | c0003 | t0002 | g0219 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19066 | hp1 | a0004 | c0004 | t0001 | g0045 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19080 | hp1 | a0001 | c0018 | t0001 | g0123 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19080 | hp2 | a0004 | c0004 | t0001 | g0241 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19084 | hp2 | a0004 | c0004 | t0001 | g0045 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19090 | hp2 | a0004 | c0004 | t0001 | g0240 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19240 | hp1 | a0003 | c0003 | t0002 | g0016 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA19240 | hp2 | a0005 | c0005 | t0002 | g0201 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ASW | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20129 | hp2 | a0003 | c0003 | t0002 | g0279 | AFR | ASW | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0258 | EUR | TSI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0190 | EUR | TSI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0179 | EUR | TSI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | TSI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0196 | SAS | GIH | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20905 | hp2 | a0004 | c0004 | t0001 | g0269 | SAS | GIH | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG01123 | hp2 | a0003 | c0003 | t0002 | g0104 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02486 | hp1 | a0003 | c0003 | t0002 | g0280 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02486 | hp2 | a0005 | c0009 | t0002 | g0037 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02559 | hp1 | a0001 | c0010 | t0001 | g0231 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG03471 | hp2 | a0003 | c0003 | t0002 | g0213 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG06807 | hp1 | a0005 | c0009 | t0002 | g0037 | AFR | USA | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
HG06807 | hp2 | a0006 | c0006 | t0001 | g0273 | AFR | USA | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18955 | hp1 | a0004 | c0004 | t0001 | g0242 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | USA | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA21309 | hp1 | a0006 | c0006 | t0001 | g0075 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0173 | REF | REF | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0257 | REF | REF | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:56854927
|
T | C | 1 | a0012 | 2 | NA18939.hp2 NA18968.hp2 |
missense_variant | MODERATE | c.26T>C | p.Leu9Ser | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/11 | 131/2367 | 26/1755 | 9/584 | chr1 | 56854927 | ||
chr1:56867631
|
C | T | 2 | a0008a0020 | 5 | HG01346.hp2 HG01358.hp1 HG01496.hp2 others(2): Show |
missense_variant | MODERATE | c.100C>T | p.Pro34Ser | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/11 | 205/2367 | 100/1755 | 34/584 | chr1 | 56867631 | ||
chr1:56867638
|
C | A | 2 | a0007a0019 | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
missense_variant | MODERATE | c.107C>A | p.Ala36Glu | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/11 | 212/2367 | 107/1755 | 36/584 | chr1 | 56867638 | ||
chr1:56874953
|
G | A | 1 | a0013 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.176G>A | p.Arg59Gln | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/11 | 281/2367 | 176/1755 | 59/584 | chr1 | 56874953 | ||
chr1:56875054
|
C | A | 4 | a0002a0005a0009others(1): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
missense_variant | MODERATE | c.277C>A | p.Gln93Lys | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/11 | 382/2367 | 277/1755 | 93/584 | chr1 | 56875054 | ||
chr1:56906790
|
C | T | 2 | a0014a0015 | 2 | HG01243.hp2 HG03098.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1220C>T | p.Thr407Ile | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/11 | 1325/2367 | 1220/1755 | 407/584 | chr1 | 56906790 | ||
chr1:56908105
|
G | A | 3 | a0006a0015a0018 | 11 | HG02622.hp2 HG02630.hp2 HG02895.hp1 others(8): Show |
missense_variant | MODERATE | c.1372G>A | p.Asp458Asn | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/11 | 1477/2367 | 1372/1755 | 458/584 | chr1 | 56908105 | ||
chr1:56912427
|
C | T | 1 | a0017 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1405C>T | p.Arg469Trp | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1510/2367 | 1405/1755 | 469/584 | chr1 | 56912427 | ||
chr1:56912446
|
C | G | 1 | a0016 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1424C>G | p.Pro475Arg | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1529/2367 | 1424/1755 | 475/584 | chr1 | 56912446 | ||
chr1:56912476
|
G | T | 6 | a0003a0005a0007others(3): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
missense_variant | MODERATE | c.1454G>T | p.Arg485Leu | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1559/2367 | 1454/1755 | 485/584 | chr1 | 56912476 | ||
chr1:56917615
|
A | G | 1 | a0011 | 2 | HG00408.hp2 NA19007.hp1 |
missense_variant | MODERATE | c.1654A>G | p.Arg552Gly | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1759/2367 | 1654/1755 | 552/584 | chr1 | 56917615 | ||
chr1:56917622
|
G | A | 1 | a0009 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1661G>A | p.Gly554Asp | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1766/2367 | 1661/1755 | 554/584 | chr1 | 56917622 | ||
chr1:56917642
|
G | C | 7 | a0003a0005a0007others(4): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
missense_variant | MODERATE | c.1681G>C | p.Glu561Gln | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1786/2367 | 1681/1755 | 561/584 | chr1 | 56917642 | ||
chr1:56917685
|
C | T | 3 | a0004a0010a0019 | 20 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(17): Show |
missense_variant | MODERATE | c.1724C>T | p.Pro575Leu | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1829/2367 | 1724/1755 | 575/584 | chr1 | 56917685 | ||
chr1:56917703
|
C | G | 1 | a0013 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1742C>G | p.Thr581Arg | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1847/2367 | 1742/1755 | 581/584 | chr1 | 56917703 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:56867639
|
A | G | 1 | a0001c0023 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.108A>G | p.Ala36Ala | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/11 | 213/2367 | 108/1755 | 36/584 | chr1 | 56867639 | ||
chr1:56881571
|
C | G | 2 | a0007c0007a0019c0015 | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
synonymous_variant | LOW | c.591C>G | p.Leu197Leu | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/11 | 696/2367 | 591/1755 | 197/584 | chr1 | 56881571 | ||
chr1:56885938
|
C | T | 1 | a0001c0010 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.867C>T | p.Phe289Phe | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/11 | 972/2367 | 867/1755 | 289/584 | chr1 | 56885938 | ||
chr1:56912477
|
C | T | 7 | a0003c0003a0005c0005a0005c0009others(4): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
synonymous_variant | LOW | c.1455C>T | p.Arg485Arg | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1560/2367 | 1455/1755 | 485/584 | chr1 | 56912477 | ||
chr1:56912525
|
T | C | 7 | a0003c0003a0005c0005a0005c0009others(4): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
synonymous_variant | LOW | c.1503T>C | p.Pro501Pro | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1608/2367 | 1503/1755 | 501/584 | chr1 | 56912525 | ||
chr1:56912561
|
C | T | 1 | a0001c0018 | 1 | NA19080.hp1 | synonymous_variant | LOW | c.1539C>T | p.Thr513Thr | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1644/2367 | 1539/1755 | 513/584 | chr1 | 56912561 | ||
chr1:56917704
|
G | T | 2 | a0005c0009a0014c0022 | 4 | HG01243.hp2 HG02486.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.1743G>T | p.Thr581Thr | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1848/2367 | 1743/1755 | 581/584 | chr1 | 56917704 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:56854814
|
C | G | 2 | a0007c0007t0004a0019c0015t0007 | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-88C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/11 | 88 | chr1 | 56854814 | |||||
chr1:56917808
|
C | G | 1 | a0002c0002t0006 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 92 | chr1 | 56917808 | |||||
chr1:56917859
|
G | T | 2 | a0001c0001t0005a0017c0020t0005 | 3 | HG02818.hp1 HG03579.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*143G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 143 | chr1 | 56917859 | |||||
chr1:56918010
|
C | T | 8 | a0003c0003t0002a0005c0005t0002a0005c0009t0002others(5): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*294C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 294 | chr1 | 56918010 | |||||
chr1:56918192
|
A | G | 3 | a0001c0001t0003a0001c0001t0005a0017c0020t0005 | 10 | HG02615.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*476A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 476 | chr1 | 56918192 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:56855019
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.77+41A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855019 | ||||||
chr1:56855389
|
C | T | 3 | a0003c0003t0002g0279a0003c0003t0002g0280a0003c0003t0002g0281 | 3 | HG02145.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.77+411C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855389 | ||||||
chr1:56855391
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.77+413T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855391 | ||||||
chr1:56855418
|
T | TAAGAGTG others(311): Show |
1 | a0001c0001t0001g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.77+454_77+455insCG others(316): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56855418 | |||||
chr1:56855488
|
G | A | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+510G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855488 | ||||||
chr1:56855498
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | NA19002.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.77+520A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855498 | ||||||
chr1:56855540
|
T | C | 2 | a0002c0002t0001g0009a0002c0002t0001g0057 | 4 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+562T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855540 | ||||||
chr1:56855550
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 5 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+572G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855550 | ||||||
chr1:56855636
|
GT | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 253 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.77+670delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56855636 | |||||
chr1:56855636
|
GTT | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(11): Show | 23 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.77+669_77+670delTT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56855636 | |||||
chr1:56855703
|
C | T | 1 | a0002c0002t0001g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.77+725C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855703 | ||||||
chr1:56855981
|
C | G | 1 | a0014c0022t0002g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.77+1003C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855981 | ||||||
chr1:56855988
|
G | A | 1 | a0001c0023t0001g0071 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+1010G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855988 | ||||||
chr1:56856017
|
T | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0074others(20): Show | 29 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.77+1039T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856017 | ||||||
chr1:56856037
|
G | T | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+1059G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856037 | ||||||
chr1:56856044
|
G | A | 7 | a0001c0001t0001g0073a0001c0001t0001g0074a0003c0003t0002g0016others(4): Show | 9 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+1066G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856044 | ||||||
chr1:56856132
|
C | T | 1 | a0006c0006t0001g0089 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.77+1154C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856132 | ||||||
chr1:56856170
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.77+1192G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856170 | ||||||
chr1:56856187
|
G | A | 1 | a0002c0002t0001g0090 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.77+1209G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856187 | ||||||
chr1:56856356
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.77+1378A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856356 | ||||||
chr1:56856404
|
C | A | 1 | a0002c0002t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.77+1426C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856404 | ||||||
chr1:56856491
|
C | G | 3 | a0003c0003t0002g0279a0003c0003t0002g0280a0003c0003t0002g0281 | 3 | HG02145.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.77+1513C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856491 | ||||||
chr1:56856557
|
T | C | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+1579T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856557 | ||||||
chr1:56856644
|
A | G | 13 | a0001c0001t0001g0050a0001c0001t0001g0070a0001c0001t0001g0217others(10): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.77+1666A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856644 | ||||||
chr1:56856793
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.77+1815A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856793 | ||||||
chr1:56856861
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0278others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+1883G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856861 | ||||||
chr1:56856914
|
T | G | 1 | a0002c0002t0001g0092 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.77+1936T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856914 | ||||||
chr1:56857057
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.77+2079G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857057 | ||||||
chr1:56857229
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.77+2251A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857229 | ||||||
chr1:56857303
|
T | TAC | 105 | a0001c0001t0001g0038a0001c0001t0001g0073a0001c0001t0001g0074others(102): Show | 132 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.77+2351_77+2352dup others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | |||||
chr1:56857303
|
T | TACAC | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(58): Show | 90 | HG00544.hp2 HG00609.hp2 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.77+2349_77+2352dup others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | |||||
chr1:56857303
|
T | TACACAC | 21 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0051others(18): Show | 28 | HG00408.hp2 HG00621.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.77+2347_77+2352dup others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | |||||
chr1:56857303
|
T | TACACACA others(1): Show |
6 | a0001c0001t0001g0018a0001c0001t0001g0095a0007c0007t0004g0054others(3): Show | 7 | HG00323.hp1 HG01243.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+2345_77+2352dup others(8): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | |||||
chr1:56857303
|
T | TACACACA others(3): Show |
2 | a0003c0003t0002g0094a0007c0007t0004g0052 | 2 | HG01943.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.77+2343_77+2352dup others(10): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | |||||
chr1:56857442
|
A | T | 2 | a0002c0002t0001g0211a0002c0002t0001g0212 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.77+2464A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857442 | ||||||
chr1:56857506
|
T | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.77+2528T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857506 | ||||||
chr1:56857691
|
G | A | 89 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0143others(86): Show | 112 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.77+2713G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857691 | ||||||
chr1:56857880
|
T | G | 13 | a0001c0001t0001g0050a0001c0001t0001g0070a0001c0001t0001g0217others(10): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.77+2902T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857880 | ||||||
chr1:56858022
|
G | T | 1 | a0002c0002t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.77+3044G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858022 | ||||||
chr1:56858090
|
C | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 282 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(279): Show |
intron_variant | MODIFIER | c.77+3112C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858090 | ||||||
chr1:56858417
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.77+3439T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858417 | ||||||
chr1:56858636
|
G | A | 2 | a0014c0022t0002g0220a0015c0021t0001g0072 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.77+3658G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858636 | ||||||
chr1:56858749
|
C | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 282 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(279): Show |
intron_variant | MODIFIER | c.77+3771C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858749 | ||||||
chr1:56858785
|
C | A | 2 | a0001c0001t0001g0197a0003c0003t0002g0198 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.77+3807C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858785 | ||||||
chr1:56858813
|
T | C | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0003c0003t0002g0016 | 4 | HG02280.hp2 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+3835T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858813 | ||||||
chr1:56858839
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 285 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(282): Show |
intron_variant | MODIFIER | c.77+3861A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858839 | ||||||
chr1:56859067
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0062a0001c0001t0001g0063 | 4 | HG02071.hp2 HG02135.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+4089G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859067 | ||||||
chr1:56859222
|
G | A | 1 | a0002c0002t0001g0138 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.77+4244G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859222 | ||||||
chr1:56859224
|
A | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(20): Show | 32 | HG00408.hp2 HG01168.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.77+4246A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859224 | ||||||
chr1:56859586
|
T | A | 2 | a0001c0001t0001g0197a0003c0003t0002g0198 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.77+4608T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859586 | ||||||
chr1:56859715
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.77+4737C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859715 | ||||||
chr1:56859761
|
A | AC | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 285 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(282): Show |
intron_variant | MODIFIER | c.77+4783_77+4784ins others(1): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859761 | ||||||
chr1:56859791
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.77+4813G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859791 | ||||||
chr1:56859904
|
A | T | 1 | a0004c0004t0001g0039 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.77+4926A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859904 | ||||||
chr1:56860018
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.77+5040G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860018 | ||||||
chr1:56860074
|
T | A | 102 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0143others(99): Show | 126 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.77+5096T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860074 | ||||||
chr1:56860182
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 251 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.77+5204A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860182 | ||||||
chr1:56860208
|
G | A | 1 | a0002c0002t0001g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.77+5230G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860208 | ||||||
chr1:56860209
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.77+5231C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860209 | ||||||
chr1:56860313
|
G | A | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+5335G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860313 | ||||||
chr1:56860400
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0003g0017a0001c0001t0003g0076others(1): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+5422A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860400 | ||||||
chr1:56860451
|
A | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.77+5473A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860451 | ||||||
chr1:56860491
|
T | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0230 | 3 | HG00735.hp1 HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.77+5513T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860491 | ||||||
chr1:56860562
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(11): Show | 23 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.77+5584G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860562 | ||||||
chr1:56860750
|
T | C | 1 | a0016c0019t0001g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.77+5772T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860750 | ||||||
chr1:56860761
|
G | A | 3 | a0002c0002t0001g0140a0002c0002t0001g0141a0002c0002t0001g0142 | 3 | HG02738.hp1 HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.77+5783G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860761 | ||||||
chr1:56860779
|
C | T | 1 | a0004c0004t0001g0271 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.77+5801C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860779 | ||||||
chr1:56860877
|
A | G | 1 | a0016c0019t0001g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.77+5899A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860877 | ||||||
chr1:56861027
|
G | A | 1 | a0003c0003t0002g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.77+6049G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861027 | ||||||
chr1:56861160
|
T | A | 2 | a0001c0001t0001g0197a0003c0003t0002g0198 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.77+6182T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861160 | ||||||
chr1:56861264
|
A | G | 14 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0083others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+6286A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861264 | ||||||
chr1:56861338
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(12): Show | 24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.78-6271G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861338 | ||||||
chr1:56861462
|
CA | C | 2 | a0001c0001t0001g0038a0003c0003t0002g0213 | 3 | HG02572.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.78-6146delA | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861462 | ||||||
chr1:56861498
|
G | T | 1 | a0001c0023t0001g0071 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.78-6111G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861498 | ||||||
chr1:56861526
|
T | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(11): Show | 23 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.78-6083T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861526 | ||||||
chr1:56861547
|
C | T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78-6062C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861547 | ||||||
chr1:56861570
|
A | T | 1 | a0017c0020t0005g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.78-6039A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861570 | ||||||
chr1:56861611
|
T | A | 2 | a0014c0022t0002g0220a0015c0021t0001g0072 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.78-5998T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861611 | ||||||
chr1:56861698
|
T | C | 15 | a0001c0001t0001g0050a0001c0001t0001g0078a0001c0001t0001g0080others(12): Show | 16 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.78-5911T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861698 | ||||||
chr1:56861792
|
T | C | 4 | a0001c0001t0001g0070a0001c0001t0005g0216a0003c0003t0002g0040others(1): Show | 5 | HG03490.hp1 HG03492.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-5817T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861792 | ||||||
chr1:56862122
|
C | T | 1 | a0004c0004t0001g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.78-5487C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862122 | ||||||
chr1:56862197
|
A | G | 7 | a0001c0001t0001g0038a0001c0001t0001g0229a0001c0001t0001g0267others(4): Show | 8 | HG02572.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.78-5412A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862197 | ||||||
chr1:56862310
|
C | T | 93 | a0001c0001t0001g0195a0002c0002t0001g0001a0002c0002t0001g0009others(90): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.78-5299C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862310 | ||||||
chr1:56862321
|
A | G | 1 | a0002c0002t0001g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.78-5288A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862321 | ||||||
chr1:56862449
|
C | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 236 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.78-5160C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862449 | ||||||
chr1:56862622
|
C | T | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-4987C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862622 | ||||||
chr1:56863029
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.78-4580G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863029 | ||||||
chr1:56863057
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.78-4552C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863057 | ||||||
chr1:56863092
|
G | C | 1 | a0001c0001t0001g0100 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.78-4517G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863092 | ||||||
chr1:56863115
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.78-4494A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863115 | ||||||
chr1:56863192
|
G | T | 1 | a0006c0006t0001g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.78-4417G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863192 | ||||||
chr1:56863253
|
T | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 238 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.78-4356T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863253 | ||||||
chr1:56863729
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.78-3880C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863729 | ||||||
chr1:56863831
|
TC | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(12): Show | 24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.78-3775delC | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56863831 | |||||
chr1:56863831
|
TCCCTCTC others(18): Show |
T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78-3768_78-3744del others(25): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56863831 | |||||
chr1:56863885
|
CCCTT | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG00558.hp1 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-3707_78-3704del others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56863885 | |||||
chr1:56863886
|
C | T | 1 | a0002c0002t0001g0193 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.78-3723C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863886 | ||||||
chr1:56864044
|
G | C | 1 | a0001c0010t0001g0231 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-3565G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864044 | ||||||
chr1:56864129
|
G | A | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-3480G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864129 | ||||||
chr1:56864264
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.78-3345G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864264 | ||||||
chr1:56864361
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.78-3248C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864361 | ||||||
chr1:56864376
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.78-3233A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864376 | ||||||
chr1:56864389
|
G | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(20): Show | 32 | HG00408.hp2 HG01168.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.78-3220G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864389 | ||||||
chr1:56864443
|
T | A | 6 | a0001c0001t0001g0229a0001c0001t0001g0267a0001c0001t0001g0268others(3): Show | 6 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-3166T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864443 | ||||||
chr1:56864578
|
G | A | 1 | a0002c0002t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.78-3031G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864578 | ||||||
chr1:56864739
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.78-2870G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864739 | ||||||
chr1:56864740
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.78-2869A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864740 | ||||||
chr1:56865052
|
C | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(57): Show | 85 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.78-2557C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865052 | ||||||
chr1:56865068
|
T | C | 5 | a0001c0001t0001g0218a0001c0001t0001g0274a0003c0003t0002g0279others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-2541T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865068 | ||||||
chr1:56865296
|
C | A | 1 | a0005c0005t0002g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.78-2313C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865296 | ||||||
chr1:56865353
|
T | G | 29 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(26): Show | 37 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.78-2256T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865353 | ||||||
chr1:56865372
|
C | T | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.78-2237C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865372 | ||||||
chr1:56865409
|
G | T | 93 | a0001c0001t0001g0195a0002c0002t0001g0001a0002c0002t0001g0009others(90): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.78-2200G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865409 | ||||||
chr1:56865454
|
G | T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78-2155G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865454 | ||||||
chr1:56865830
|
T | C | 6 | a0001c0001t0001g0229a0001c0001t0001g0267a0001c0001t0001g0268others(3): Show | 6 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-1779T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865830 | ||||||
chr1:56865873
|
G | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.78-1736G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865873 | ||||||
chr1:56866070
|
T | A | 5 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0147others(2): Show | 5 | HG02273.hp2 NA18989.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-1539T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866070 | ||||||
chr1:56866148
|
T | C | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-1461T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866148 | ||||||
chr1:56866221
|
A | C | 1 | a0001c0001t0003g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.78-1388A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866221 | ||||||
chr1:56866251
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.78-1358A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866251 | ||||||
chr1:56866598
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.78-1011G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866598 | ||||||
chr1:56866632
|
C | T | 1 | a0005c0005t0002g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.78-977C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866632 | ||||||
chr1:56866716
|
A | G | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78-893A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866716 | ||||||
chr1:56866762
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.78-847G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866762 | ||||||
chr1:56866812
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.78-797A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866812 | ||||||
chr1:56866816
|
G | T | 2 | a0003c0003t0002g0219a0016c0019t0001g0209 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.78-793G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866816 | ||||||
chr1:56866826
|
G | A | 1 | a0008c0008t0001g0248 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.78-783G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866826 | ||||||
chr1:56866831
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.78-778G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866831 | ||||||
chr1:56866906
|
A | T | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.78-703A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866906 | ||||||
chr1:56866945
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0136 | 5 | HG00544.hp2 NA18957.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-664C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866945 | ||||||
chr1:56867049
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0226 | 2 | NA18956.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.78-560A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867049 | ||||||
chr1:56867084
|
T | C | 35 | a0001c0001t0001g0107a0002c0002t0001g0001a0002c0002t0001g0025others(32): Show | 47 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.78-525T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867084 | ||||||
chr1:56867130
|
T | G | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.78-479T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867130 | ||||||
chr1:56867182
|
A | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(20): Show | 32 | HG00408.hp2 HG01168.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.78-427A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867182 | ||||||
chr1:56867197
|
A | G | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-412A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867197 | ||||||
chr1:56867206
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78-403G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867206 | ||||||
chr1:56867710
|
A | G | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | splice_region_variant&intron_variant | LOW | c.171+8A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867710 | ||||||
chr1:56867761
|
C | T | 6 | a0001c0001t0001g0229a0001c0001t0001g0267a0001c0001t0001g0268others(3): Show | 6 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+59C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867761 | ||||||
chr1:56867810
|
G | T | 13 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0083others(10): Show | 13 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.171+108G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867810 | ||||||
chr1:56867870
|
C | A | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.171+168C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867870 | ||||||
chr1:56867942
|
A | G | 1 | a0002c0002t0001g0166 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.171+240A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867942 | ||||||
chr1:56867948
|
T | C | 1 | a0002c0002t0001g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.171+246T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867948 | ||||||
chr1:56868083
|
G | A | 1 | a0005c0005t0002g0167 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.171+381G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868083 | ||||||
chr1:56868086
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 248 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.171+384A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868086 | ||||||
chr1:56868412
|
C | T | 2 | a0002c0002t0001g0138a0002c0002t0001g0191 | 2 | HG02165.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.171+710C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868412 | ||||||
chr1:56868482
|
A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 236 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.171+780A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868482 | ||||||
chr1:56868547
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.171+845G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868547 | ||||||
chr1:56868595
|
G | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(59): Show | 87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+893G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868595 | ||||||
chr1:56868735
|
A | G | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171+1033A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868735 | ||||||
chr1:56868738
|
A | C | 2 | a0003c0003t0002g0219a0016c0019t0001g0209 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.171+1036A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868738 | ||||||
chr1:56868773
|
C | T | 2 | a0003c0003t0002g0219a0016c0019t0001g0209 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.171+1071C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868773 | ||||||
chr1:56868883
|
T | C | 1 | a0002c0002t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.171+1181T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868883 | ||||||
chr1:56869046
|
T | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.171+1344T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869046 | ||||||
chr1:56869145
|
T | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(59): Show | 87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+1443T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869145 | ||||||
chr1:56869201
|
C | T | 6 | a0001c0001t0001g0049a0008c0008t0001g0248a0008c0008t0001g0259others(3): Show | 7 | HG01346.hp2 HG01358.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+1499C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869201 | ||||||
chr1:56869318
|
G | T | 1 | a0001c0001t0001g0277 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.171+1616G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869318 | ||||||
chr1:56869445
|
T | C | 1 | a0002c0002t0001g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.171+1743T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869445 | ||||||
chr1:56869475
|
A | G | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171+1773A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869475 | ||||||
chr1:56869520
|
G | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(268): Show | 348 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.171+1818G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869520 | ||||||
chr1:56869533
|
C | T | 49 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0050others(46): Show | 58 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(55): Show |
intron_variant | MODIFIER | c.171+1831C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869533 | ||||||
chr1:56869634
|
G | A | 92 | a0002c0002t0001g0001a0002c0002t0001g0009a0002c0002t0001g0025others(89): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.171+1932G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869634 | ||||||
chr1:56869686
|
G | C | 1 | a0006c0006t0001g0089 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.171+1984G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869686 | ||||||
chr1:56869803
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(59): Show | 87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+2101C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869803 | ||||||
chr1:56869809
|
C | T | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171+2107C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869809 | ||||||
chr1:56869849
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0278others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+2147C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869849 | ||||||
chr1:56869884
|
A | G | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.171+2182A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869884 | ||||||
chr1:56869908
|
G | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(59): Show | 87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+2206G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869908 | ||||||
chr1:56870078
|
T | G | 2 | a0002c0002t0001g0150a0002c0002t0001g0151 | 2 | NA18969.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.171+2376T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870078 | ||||||
chr1:56870085
|
G | A | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.171+2383G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870085 | ||||||
chr1:56870245
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.171+2543G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870245 | ||||||
chr1:56870367
|
G | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 95 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.171+2665G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870367 | ||||||
chr1:56870405
|
G | A | 4 | a0001c0001t0001g0038a0001c0010t0001g0231a0001c0010t0001g0263others(1): Show | 5 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+2703G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870405 | ||||||
chr1:56870581
|
G | T | 92 | a0002c0002t0001g0001a0002c0002t0001g0009a0002c0002t0001g0025others(89): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.171+2879G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870581 | ||||||
chr1:56870670
|
C | T | 1 | a0005c0005t0002g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.171+2968C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870670 | ||||||
chr1:56870681
|
T | TAAATTAA others(6): Show |
1 | a0001c0001t0001g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.171+2979_171+2980i others(15): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870681 | ||||||
chr1:56870681
|
T | TAAATTAA others(16): Show |
5 | a0001c0001t0001g0109a0001c0001t0001g0217a0003c0003t0002g0279others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+2979_171+2980i others(25): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870681 | ||||||
chr1:56870681
|
T | TAAATTAA others(21): Show |
4 | a0001c0001t0001g0218a0001c0001t0005g0216a0003c0003t0002g0040others(1): Show | 5 | HG03139.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+2979_171+2980i others(30): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870681 | ||||||
chr1:56870681
|
T | TAAATTAA others(26): Show |
1 | a0001c0001t0001g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.171+2979_171+2980i others(35): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870681 | ||||||
chr1:56870683
|
T | TAAA | 11 | a0001c0001t0001g0070a0001c0001t0001g0109a0001c0001t0001g0217others(8): Show | 12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2981_171+2982i others(5): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870683 | ||||||
chr1:56870685
|
C | T | 11 | a0001c0001t0001g0070a0001c0001t0001g0109a0001c0001t0001g0217others(8): Show | 12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2983C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870685 | ||||||
chr1:56870686
|
G | A | 11 | a0001c0001t0001g0070a0001c0001t0001g0109a0001c0001t0001g0217others(8): Show | 12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2984G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870686 | ||||||
chr1:56870687
|
T | A | 11 | a0001c0001t0001g0070a0001c0001t0001g0109a0001c0001t0001g0217others(8): Show | 12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2985T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870687 | ||||||
chr1:56870725
|
T | C | 1 | a0002c0002t0001g0170 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.171+3023T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870725 | ||||||
chr1:56870849
|
A | T | 1 | a0001c0001t0001g0134 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.171+3147A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870849 | ||||||
chr1:56870887
|
G | T | 3 | a0002c0002t0001g0140a0002c0002t0001g0141a0002c0002t0001g0142 | 3 | HG02738.hp1 HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.171+3185G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870887 | ||||||
chr1:56871015
|
C | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0115 | 3 | NA18961.hp2 NA18965.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.171+3313C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871015 | ||||||
chr1:56871038
|
C | T | 1 | a0004c0004t0001g0247 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.171+3336C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871038 | ||||||
chr1:56871070
|
A | G | 1 | a0001c0001t0001g0024 | 2 | NA18969.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.171+3368A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871070 | ||||||
chr1:56871102
|
G | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(59): Show | 87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+3400G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871102 | ||||||
chr1:56871157
|
G | A | 1 | a0002c0002t0001g0171 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.171+3455G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871157 | ||||||
chr1:56871197
|
G | A | 1 | a0003c0003t0002g0198 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.171+3495G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871197 | ||||||
chr1:56871317
|
C | T | 1 | a0001c0001t0001g0024 | 2 | NA18969.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.171+3615C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871317 | ||||||
chr1:56871462
|
G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 92 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.172-3487G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871462 | ||||||
chr1:56871877
|
T | A | 1 | a0017c0020t0005g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.172-3072T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871877 | ||||||
chr1:56871924
|
T | C | 2 | a0001c0001t0005g0216a0006c0006t0001g0215 | 2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-3025T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871924 | ||||||
chr1:56872087
|
T | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.172-2862T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872087 | ||||||
chr1:56872284
|
C | T | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.172-2665C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872284 | ||||||
chr1:56872357
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.172-2592G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872357 | ||||||
chr1:56872380
|
T | C | 1 | a0002c0002t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.172-2569T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872380 | ||||||
chr1:56872409
|
A | G | 1 | a0002c0002t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.172-2540A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872409 | ||||||
chr1:56872448
|
A | T | 1 | a0001c0001t0001g0133 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.172-2501A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872448 | ||||||
chr1:56872549
|
T | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-2400T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872549 | ||||||
chr1:56872559
|
G | A | 2 | a0004c0004t0001g0232a0004c0004t0001g0233 | 2 | HG00280.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.172-2390G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872559 | ||||||
chr1:56872905
|
A | AAAAG | 11 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0058others(8): Show | 13 | HG00423.hp1 HG00735.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-2032_172-2029d others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 56872905 | |||||
chr1:56872905
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.172-2044A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872905 | ||||||
chr1:56872972
|
G | A | 2 | a0001c0001t0005g0216a0006c0006t0001g0215 | 2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-1977G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872972 | ||||||
chr1:56873055
|
A | G | 4 | a0001c0001t0001g0274a0003c0003t0002g0279a0003c0003t0002g0280others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1894A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873055 | ||||||
chr1:56873212
|
A | G | 6 | a0002c0002t0001g0145a0002c0002t0001g0146a0002c0002t0001g0147others(3): Show | 6 | HG00558.hp1 HG02273.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1737A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873212 | ||||||
chr1:56873252
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.172-1697T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873252 | ||||||
chr1:56873320
|
C | T | 2 | a0014c0022t0002g0220a0015c0021t0001g0072 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.172-1629C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873320 | ||||||
chr1:56873361
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 179 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.172-1588A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873361 | ||||||
chr1:56873458
|
C | G | 1 | a0002c0002t0001g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.172-1491C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873458 | ||||||
chr1:56873487
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.172-1462T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873487 | ||||||
chr1:56873514
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0282 | 2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.172-1435G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873514 | ||||||
chr1:56873612
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0134 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.172-1337C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873612 | ||||||
chr1:56873614
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.172-1335C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873614 | ||||||
chr1:56873774
|
A | G | 11 | a0001c0001t0001g0070a0001c0001t0001g0109a0001c0001t0001g0217others(8): Show | 12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-1175A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873774 | ||||||
chr1:56873907
|
T | C | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.172-1042T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873907 | ||||||
chr1:56873979
|
C | A | 2 | a0001c0001t0001g0093a0004c0004t0001g0039 | 3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.172-970C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873979 | ||||||
chr1:56874047
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(2): Show | 10 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-902C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874047 | ||||||
chr1:56874186
|
A | G | 4 | a0001c0001t0001g0070a0001c0001t0005g0216a0003c0003t0002g0040others(1): Show | 5 | HG03490.hp1 HG03492.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-763A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874186 | ||||||
chr1:56874299
|
C | G | 5 | a0001c0001t0001g0229a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG02886.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-650C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874299 | ||||||
chr1:56874468
|
G | A | 1 | a0016c0019t0001g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.172-481G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874468 | ||||||
chr1:56874557
|
G | A | 1 | a0005c0005t0002g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.172-392G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874557 | ||||||
chr1:56874610
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.172-339G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874610 | ||||||
chr1:56874640
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.172-309T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874640 | ||||||
chr1:56874660
|
G | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0004c0004t0001g0245others(2): Show | 8 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-289G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874660 | ||||||
chr1:56874675
|
G | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(12): Show | 24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.172-274G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874675 | ||||||
chr1:56874699
|
C | G | 2 | a0003c0003t0002g0219a0016c0019t0001g0209 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.172-250C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874699 | ||||||
chr1:56874708
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.172-241A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874708 | ||||||
chr1:56874802
|
A | T | 24 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(21): Show | 32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.172-147A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874802 | ||||||
chr1:56874844
|
C | A | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.172-105C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874844 | ||||||
chr1:56874873
|
G | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG01168.hp2 HG01433.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-76G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874873 | ||||||
chr1:56875101
|
G | A | 5 | a0001c0001t0001g0038a0001c0010t0001g0231a0001c0010t0001g0263others(2): Show | 6 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.316+8G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875101 | ||||||
chr1:56875187
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+94G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875187 | ||||||
chr1:56875199
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.316+106G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875199 | ||||||
chr1:56875233
|
A | G | 1 | a0003c0003t0002g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.316+140A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875233 | ||||||
chr1:56875367
|
A | G | 1 | a0004c0004t0001g0271 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.316+274A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875367 | ||||||
chr1:56875499
|
A | T | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+406A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875499 | ||||||
chr1:56875651
|
T | C | 1 | a0002c0002t0001g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.317-411T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875651 | ||||||
chr1:56875731
|
A | G | 1 | a0007c0007t0004g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.317-331A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875731 | ||||||
chr1:56875952
|
A | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-110A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875952 | ||||||
chr1:56875972
|
A | T | 2 | a0001c0001t0001g0093a0004c0004t0001g0039 | 3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.317-90A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875972 | ||||||
chr1:56876036
|
G | C | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.317-26G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56876036 | ||||||
chr1:56876220
|
G | T | 1 | a0002c0002t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.464+11G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876220 | ||||||
chr1:56876290
|
G | C | 1 | a0002c0002t0001g0138 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.464+81G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876290 | ||||||
chr1:56876445
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.464+236C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876445 | ||||||
chr1:56876505
|
C | T | 1 | a0002c0002t0001g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.464+296C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876505 | ||||||
chr1:56876523
|
T | C | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+314T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876523 | ||||||
chr1:56876749
|
C | A | 24 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(21): Show | 32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.464+540C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876749 | ||||||
chr1:56876752
|
T | G | 1 | a0002c0002t0001g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.464+543T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876752 | ||||||
chr1:56876948
|
C | T | 83 | a0002c0002t0001g0001a0002c0002t0001g0009a0002c0002t0001g0025others(80): Show | 105 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.464+739C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876948 | ||||||
chr1:56877025
|
T | C | 1 | a0018c0017t0002g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.464+816T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877025 | ||||||
chr1:56877090
|
T | G | 2 | a0002c0002t0001g0110a0002c0002t0001g0111 | 2 | NA18979.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.464+881T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877090 | ||||||
chr1:56877093
|
A | C | 3 | a0003c0003t0002g0279a0003c0003t0002g0280a0003c0003t0002g0281 | 3 | HG02145.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464+884A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877093 | ||||||
chr1:56877155
|
C | A | 1 | a0007c0007t0004g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.464+946C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877155 | ||||||
chr1:56877160
|
A | G | 2 | a0001c0001t0001g0251a0006c0006t0001g0047 | 3 | HG02895.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.464+951A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877160 | ||||||
chr1:56877296
|
G | T | 1 | a0001c0001t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.464+1087G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877296 | ||||||
chr1:56877332
|
C | T | 2 | a0003c0003t0002g0219a0016c0019t0001g0209 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.464+1123C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877332 | ||||||
chr1:56877583
|
T | G | 92 | a0002c0002t0001g0001a0002c0002t0001g0009a0002c0002t0001g0025others(89): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.464+1374T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877583 | ||||||
chr1:56877643
|
C | T | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+1434C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877643 | ||||||
chr1:56877673
|
G | A | 1 | a0003c0003t0002g0252 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.464+1464G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877673 | ||||||
chr1:56877849
|
A | G | 92 | a0002c0002t0001g0001a0002c0002t0001g0009a0002c0002t0001g0025others(89): Show | 115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.464+1640A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877849 | ||||||
chr1:56877856
|
C | A | 1 | a0001c0001t0001g0256 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.464+1647C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877856 | ||||||
chr1:56877918
|
A | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(2): Show | 10 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.464+1709A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877918 | ||||||
chr1:56878049
|
C | T | 21 | a0002c0002t0001g0028a0002c0002t0001g0033a0002c0002t0001g0034others(18): Show | 25 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.464+1840C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878049 | ||||||
chr1:56878067
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.464+1858G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878067 | ||||||
chr1:56878097
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 179 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.464+1888T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878097 | ||||||
chr1:56878172
|
T | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0050others(11): Show | 22 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.464+1963T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878172 | ||||||
chr1:56878178
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.464+1969C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878178 | ||||||
chr1:56878224
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.464+2015C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878224 | ||||||
chr1:56878353
|
G | A | 2 | a0001c0001t0001g0093a0004c0004t0001g0039 | 3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.464+2144G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878353 | ||||||
chr1:56878371
|
T | C | 4 | a0001c0001t0001g0070a0001c0001t0005g0216a0003c0003t0002g0040others(1): Show | 5 | HG03490.hp1 HG03492.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+2162T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878371 | ||||||
chr1:56878489
|
G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(80): Show | 109 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.464+2280G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878489 | ||||||
chr1:56878577
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.464+2368C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878577 | ||||||
chr1:56878641
|
A | G | 8 | a0001c0001t0001g0073a0001c0001t0001g0074a0003c0003t0002g0016others(5): Show | 10 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.464+2432A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878641 | ||||||
chr1:56878702
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(80): Show | 109 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.464+2493T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878702 | ||||||
chr1:56878717
|
A | G | 1 | a0001c0010t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.464+2508A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878717 | ||||||
chr1:56878738
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.464+2529G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878738 | ||||||
chr1:56879053
|
C | T | 1 | a0005c0005t0002g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.465-2392C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879053 | ||||||
chr1:56879137
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.465-2308G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879137 | ||||||
chr1:56879178
|
A | T | 2 | a0003c0003t0002g0219a0016c0019t0001g0209 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.465-2267A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879178 | ||||||
chr1:56879320
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.465-2125C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879320 | ||||||
chr1:56879822
|
A | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.465-1623A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879822 | ||||||
chr1:56879941
|
G | A | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.465-1504G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879941 | ||||||
chr1:56880235
|
T | C | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.465-1210T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880235 | ||||||
chr1:56880267
|
A | T | 1 | a0003c0003t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465-1178A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880267 | ||||||
chr1:56880439
|
GTAT | G | 13 | a0002c0002t0001g0033a0002c0002t0001g0034a0002c0002t0001g0172others(10): Show | 14 | HG00423.hp2 HG02015.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.465-999_465-997del others(3): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 56880439 | |||||
chr1:56880462
|
A | C | 1 | a0002c0002t0001g0192 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.465-983A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880462 | ||||||
chr1:56880580
|
T | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0282 | 2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.465-865T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880580 | ||||||
chr1:56880741
|
C | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.465-704C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880741 | ||||||
chr1:56880867
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0065 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.465-578G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880867 | ||||||
chr1:56881161
|
A | G | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.465-284A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56881161 | ||||||
chr1:56881317
|
C | T | 1 | a0002c0002t0001g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.465-128C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56881317 | ||||||
chr1:56881357
|
A | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(46): Show | 66 | HG00408.hp2 HG01109.hp2 HG01243.hp2 others(63): Show |
intron_variant | MODIFIER | c.465-88A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56881357 | ||||||
chr1:56881650
|
G | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(50): Show | 70 | HG00408.hp2 HG01109.hp2 HG01243.hp2 others(67): Show |
intron_variant | MODIFIER | c.654+16G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56881650 | ||||||
chr1:56881814
|
A | T | 1 | a0008c0008t0001g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.654+180A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56881814 | ||||||
chr1:56882036
|
A | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(12): Show | 24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.654+402A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882036 | ||||||
chr1:56882061
|
A | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0050others(11): Show | 22 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.654+427A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882061 | ||||||
chr1:56882194
|
T | C | 1 | a0004c0004t0001g0039 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.654+560T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882194 | ||||||
chr1:56882266
|
A | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 294 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.654+632A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882266 | ||||||
chr1:56882293
|
C | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.654+659C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882293 | ||||||
chr1:56882524
|
TAGA | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0278a0003c0003t0002g0223 | 3 | HG02280.hp1 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.654+897_654+899del others(3): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56882524 | |||||
chr1:56882561
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.655-920A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882561 | ||||||
chr1:56882621
|
G | T | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.655-860G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882621 | ||||||
chr1:56882650
|
C | T | 29 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(26): Show | 37 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.655-831C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882650 | ||||||
chr1:56882727
|
C | T | 1 | a0015c0021t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.655-754C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882727 | ||||||
chr1:56882754
|
C | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0046a0004c0004t0001g0245 | 6 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.655-727C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882754 | ||||||
chr1:56882763
|
C | T | 24 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(21): Show | 32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.655-718C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882763 | ||||||
chr1:56882842
|
A | T | 1 | a0001c0001t0001g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.655-639A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882842 | ||||||
chr1:56882978
|
A | ACAAGGCC others(17): Show |
4 | a0001c0001t0001g0267a0001c0001t0001g0268a0003c0003t0002g0228others(1): Show | 4 | HG02886.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-498_655-475dup others(24): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56882978 | |||||
chr1:56883223
|
C | CTG | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(63): Show | 91 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.655-235_655-234dup others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56883223 | |||||
chr1:56883223
|
C | CTGTG | 78 | a0001c0001t0001g0195a0002c0002t0001g0001a0002c0002t0001g0009others(75): Show | 99 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.655-237_655-234dup others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56883223 | |||||
chr1:56883223
|
C | CTGTGTG | 6 | a0002c0002t0001g0028a0002c0002t0001g0177a0002c0002t0001g0178others(3): Show | 7 | HG00738.hp1 HG01106.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-239_655-234dup others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56883223 | |||||
chr1:56883223
|
CTG | C | 26 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0096others(23): Show | 27 | HG01168.hp2 HG01192.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.655-235_655-234del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56883223 | |||||
chr1:56883297
|
T | G | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-184T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56883297 | ||||||
chr1:56883441
|
C | G | 4 | a0001c0001t0001g0088a0001c0010t0001g0231a0001c0010t0001g0263others(1): Show | 4 | HG02559.hp1 HG02615.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-40C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56883441 | ||||||
chr1:56883445
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.655-36G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56883445 | ||||||
chr1:56883707
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.855+26C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883707 | ||||||
chr1:56883734
|
A | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(69): Show | 98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.855+53A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883734 | ||||||
chr1:56883735
|
C | T | 2 | a0012c0011t0001g0243a0012c0011t0001g0244 | 2 | NA18939.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.855+54C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883735 | ||||||
chr1:56883791
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(69): Show | 98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.855+110T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883791 | ||||||
chr1:56883903
|
T | C | 1 | a0002c0002t0001g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.855+222T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883903 | ||||||
chr1:56883910
|
GC | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.855+237delC | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56883910 | |||||
chr1:56883941
|
T | C | 93 | a0001c0001t0001g0195a0002c0002t0001g0001a0002c0002t0001g0009others(90): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.855+260T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883941 | ||||||
chr1:56884061
|
G | A | 1 | a0005c0005t0002g0167 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.855+380G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884061 | ||||||
chr1:56884067
|
T | TA | 7 | a0001c0001t0001g0088a0001c0001t0001g0119a0001c0001t0001g0135others(4): Show | 7 | HG02698.hp1 HG03017.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+405dupA | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56884067 | |||||
chr1:56884067
|
TA | T | 51 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0061others(48): Show | 54 | HG00323.hp1 HG00673.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.855+405delA | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56884067 | |||||
chr1:56884067
|
TAA | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0064others(6): Show | 17 | HG00408.hp2 HG02015.hp1 HG02922.hp2 others(14): Show |
intron_variant | MODIFIER | c.855+404_855+405del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56884067 | |||||
chr1:56884236
|
G | A | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+555G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884236 | ||||||
chr1:56884434
|
T | G | 1 | a0003c0003t0002g0252 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.855+753T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884434 | ||||||
chr1:56884482
|
T | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(12): Show | 24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.855+801T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884482 | ||||||
chr1:56884832
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-1095G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884832 | ||||||
chr1:56884950
|
T | C | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.856-977T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884950 | ||||||
chr1:56885062
|
GAGA | G | 93 | a0001c0001t0001g0195a0002c0002t0001g0001a0002c0002t0001g0009others(90): Show | 116 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.856-860_856-858del others(3): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885062 | |||||
chr1:56885070
|
C | A | 14 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0083others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.856-857C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885070 | ||||||
chr1:56885149
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.856-778G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885149 | ||||||
chr1:56885242
|
G | T | 2 | a0001c0001t0001g0093a0004c0004t0001g0039 | 3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.856-685G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885242 | ||||||
chr1:56885269
|
T | TATAAATA others(35): Show |
1 | a0001c0001t0001g0253 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.856-647_856-606dup others(42): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885269 | |||||
chr1:56885286
|
A | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(69): Show | 98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.856-641A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885286 | ||||||
chr1:56885303
|
TATATTTA others(5): Show |
T | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-619_856-608del others(12): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885303 | |||||
chr1:56885311
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.856-616C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885311 | ||||||
chr1:56885312
|
A | G | 12 | a0001c0001t0001g0070a0001c0001t0001g0109a0001c0001t0001g0217others(9): Show | 13 | HG01123.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.856-615A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885312 | ||||||
chr1:56885312
|
ATAAATAT others(7): Show |
A | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-605_856-592del others(14): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885312 | |||||
chr1:56885315
|
A | AAT | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 150 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.856-607_856-606dup others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | |||||
chr1:56885315
|
A | AATATATA others(81): Show |
1 | a0001c0001t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-606_856-605ins others(88): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | |||||
chr1:56885315
|
A | AATATATA others(21): Show |
9 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(6): Show | 9 | HG01109.hp2 HG02109.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-606_856-605ins others(28): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | |||||
chr1:56885315
|
A | AATATATA others(47): Show |
1 | a0001c0001t0001g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.856-606_856-605ins others(54): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | |||||
chr1:56885315
|
A | AATATATA others(73): Show |
1 | a0018c0017t0002g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.856-606_856-605ins others(80): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | |||||
chr1:56885315
|
A | AATATATA others(233): Show |
1 | a0001c0001t0001g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.856-606_856-605ins others(240): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | |||||
chr1:56885316
|
A | ATATATAT others(101): Show |
1 | a0001c0001t0001g0078 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856-606_856-605ins others(108): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885316 | |||||
chr1:56885316
|
A | ATATATAT others(17): Show |
3 | a0003c0003t0002g0041a0006c0006t0001g0075a0017c0020t0005g0270 | 4 | HG01891.hp1 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-606_856-605ins others(24): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885316 | |||||
chr1:56885316
|
A | ATATATAT others(195): Show |
2 | a0001c0001t0001g0061a0001c0001t0001g0065 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.856-606_856-605ins others(202): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885316 | |||||
chr1:56885316
|
ATATATTT others(47): Show |
A | 1 | a0002c0002t0001g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.856-586_856-533del others(54): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885316 | |||||
chr1:56885317
|
T | TATATATT others(23): Show |
1 | a0001c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.856-606_856-605ins others(30): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885317 | |||||
chr1:56885325
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-602T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885325 | ||||||
chr1:56885326
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-601T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885326 | ||||||
chr1:56885326
|
T | G | 6 | a0001c0001t0001g0038a0001c0001t0001g0236a0001c0001t0001g0272others(3): Show | 7 | HG02155.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-601T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885326 | ||||||
chr1:56885341
|
C | T | 5 | a0001c0001t0001g0093a0007c0007t0004g0052a0007c0007t0004g0054others(2): Show | 5 | HG01192.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-586C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885341 | ||||||
chr1:56885342
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(73): Show | 102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.856-585A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885342 | ||||||
chr1:56885342
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-585A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885342 | ||||||
chr1:56885345
|
AAT | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-575_856-574del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885345 | |||||
chr1:56885346
|
ATATATAT others(17): Show |
A | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(64): Show | 93 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.856-575_856-552del others(24): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885346 | |||||
chr1:56885348
|
ATATATTT others(15): Show |
A | 2 | a0001c0001t0001g0131a0007c0007t0004g0055 | 2 | HG00609.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.856-569_856-548del others(22): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885348 | |||||
chr1:56885354
|
TTATGTAA others(59): Show |
T | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.856-569_856-504del others(66): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885354 | |||||
chr1:56885357
|
T | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0093a0007c0007t0004g0052others(3): Show | 7 | HG01192.hp1 HG01891.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-570T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885357 | ||||||
chr1:56885358
|
G | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0086a0001c0010t0001g0231others(2): Show | 6 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.856-569G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885358 | ||||||
chr1:56885358
|
G | T | 193 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(190): Show | 243 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.856-569G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885358 | ||||||
chr1:56885361
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-566A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885361 | ||||||
chr1:56885363
|
T | TTTACATA others(51): Show |
1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-564_856-563ins others(58): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885363 | ||||||
chr1:56885364
|
ATATATT | A | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-553_856-548del others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885364 | |||||
chr1:56885365
|
T | A | 1 | a0002c0002t0001g0157 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.856-562T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885365 | ||||||
chr1:56885366
|
AT | A | 3 | a0001c0001t0003g0207a0001c0001t0003g0208a0003c0003t0002g0081 | 3 | HG01109.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.856-560delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885366 | ||||||
chr1:56885367
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-560T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885367 | ||||||
chr1:56885370
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-557T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885370 | ||||||
chr1:56885370
|
T | TTACATAA others(3): Show |
7 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 8 | HG01891.hp1 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-555_856-554ins others(10): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTACATAA others(57): Show |
1 | a0006c0006t0001g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.856-555_856-554ins others(64): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(9): Show |
1 | a0001c0001t0001g0267 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.856-548_856-533dup others(16): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(25): Show |
3 | a0002c0002t0001g0192a0004c0004t0001g0232a0004c0004t0001g0233 | 3 | HG00280.hp1 HG00558.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.856-528_856-497dup others(32): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(25): Show |
3 | a0001c0001t0001g0080a0001c0001t0001g0084a0018c0017t0002g0079 | 3 | HG02622.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.856-533_856-532ins others(32): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(301): Show |
1 | a0001c0001t0001g0064 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.856-533_856-532ins others(308): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(271): Show |
1 | a0001c0001t0001g0015 | 2 | NA18942.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.856-533_856-532ins others(278): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(207): Show |
1 | a0001c0001t0001g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.856-533_856-532ins others(214): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(239): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0067a0001c0001t0001g0227others(1): Show | 10 | HG00408.hp2 NA18944.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.856-533_856-532ins others(246): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(271): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0114 | 4 | HG02015.hp1 NA18992.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-533_856-532ins others(278): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(271): Show |
1 | a0001c0001t0001g0063 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.856-533_856-532ins others(278): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(271): Show |
1 | a0001c0001t0001g0062 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.856-533_856-532ins others(278): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885370
|
T | TTATATTT others(143): Show |
1 | a0001c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.856-533_856-532ins others(150): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | |||||
chr1:56885373
|
T | C | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0120others(4): Show | 7 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.856-554T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885373 | ||||||
chr1:56885374
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.856-553A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885374 | ||||||
chr1:56885374
|
ATTTATT | A | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0120others(4): Show | 7 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.856-551_856-546del others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885374 | |||||
chr1:56885380
|
T | A | 5 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264others(2): Show | 6 | HG02559.hp1 HG02615.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.856-547T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885380 | ||||||
chr1:56885387
|
T | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-540T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885387 | ||||||
chr1:56885392
|
TTAAATAA others(21): Show |
T | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0003c0003t0002g0219others(1): Show | 4 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-532_856-505del others(28): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885392 | |||||
chr1:56885395
|
A | AATAAATA others(57): Show |
3 | a0001c0001t0001g0268a0003c0003t0002g0228a0006c0006t0001g0266 | 3 | HG02976.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.856-501_856-500ins others(64): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885395 | |||||
chr1:56885395
|
A | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 166 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.856-532A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885395 | ||||||
chr1:56885395
|
A | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG02559.hp1 NA18940.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-532A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885395 | ||||||
chr1:56885396
|
A | G | 9 | a0001c0001t0001g0106a0001c0001t0001g0120a0001c0001t0001g0121others(6): Show | 9 | HG00621.hp1 HG02735.hp2 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.856-531A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885396 | ||||||
chr1:56885396
|
ATAAATAT others(21): Show |
A | 2 | a0001c0001t0001g0254a0002c0002t0001g0028 | 3 | HG00423.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.856-516_856-489del others(28): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885396 | |||||
chr1:56885399
|
AATATATA others(25): Show |
A | 1 | a0010c0012t0001g0204 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.856-523_856-492del others(32): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885399 | |||||
chr1:56885403
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(66): Show | 95 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.856-524T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885403 | ||||||
chr1:56885408
|
TTATTTAA others(5): Show |
T | 29 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(26): Show | 32 | HG00642.hp2 HG00673.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.856-499_856-488del others(12): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885408 | |||||
chr1:56885411
|
T | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-516T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885411 | ||||||
chr1:56885412
|
T | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-515T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885412 | ||||||
chr1:56885417
|
TATATATT others(55): Show |
T | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-503_856-442del others(62): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885417 | |||||
chr1:56885424
|
T | TTACGTAA others(15): Show |
1 | a0007c0007t0004g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.856-501_856-500ins others(22): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885424 | |||||
chr1:56885427
|
A | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 94 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.856-500A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885427 | ||||||
chr1:56885427
|
AAT | A | 9 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0084others(6): Show | 10 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.856-493_856-492del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885427 | |||||
chr1:56885428
|
A | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(45): Show | 67 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.856-499A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885428 | ||||||
chr1:56885429
|
T | TAAATATA others(23): Show |
1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.856-497_856-496ins others(30): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885429 | |||||
chr1:56885429
|
T | TAAATATA others(23): Show |
9 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0003g0077others(6): Show | 9 | HG01109.hp2 HG02109.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-497_856-496ins others(30): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885429 | |||||
chr1:56885429
|
T | TAAATATA others(55): Show |
5 | a0001c0001t0001g0073a0001c0001t0001g0074a0003c0003t0002g0016others(2): Show | 6 | HG01243.hp2 HG02280.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.856-497_856-496ins others(62): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885429 | |||||
chr1:56885429
|
T | TAAATATA others(55): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(2): Show | 10 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.856-497_856-496ins others(62): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885429 | |||||
chr1:56885431
|
T | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(45): Show | 67 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.856-496T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885431 | ||||||
chr1:56885433
|
TATTTAAG others(39): Show |
T | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(45): Show | 67 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.856-491_856-446del others(46): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885433 | |||||
chr1:56885439
|
A | C | 210 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(207): Show | 261 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.856-488A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885439 | ||||||
chr1:56885440
|
G | GTAAATAT others(29): Show |
1 | a0004c0004t0001g0043 | 2 | HG00408.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.856-475_856-440dup others(36): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885440 | |||||
chr1:56885441
|
T | G | 2 | a0002c0002t0001g0190a0007c0007t0004g0055 | 2 | HG03831.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.856-486T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885441 | ||||||
chr1:56885443
|
AAT | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 38 | HG00642.hp2 HG00673.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.856-473_856-472del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885443 | |||||
chr1:56885458
|
C | A | 1 | a0007c0007t0004g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.856-469C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885458 | ||||||
chr1:56885460
|
GTAAA | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.856-464_856-461del others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885460 | |||||
chr1:56885467
|
TATATTTA others(25): Show |
T | 25 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 28 | HG00642.hp2 HG00673.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.856-455_856-424del others(32): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885467 | |||||
chr1:56885475
|
T | A | 1 | a0007c0007t0004g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.856-452T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885475 | ||||||
chr1:56885476
|
T | A | 1 | a0007c0007t0004g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.856-451T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885476 | ||||||
chr1:56885490
|
A | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(48): Show | 70 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.856-437A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885490 | ||||||
chr1:56885492
|
G | A | 1 | a0003c0003t0002g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.856-435G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885492 | ||||||
chr1:56885499
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(58): Show | 80 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.856-428C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885499 | ||||||
chr1:56885555
|
G | GT | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(77): Show | 107 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.856-363dupT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885555 | |||||
chr1:56885565
|
G | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG01168.hp2 HG01433.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-362G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885565 | ||||||
chr1:56885629
|
G | A | 14 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0083others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.856-298G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885629 | ||||||
chr1:56885665
|
C | T | 1 | a0002c0002t0001g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856-262C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885665 | ||||||
chr1:56885772
|
G | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0058others(8): Show | 13 | HG00423.hp1 HG00735.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.856-155G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885772 | ||||||
chr1:56885815
|
G | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(50): Show | 70 | HG00408.hp2 HG01109.hp2 HG01243.hp2 others(67): Show |
intron_variant | MODIFIER | c.856-112G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885815 | ||||||
chr1:56885908
|
C | T | 2 | a0003c0003t0002g0219a0016c0019t0001g0209 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.856-19C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885908 | ||||||
chr1:56885915
|
G | A | 1 | a0015c0021t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.856-12G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885915 | ||||||
chr1:56886270
|
T | C | 4 | a0002c0002t0001g0009a0002c0002t0001g0029a0002c0002t0001g0057others(1): Show | 7 | HG00280.hp2 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096+103T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886270 | ||||||
chr1:56886286
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1096+119T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886286 | ||||||
chr1:56886313
|
T | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0157 | 3 | NA18943.hp1 NA18960.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1096+146T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886313 | ||||||
chr1:56886415
|
T | A | 3 | a0001c0001t0001g0005a0001c0001t0003g0017a0001c0001t0003g0076 | 7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096+248T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886415 | ||||||
chr1:56886520
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(69): Show | 98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1096+353C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886520 | ||||||
chr1:56886600
|
A | T | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+433A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886600 | ||||||
chr1:56886625
|
C | T | 1 | a0002c0002t0001g0186 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1096+458C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886625 | ||||||
chr1:56886681
|
A | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(79): Show | 108 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1096+514A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886681 | ||||||
chr1:56886876
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1096+709G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886876 | ||||||
chr1:56886998
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1096+831A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886998 | ||||||
chr1:56887084
|
T | A | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1096+917T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887084 | ||||||
chr1:56887183
|
A | G | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+1016A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887183 | ||||||
chr1:56887321
|
C | A | 2 | a0002c0002t0001g0138a0002c0002t0001g0191 | 2 | HG02165.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1096+1154C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887321 | ||||||
chr1:56887321
|
C | T | 4 | a0001c0001t0001g0093a0002c0002t0001g0148a0002c0002t0001g0149others(1): Show | 5 | HG01192.hp1 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+1154C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887321 | ||||||
chr1:56887469
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1096+1302T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887469 | ||||||
chr1:56887664
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1096+1497C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887664 | ||||||
chr1:56887738
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1096+1571G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887738 | ||||||
chr1:56887829
|
T | C | 2 | a0001c0001t0001g0093a0004c0004t0001g0039 | 3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1096+1662T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887829 | ||||||
chr1:56887848
|
C | T | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1096+1681C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887848 | ||||||
chr1:56887922
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1096+1755G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887922 | ||||||
chr1:56887982
|
G | A | 1 | a0007c0007t0004g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1096+1815G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887982 | ||||||
chr1:56888049
|
T | A | 1 | a0001c0001t0001g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1096+1882T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888049 | ||||||
chr1:56888121
|
T | A | 1 | a0003c0003t0002g0041 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1096+1954T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888121 | ||||||
chr1:56888162
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(79): Show | 108 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1096+1995C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888162 | ||||||
chr1:56888175
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1096+2008G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888175 | ||||||
chr1:56888175
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1096+2008G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888175 | ||||||
chr1:56888199
|
T | A | 1 | a0001c0001t0001g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2032T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888199 | ||||||
chr1:56888325
|
G | A | 2 | a0002c0002t0001g0173a0014c0022t0002g0220 | 2 | HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1096+2158G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888325 | ||||||
chr1:56888339
|
T | G | 2 | a0009c0013t0002g0174a0009c0013t0002g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1096+2172T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888339 | ||||||
chr1:56888400
|
G | T | 2 | a0003c0003t0002g0219a0016c0019t0001g0209 | 2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1096+2233G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888400 | ||||||
chr1:56888417
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2250T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888417 | ||||||
chr1:56888419
|
G | T | 1 | a0001c0001t0001g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2252G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888419 | ||||||
chr1:56888421
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2254T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888421 | ||||||
chr1:56888543
|
A | G | 84 | a0001c0001t0001g0195a0002c0002t0001g0001a0002c0002t0001g0009others(81): Show | 106 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1096+2376A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888543 | ||||||
chr1:56888612
|
A | C | 1 | a0001c0001t0001g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2445A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888612 | ||||||
chr1:56888613
|
C | A | 1 | a0001c0001t0001g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2446C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888613 | ||||||
chr1:56888614
|
A | C | 1 | a0001c0001t0001g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2447A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888614 | ||||||
chr1:56888629
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1096+2462G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888629 | ||||||
chr1:56888634
|
A | T | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1096+2467A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888634 | ||||||
chr1:56888782
|
A | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 294 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.1096+2615A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888782 | ||||||
chr1:56889080
|
G | T | 1 | a0001c0001t0001g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2913G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889080 | ||||||
chr1:56889082
|
T | A | 1 | a0001c0001t0001g0227 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2915T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889082 | ||||||
chr1:56889128
|
C | T | 6 | a0001c0001t0001g0234a0004c0004t0001g0043a0004c0004t0001g0045others(3): Show | 8 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096+2961C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889128 | ||||||
chr1:56889174
|
T | C | 1 | a0002c0002t0001g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1096+3007T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889174 | ||||||
chr1:56889325
|
A | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(50): Show | 70 | HG00408.hp2 HG01109.hp2 HG01243.hp2 others(67): Show |
intron_variant | MODIFIER | c.1096+3158A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889325 | ||||||
chr1:56889396
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1096+3229G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889396 | ||||||
chr1:56889484
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0254 | 3 | HG00423.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1096+3317C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889484 | ||||||
chr1:56889489
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1096+3322G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889489 | ||||||
chr1:56889509
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1096+3342T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889509 | ||||||
chr1:56889762
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(8): Show | 20 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1096+3595C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889762 | ||||||
chr1:56889797
|
T | G | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+3630T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889797 | ||||||
chr1:56890175
|
C | T | 7 | a0001c0001t0001g0073a0001c0001t0001g0074a0003c0003t0002g0016others(4): Show | 9 | HG01891.hp1 HG02280.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1096+4008C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890175 | ||||||
chr1:56890259
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1096+4092C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890259 | ||||||
chr1:56890290
|
C | T | 7 | a0002c0002t0001g0028a0002c0002t0001g0035a0002c0002t0001g0036others(4): Show | 10 | HG00438.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096+4123C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890290 | ||||||
chr1:56890551
|
C | G | 1 | a0004c0004t0001g0233 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1096+4384C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890551 | ||||||
chr1:56890605
|
G | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(2): Show | 10 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096+4438G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890605 | ||||||
chr1:56890707
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1096+4540G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890707 | ||||||
chr1:56890731
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1096+4564C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890731 | ||||||
chr1:56890761
|
T | C | 2 | a0001c0010t0001g0231a0001c0010t0001g0263 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1096+4594T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890761 | ||||||
chr1:56890796
|
C | A | 1 | a0001c0018t0001g0123 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1096+4629C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890796 | ||||||
chr1:56890802
|
C | A | 1 | a0001c0001t0003g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1096+4635C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890802 | ||||||
chr1:56890803
|
A | G | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 174 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.1096+4636A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890803 | ||||||
chr1:56890822
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1096+4655C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890822 | ||||||
chr1:56890907
|
T | C | 35 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0080others(32): Show | 37 | HG01109.hp2 HG01192.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.1096+4740T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890907 | ||||||
chr1:56891169
|
A | G | 2 | a0001c0001t0001g0088a0002c0002t0001g0203 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1096+5002A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891169 | ||||||
chr1:56891220
|
T | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0051others(15): Show | 24 | HG01123.hp2 HG01943.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1096+5053T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891220 | ||||||
chr1:56891362
|
A | C | 1 | a0017c0020t0005g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1096+5195A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891362 | ||||||
chr1:56891383
|
G | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0137a0004c0004t0001g0039 | 4 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+5216G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891383 | ||||||
chr1:56891423
|
A | G | 1 | a0002c0002t0001g0164 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1096+5256A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891423 | ||||||
chr1:56891472
|
T | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0134 | 2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1096+5305T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891472 | ||||||
chr1:56891763
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1096+5596T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891763 | ||||||
chr1:56891844
|
G | C | 1 | a0004c0004t0001g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1096+5677G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891844 | ||||||
chr1:56891848
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1096+5681G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891848 | ||||||
chr1:56891849
|
G | C | 2 | a0003c0003t0002g0213a0003c0003t0002g0219 | 2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1096+5682G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891849 | ||||||
chr1:56891976
|
T | C | 1 | a0001c0001t0001g0013 | 2 | HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1096+5809T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891976 | ||||||
chr1:56891986
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1096+5819G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891986 | ||||||
chr1:56892104
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1096+5937C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892104 | ||||||
chr1:56892165
|
C | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0224a0001c0001t0003g0235 | 4 | HG01255.hp2 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+5998C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892165 | ||||||
chr1:56892405
|
G | C | 1 | a0012c0011t0001g0243 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1096+6238G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892405 | ||||||
chr1:56892485
|
G | A | 2 | a0001c0001t0001g0093a0004c0004t0001g0039 | 3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1096+6318G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892485 | ||||||
chr1:56892496
|
G | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0137a0004c0004t0001g0039 | 4 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+6329G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892496 | ||||||
chr1:56893120
|
G | A | 8 | a0001c0001t0001g0093a0001c0001t0001g0137a0004c0004t0001g0039others(5): Show | 9 | HG01192.hp1 HG02451.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+6953G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893120 | ||||||
chr1:56893212
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1096+7045T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893212 | ||||||
chr1:56893488
|
T | G | 32 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(29): Show | 40 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1096+7321T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893488 | ||||||
chr1:56893554
|
G | A | 1 | a0010c0012t0001g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1096+7387G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893554 | ||||||
chr1:56893628
|
A | G | 24 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(21): Show | 32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1096+7461A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893628 | ||||||
chr1:56893642
|
T | A | 1 | a0001c0001t0001g0101 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1096+7475T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893642 | ||||||
chr1:56893645
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0137a0004c0004t0001g0039 | 4 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+7478C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893645 | ||||||
chr1:56894056
|
A | T | 8 | a0001c0001t0001g0093a0001c0001t0001g0137a0004c0004t0001g0039others(5): Show | 9 | HG01192.hp1 HG02451.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+7889A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894056 | ||||||
chr1:56894120
|
T | C | 1 | a0002c0002t0001g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1096+7953T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894120 | ||||||
chr1:56894144
|
A | G | 1 | a0002c0002t0001g0171 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1096+7977A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894144 | ||||||
chr1:56894182
|
C | T | 8 | a0001c0001t0001g0093a0001c0001t0001g0137a0004c0004t0001g0039others(5): Show | 9 | HG01192.hp1 HG02451.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+8015C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894182 | ||||||
chr1:56894255
|
T | G | 90 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0195others(87): Show | 113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1096+8088T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894255 | ||||||
chr1:56894259
|
G | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0137a0004c0004t0001g0039 | 4 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+8092G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894259 | ||||||
chr1:56894391
|
T | C | 1 | a0007c0007t0004g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1096+8224T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894391 | ||||||
chr1:56894413
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1096+8246A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894413 | ||||||
chr1:56894635
|
C | A | 1 | a0002c0002t0001g0188 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1096+8468C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894635 | ||||||
chr1:56894660
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1096+8493A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894660 | ||||||
chr1:56894772
|
C | T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1096+8605C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894772 | ||||||
chr1:56894777
|
T | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 326 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.1096+8610T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894777 | ||||||
chr1:56894875
|
G | C | 1 | a0016c0019t0001g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1096+8708G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894875 | ||||||
chr1:56894966
|
TAAC | T | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+8801_1096+880 others(7): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 56894966 | |||||
chr1:56894969
|
C | A | 1 | a0003c0003t0002g0238 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1096+8802C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894969 | ||||||
chr1:56895170
|
C | T | 2 | a0003c0003t0002g0198a0003c0003t0002g0223 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1096+9003C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895170 | ||||||
chr1:56895351
|
T | C | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+9184T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895351 | ||||||
chr1:56895546
|
A | T | 1 | a0002c0002t0001g0162 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1096+9379A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895546 | ||||||
chr1:56895820
|
G | A | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1096+9653G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895820 | ||||||
chr1:56895940
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(4): Show | 12 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096+9773C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895940 | ||||||
chr1:56896004
|
A | G | 1 | a0002c0002t0001g0161 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1096+9837A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896004 | ||||||
chr1:56896229
|
A | G | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+10062A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896229 | ||||||
chr1:56896315
|
A | T | 30 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(27): Show | 38 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1096+10148A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896315 | ||||||
chr1:56896334
|
T | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(63): Show | 92 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1096+10167T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896334 | ||||||
chr1:56896361
|
G | A | 1 | a0007c0007t0004g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1096+10194G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896361 | ||||||
chr1:56896453
|
T | C | 1 | a0003c0003t0002g0041 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1097-10214T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896453 | ||||||
chr1:56896773
|
G | A | 3 | a0001c0018t0001g0123a0002c0002t0001g0150a0002c0002t0001g0151 | 3 | NA18969.hp2 NA18973.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1097-9894G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896773 | ||||||
chr1:56896948
|
T | C | 1 | a0016c0019t0001g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1097-9719T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896948 | ||||||
chr1:56897025
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0046a0004c0004t0001g0245 | 6 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1097-9642G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897025 | ||||||
chr1:56897114
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(63): Show | 92 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1097-9553C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897114 | ||||||
chr1:56897174
|
A | G | 26 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(23): Show | 28 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1097-9493A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897174 | ||||||
chr1:56897245
|
G | A | 21 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(18): Show | 23 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1097-9422G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897245 | ||||||
chr1:56897247
|
G | A | 1 | a0015c0021t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1097-9420G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897247 | ||||||
chr1:56897287
|
C | T | 2 | a0009c0013t0002g0174a0009c0013t0002g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1097-9380C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897287 | ||||||
chr1:56897364
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(1): Show | 9 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1097-9303G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897364 | ||||||
chr1:56897468
|
G | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 200 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1097-9199G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897468 | ||||||
chr1:56897491
|
C | T | 1 | a0001c0001t0001g0024 | 2 | NA18969.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1097-9176C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897491 | ||||||
chr1:56897536
|
C | T | 14 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0083others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1097-9131C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897536 | ||||||
chr1:56897572
|
T | C | 1 | a0016c0019t0001g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1097-9095T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897572 | ||||||
chr1:56897663
|
C | T | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-9004C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897663 | ||||||
chr1:56897708
|
G | A | 1 | a0004c0004t0001g0039 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1097-8959G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897708 | ||||||
chr1:56897786
|
G | A | 26 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(23): Show | 28 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1097-8881G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897786 | ||||||
chr1:56897821
|
T | C | 25 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(22): Show | 27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-8846T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897821 | ||||||
chr1:56897867
|
G | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 90 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1097-8800G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897867 | ||||||
chr1:56898115
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1097-8552G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898115 | ||||||
chr1:56898161
|
T | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(1): Show | 9 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1097-8506T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898161 | ||||||
chr1:56898255
|
G | T | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-8412G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898255 | ||||||
chr1:56898347
|
G | C | 20 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(17): Show | 22 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1097-8320G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898347 | ||||||
chr1:56898368
|
C | T | 26 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(23): Show | 34 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1097-8299C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898368 | ||||||
chr1:56898377
|
G | A | 1 | a0002c0002t0001g0177 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1097-8290G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898377 | ||||||
chr1:56898382
|
T | C | 1 | a0003c0003t0002g0281 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1097-8285T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898382 | ||||||
chr1:56898455
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1097-8212C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898455 | ||||||
chr1:56898635
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1097-8032T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898635 | ||||||
chr1:56898717
|
T | C | 1 | a0002c0002t0001g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1097-7950T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898717 | ||||||
chr1:56898764
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(4): Show | 12 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1097-7903G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898764 | ||||||
chr1:56898766
|
C | G | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-7901C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898766 | ||||||
chr1:56898767
|
T | A | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-7900T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898767 | ||||||
chr1:56898772
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1097-7895G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898772 | ||||||
chr1:56898805
|
C | T | 1 | a0002c0002t0001g0036 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1097-7862C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898805 | ||||||
chr1:56898808
|
T | A | 3 | a0001c0001t0001g0084a0001c0001t0003g0207a0001c0001t0003g0208 | 3 | HG02717.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1097-7859T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898808 | ||||||
chr1:56898893
|
G | A | 2 | a0003c0003t0002g0213a0003c0003t0002g0219 | 2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1097-7774G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898893 | ||||||
chr1:56898934
|
T | C | 1 | a0002c0002t0001g0150 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1097-7733T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898934 | ||||||
chr1:56898942
|
G | A | 20 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(17): Show | 22 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1097-7725G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898942 | ||||||
chr1:56899089
|
C | T | 1 | a0002c0002t0001g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1097-7578C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899089 | ||||||
chr1:56899139
|
G | A | 71 | a0001c0001t0001g0195a0002c0002t0001g0001a0002c0002t0001g0025others(68): Show | 88 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1097-7528G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899139 | ||||||
chr1:56899145
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1097-7522A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899145 | ||||||
chr1:56899165
|
A | G | 1 | a0002c0002t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1097-7502A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899165 | ||||||
chr1:56899363
|
A | G | 1 | a0004c0004t0001g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1097-7304A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899363 | ||||||
chr1:56899447
|
T | G | 1 | a0005c0005t0002g0182 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1097-7220T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899447 | ||||||
chr1:56899572
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(5): Show | 13 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1097-7095G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899572 | ||||||
chr1:56899592
|
C | T | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-7075C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899592 | ||||||
chr1:56899603
|
G | C | 25 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(22): Show | 27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-7064G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899603 | ||||||
chr1:56899619
|
G | A | 2 | a0001c0001t0001g0088a0002c0002t0001g0203 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1097-7048G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899619 | ||||||
chr1:56899642
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1097-7025C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899642 | ||||||
chr1:56899808
|
T | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(24): Show | 41 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1097-6859T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899808 | ||||||
chr1:56900044
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1097-6623C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900044 | ||||||
chr1:56900056
|
G | A | 25 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(22): Show | 27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-6611G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900056 | ||||||
chr1:56900346
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0278 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1097-6321G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900346 | ||||||
chr1:56900377
|
C | T | 1 | a0015c0021t0001g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1097-6290C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900377 | ||||||
chr1:56900416
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(5): Show | 13 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1097-6251G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900416 | ||||||
chr1:56900450
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1097-6217T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900450 | ||||||
chr1:56900581
|
C | T | 2 | a0002c0002t0001g0033a0002c0002t0001g0172 | 3 | NA18951.hp1 NA18971.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1097-6086C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900581 | ||||||
chr1:56900639
|
T | C | 3 | a0003c0003t0002g0041a0003c0003t0002g0228a0006c0006t0001g0075 | 4 | HG01891.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-6028T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900639 | ||||||
chr1:56900644
|
C | CATGAG | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 324 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.1097-6021_1097-602 others(9): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 56900644 | |||||
chr1:56900764
|
C | T | 1 | a0018c0017t0002g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1097-5903C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900764 | ||||||
chr1:56900770
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1097-5897C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900770 | ||||||
chr1:56900818
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0224a0001c0001t0003g0235 | 4 | HG01255.hp2 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-5849C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900818 | ||||||
chr1:56901195
|
A | G | 20 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(17): Show | 22 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1097-5472A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901195 | ||||||
chr1:56901276
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(5): Show | 13 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1097-5391G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901276 | ||||||
chr1:56901288
|
T | A | 2 | a0001c0001t0001g0088a0002c0002t0001g0203 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1097-5379T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901288 | ||||||
chr1:56901288
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1097-5379T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901288 | ||||||
chr1:56901299
|
G | A | 1 | a0002c0002t0001g0183 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1097-5368G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901299 | ||||||
chr1:56901318
|
G | A | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-5349G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901318 | ||||||
chr1:56901357
|
G | T | 2 | a0014c0022t0002g0220a0015c0021t0001g0072 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1097-5310G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901357 | ||||||
chr1:56901368
|
T | A | 25 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(22): Show | 27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-5299T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901368 | ||||||
chr1:56901944
|
A | G | 25 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0093others(22): Show | 27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-4723A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901944 | ||||||
chr1:56902027
|
T | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 326 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.1097-4640T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56902027 | ||||||
chr1:56902134
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0062a0001c0001t0001g0063 | 4 | HG02071.hp2 HG02135.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097-4533G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56902134 | ||||||
chr1:56902378
|
C | CT | 78 | a0001c0001t0001g0195a0002c0002t0001g0001a0002c0002t0001g0025others(75): Show | 96 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1097-4283dupT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 56902378 | |||||
chr1:56902549
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 150 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1097-4118A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56902549 | ||||||
chr1:56902584
|
G | C | 1 | a0014c0022t0002g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1097-4083G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56902584 | ||||||
chr1:56903121
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.1097-3546G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903121 | ||||||
chr1:56903130
|
C | T | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-3537C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903130 | ||||||
chr1:56903213
|
C | G | 8 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1097-3454C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903213 | ||||||
chr1:56903236
|
GGTAATTT others(2): Show |
G | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-3430_1097-342 others(13): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903236 | ||||||
chr1:56903383
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1097-3284C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903383 | ||||||
chr1:56903442
|
A | G | 1 | a0002c0002t0001g0171 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1097-3225A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903442 | ||||||
chr1:56903500
|
A | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.1097-3167A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903500 | ||||||
chr1:56903517
|
C | T | 1 | a0001c0001t0005g0250 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1097-3150C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903517 | ||||||
chr1:56903541
|
C | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 201 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1097-3126C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903541 | ||||||
chr1:56903773
|
G | C | 1 | a0008c0008t0001g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1097-2894G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903773 | ||||||
chr1:56903865
|
T | C | 8 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1097-2802T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903865 | ||||||
chr1:56903982
|
G | A | 1 | a0003c0003t0002g0094 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1097-2685G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903982 | ||||||
chr1:56903984
|
G | A | 1 | a0001c0001t0005g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1097-2683G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903984 | ||||||
chr1:56904026
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1097-2641T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904026 | ||||||
chr1:56904049
|
T | C | 1 | a0007c0007t0004g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1097-2618T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904049 | ||||||
chr1:56904158
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1097-2509G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904158 | ||||||
chr1:56904165
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1097-2502G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904165 | ||||||
chr1:56904202
|
G | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 228 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.1097-2465G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904202 | ||||||
chr1:56904304
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1097-2363C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904304 | ||||||
chr1:56904351
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1097-2316C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904351 | ||||||
chr1:56904398
|
T | C | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-2269T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904398 | ||||||
chr1:56904479
|
C | T | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-2188C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904479 | ||||||
chr1:56904487
|
C | T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1097-2180C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904487 | ||||||
chr1:56904607
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0237 | 4 | NA18950.hp2 NA18966.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097-2060G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904607 | ||||||
chr1:56904616
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0282 | 2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1097-2051G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904616 | ||||||
chr1:56904644
|
T | A | 30 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(27): Show | 38 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1097-2023T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904644 | ||||||
chr1:56904726
|
A | C | 1 | a0008c0008t0001g0248 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1097-1941A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904726 | ||||||
chr1:56904762
|
A | G | 80 | a0001c0001t0001g0195a0002c0002t0001g0001a0002c0002t0001g0025others(77): Show | 99 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1097-1905A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904762 | ||||||
chr1:56904917
|
A | C | 42 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0080others(39): Show | 43 | HG01109.hp2 HG01192.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.1097-1750A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904917 | ||||||
chr1:56904969
|
G | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0282 | 2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1097-1698G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904969 | ||||||
chr1:56905055
|
AT | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0254a0001c0001t0001g0275others(1): Show | 5 | HG00423.hp1 HG01346.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-1606delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 56905055 | |||||
chr1:56905171
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0225 | 3 | NA18943.hp2 NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1097-1496C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905171 | ||||||
chr1:56905391
|
T | C | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-1276T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905391 | ||||||
chr1:56905460
|
T | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(24): Show | 41 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1097-1207T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905460 | ||||||
chr1:56905638
|
C | T | 2 | a0002c0002t0001g0138a0002c0002t0001g0191 | 2 | HG02165.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1097-1029C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905638 | ||||||
chr1:56905822
|
T | C | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-845T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905822 | ||||||
chr1:56905858
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1097-809T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905858 | ||||||
chr1:56905891
|
C | G | 4 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056others(1): Show | 4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-776C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905891 | ||||||
chr1:56906062
|
C | T | 14 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0083others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1097-605C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906062 | ||||||
chr1:56906074
|
T | C | 5 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0055others(2): Show | 5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-593T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906074 | ||||||
chr1:56906249
|
G | A | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-418G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906249 | ||||||
chr1:56906327
|
T | C | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-340T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906327 | ||||||
chr1:56906443
|
T | C | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-224T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906443 | ||||||
chr1:56906525
|
T | C | 3 | a0001c0010t0001g0231a0001c0010t0001g0263a0001c0010t0001g0264 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-142T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906525 | ||||||
chr1:56906820
|
A | G | 1 | a0002c0002t0001g0147 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1222+28A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56906820 | ||||||
chr1:56906852
|
C | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0224a0001c0001t0003g0235others(3): Show | 7 | HG01255.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+60C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56906852 | ||||||
chr1:56906868
|
AT | A | 4 | a0003c0003t0002g0016a0003c0003t0002g0041a0003c0003t0002g0228others(1): Show | 6 | HG01891.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+84delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 56906868 | |||||
chr1:56906918
|
C | T | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 330 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.1222+126C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56906918 | ||||||
chr1:56907047
|
A | T | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1222+255A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907047 | ||||||
chr1:56907120
|
G | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(25): Show | 36 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1222+328G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907120 | ||||||
chr1:56907124
|
G | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(25): Show | 36 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1222+332G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907124 | ||||||
chr1:56907132
|
G | A | 1 | a0003c0003t0002g0238 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1222+340G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907132 | ||||||
chr1:56907231
|
G | T | 1 | a0002c0002t0001g0092 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1222+439G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907231 | ||||||
chr1:56907244
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(66): Show | 96 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1222+452T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907244 | ||||||
chr1:56907251
|
A | G | 1 | a0017c0020t0005g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1222+459A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907251 | ||||||
chr1:56907275
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0003g0017others(1): Show | 9 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+483G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907275 | ||||||
chr1:56907316
|
C | T | 146 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(143): Show | 183 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.1222+524C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907316 | ||||||
chr1:56907624
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0107 | 2 | HG02165.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1223-332G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907624 | ||||||
chr1:56907666
|
A | ATGAG | 7 | a0002c0002t0001g0185a0003c0003t0002g0094a0003c0003t0002g0104others(4): Show | 7 | HG01123.hp2 HG01943.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1223-286_1223-283d others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 56907666 | |||||
chr1:56907806
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1223-150G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907806 | ||||||
chr1:56907827
|
GAGA | G | 31 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0042others(28): Show | 40 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1223-121_1223-119d others(5): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 56907827 | |||||
chr1:56907871
|
T | C | 1 | a0002c0002t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1223-85T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907871 | ||||||
chr1:56908145
|
G | A | 3 | a0005c0009t0002g0037a0005c0009t0002g0205a0014c0022t0002g0220 | 4 | HG01243.hp2 HG02486.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380+32G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908145 | ||||||
chr1:56908327
|
A | G | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1380+214A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908327 | ||||||
chr1:56908332
|
G | A | 2 | a0004c0004t0001g0239a0004c0004t0001g0240 | 2 | NA18993.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1380+219G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908332 | ||||||
chr1:56908474
|
C | A | 1 | a0005c0005t0002g0181 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1380+361C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908474 | ||||||
chr1:56908609
|
T | C | 8 | a0003c0003t0002g0255a0005c0009t0002g0037a0005c0009t0002g0205others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1380+496T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908609 | ||||||
chr1:56908611
|
C | T | 28 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(25): Show | 31 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1380+498C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908611 | ||||||
chr1:56908623
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1380+510G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908623 | ||||||
chr1:56908662
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1380+549C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908662 | ||||||
chr1:56908843
|
C | G | 5 | a0003c0003t0002g0255a0007c0007t0004g0052a0007c0007t0004g0054others(2): Show | 5 | HG02145.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+730C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908843 | ||||||
chr1:56908861
|
A | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(200): Show | 260 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.1380+748A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908861 | ||||||
chr1:56908904
|
C | T | 2 | a0003c0003t0002g0255a0007c0007t0004g0055 | 2 | HG02145.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1380+791C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908904 | ||||||
chr1:56908936
|
T | C | 1 | a0001c0001t0005g0216 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1380+823T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908936 | ||||||
chr1:56909066
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1380+953C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909066 | ||||||
chr1:56909080
|
G | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0217a0006c0006t0001g0047others(5): Show | 12 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+967G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909080 | ||||||
chr1:56909137
|
A | G | 3 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056 | 3 | HG02735.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1380+1024A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909137 | ||||||
chr1:56909502
|
T | G | 2 | a0001c0001t0001g0265a0002c0002t0001g0211 | 2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1380+1389T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909502 | ||||||
chr1:56909507
|
A | T | 1 | a0002c0002t0001g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1380+1394A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909507 | ||||||
chr1:56909721
|
TG | T | 3 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056 | 3 | HG02735.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1380+1609delG | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909721 | ||||||
chr1:56909723
|
C | A | 3 | a0007c0007t0004g0052a0007c0007t0004g0054a0007c0007t0004g0056 | 3 | HG02735.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1380+1610C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909723 | ||||||
chr1:56909756
|
C | T | 1 | a0002c0002t0001g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1380+1643C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909756 | ||||||
chr1:56909847
|
GA | G | 5 | a0003c0003t0002g0255a0007c0007t0004g0052a0007c0007t0004g0054others(2): Show | 5 | HG02145.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+1737delA | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56909847 | |||||
chr1:56909864
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1380+1751A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909864 | ||||||
chr1:56909871
|
G | A | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1380+1758G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909871 | ||||||
chr1:56909883
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1380+1770T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909883 | ||||||
chr1:56909937
|
C | T | 1 | a0002c0002t0001g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1380+1824C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909937 | ||||||
chr1:56909959
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0063others(4): Show | 11 | HG02071.hp2 NA18947.hp1 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.1380+1846G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909959 | ||||||
chr1:56910045
|
C | A | 78 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(75): Show | 99 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1380+1932C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910045 | ||||||
chr1:56910163
|
A | C | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1380+2050A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910163 | ||||||
chr1:56910198
|
G | A | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1380+2085G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910198 | ||||||
chr1:56910377
|
C | T | 28 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(25): Show | 31 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1381-2026C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910377 | ||||||
chr1:56910410
|
C | A | 1 | a0004c0004t0001g0239 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1381-1993C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910410 | ||||||
chr1:56910611
|
C | T | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1792C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910611 | ||||||
chr1:56910673
|
G | T | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1730G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910673 | ||||||
chr1:56910674
|
G | T | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1729G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910674 | ||||||
chr1:56910837
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1381-1566T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910837 | ||||||
chr1:56910895
|
G | C | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1508G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910895 | ||||||
chr1:56910995
|
A | AT | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1408_1381-140 others(5): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910995 | ||||||
chr1:56911065
|
G | GT | 151 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(148): Show | 201 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.1381-1322dupT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | |||||
chr1:56911065
|
G | GTT | 19 | a0001c0001t0001g0060a0001c0001t0001g0085a0001c0001t0001g0103others(16): Show | 20 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-1323_1381-132 others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | |||||
chr1:56911065
|
G | GTTTTTT | 13 | a0003c0003t0002g0016a0003c0003t0002g0041a0003c0003t0002g0081others(10): Show | 15 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1381-1327_1381-132 others(10): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | |||||
chr1:56911065
|
G | GTTTTTTT | 16 | a0003c0003t0002g0040a0003c0003t0002g0094a0003c0003t0002g0104others(13): Show | 17 | HG01123.hp2 HG01943.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.1381-1328_1381-132 others(11): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | |||||
chr1:56911065
|
G | T | 1 | a0019c0015t0007g0053 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1381-1338G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911065 | ||||||
chr1:56911065
|
GT | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0217others(5): Show | 12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-1322delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | |||||
chr1:56911067
|
T | G | 1 | a0002c0002t0001g0147 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1381-1336T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911067 | ||||||
chr1:56911232
|
G | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0272 | 2 | HG02155.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1381-1171G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911232 | ||||||
chr1:56911409
|
A | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0222a0001c0001t0001g0278 | 3 | HG01192.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1381-994A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911409 | ||||||
chr1:56911423
|
C | T | 1 | a0016c0019t0001g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1381-980C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911423 | ||||||
chr1:56911424
|
G | A | 2 | a0009c0013t0002g0174a0009c0013t0002g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1381-979G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911424 | ||||||
chr1:56911460
|
C | T | 2 | a0001c0001t0001g0088a0002c0002t0001g0203 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1381-943C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911460 | ||||||
chr1:56911476
|
C | G | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-927C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911476 | ||||||
chr1:56911499
|
T | C | 78 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(75): Show | 99 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1381-904T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911499 | ||||||
chr1:56911573
|
G | A | 1 | a0003c0003t0002g0238 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1381-830G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911573 | ||||||
chr1:56911631
|
A | G | 3 | a0006c0006t0001g0075a0006c0006t0001g0273a0015c0021t0001g0072 | 3 | HG03098.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1381-772A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911631 | ||||||
chr1:56911650
|
C | T | 1 | a0003c0003t0002g0223 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1381-753C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911650 | ||||||
chr1:56911663
|
A | G | 1 | a0017c0020t0005g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1381-740A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911663 | ||||||
chr1:56911687
|
T | G | 7 | a0001c0001t0001g0038a0001c0001t0001g0078a0001c0001t0001g0224others(4): Show | 8 | HG01255.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1381-716T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911687 | ||||||
chr1:56911695
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1381-708T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911695 | ||||||
chr1:56911699
|
A | G | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-704A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911699 | ||||||
chr1:56911721
|
T | C | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-682T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911721 | ||||||
chr1:56911799
|
T | C | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-604T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911799 | ||||||
chr1:56911810
|
GACA | G | 8 | a0003c0003t0002g0255a0005c0009t0002g0037a0005c0009t0002g0205others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1381-586_1381-584d others(5): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911810 | |||||
chr1:56911824
|
C | T | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-579C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911824 | ||||||
chr1:56911853
|
G | T | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-550G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911853 | ||||||
chr1:56911906
|
G | A | 78 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(75): Show | 99 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1381-497G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911906 | ||||||
chr1:56911928
|
A | G | 8 | a0003c0003t0002g0255a0005c0009t0002g0037a0005c0009t0002g0205others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1381-475A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911928 | ||||||
chr1:56911933
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1381-470C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911933 | ||||||
chr1:56911974
|
A | G | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-429A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911974 | ||||||
chr1:56911993
|
G | A | 8 | a0003c0003t0002g0255a0005c0009t0002g0037a0005c0009t0002g0205others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1381-410G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911993 | ||||||
chr1:56911997
|
T | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0278 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1381-406T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911997 | ||||||
chr1:56912019
|
C | T | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-384C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912019 | ||||||
chr1:56912095
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0254 | 3 | HG00423.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1381-308T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912095 | ||||||
chr1:56912106
|
G | C | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-297G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912106 | ||||||
chr1:56912137
|
C | T | 249 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(246): Show | 315 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.1381-266C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912137 | ||||||
chr1:56912213
|
C | T | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-190C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912213 | ||||||
chr1:56912336
|
G | A | 3 | a0005c0009t0002g0037a0005c0009t0002g0205a0014c0022t0002g0220 | 4 | HG01243.hp2 HG02486.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-67G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912336 | ||||||
chr1:56912367
|
C | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0126 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1381-36C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912367 | ||||||
chr1:56912661
|
T | G | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+36T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56912661 | ||||||
chr1:56912740
|
T | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(246): Show | 315 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.1603+115T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56912740 | ||||||
chr1:56912782
|
T | G | 9 | a0001c0001t0003g0017a0001c0001t0003g0076a0001c0001t0003g0077others(6): Show | 10 | HG02615.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603+157T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56912782 | ||||||
chr1:56912842
|
C | T | 1 | a0002c0002t0001g0110 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1603+217C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56912842 | ||||||
chr1:56913005
|
T | A | 8 | a0003c0003t0002g0255a0005c0009t0002g0037a0005c0009t0002g0205others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1603+380T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913005 | ||||||
chr1:56913025
|
G | A | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+400G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913025 | ||||||
chr1:56913064
|
A | G | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+439A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913064 | ||||||
chr1:56913131
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0230 | 2 | HG02280.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1603+506G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913131 | ||||||
chr1:56913153
|
A | T | 1 | a0005c0005t0002g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1603+528A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913153 | ||||||
chr1:56913178
|
C | T | 5 | a0001c0001t0001g0012a0002c0002t0001g0032a0002c0002t0001g0178others(2): Show | 8 | HG00733.hp2 HG00738.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+553C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913178 | ||||||
chr1:56913197
|
G | A | 1 | a0001c0001t0001g0050 | 2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1603+572G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913197 | ||||||
chr1:56913292
|
G | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0217a0006c0006t0001g0047others(5): Show | 12 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+667G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913292 | ||||||
chr1:56913362
|
T | C | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+737T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913362 | ||||||
chr1:56913460
|
C | A | 1 | a0002c0002t0001g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1603+835C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913460 | ||||||
chr1:56913495
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1603+870G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913495 | ||||||
chr1:56913651
|
C | T | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1026C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913651 | ||||||
chr1:56913654
|
A | G | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1029A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913654 | ||||||
chr1:56913658
|
CTGTT | C | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1037_1603+104 others(8): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56913658 | |||||
chr1:56913691
|
G | A | 5 | a0003c0003t0002g0255a0007c0007t0004g0052a0007c0007t0004g0054others(2): Show | 5 | HG02145.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603+1066G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913691 | ||||||
chr1:56913728
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 90 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1603+1103T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913728 | ||||||
chr1:56913756
|
G | T | 28 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(25): Show | 31 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603+1131G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913756 | ||||||
chr1:56913966
|
T | C | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1341T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913966 | ||||||
chr1:56913987
|
G | T | 1 | a0019c0015t0007g0053 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1603+1362G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913987 | ||||||
chr1:56913988
|
C | T | 2 | a0001c0001t0001g0086a0002c0002t0001g0149 | 2 | HG03486.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1603+1363C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913988 | ||||||
chr1:56913992
|
C | T | 1 | a0002c0002t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1603+1367C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913992 | ||||||
chr1:56913999
|
T | C | 116 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(113): Show | 141 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.1603+1374T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913999 | ||||||
chr1:56914019
|
C | T | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1394C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914019 | ||||||
chr1:56914061
|
T | C | 21 | a0001c0001t0001g0018a0001c0001t0001g0095a0001c0001t0001g0098others(18): Show | 25 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.1603+1436T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914061 | ||||||
chr1:56914084
|
TAAG | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0048others(15): Show | 23 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1603+1464_1603+146 others(7): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56914084 | |||||
chr1:56914262
|
G | A | 1 | a0002c0002t0001g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1603+1637G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914262 | ||||||
chr1:56914359
|
C | T | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+1734C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914359 | ||||||
chr1:56914378
|
G | T | 3 | a0003c0003t0002g0279a0003c0003t0002g0280a0003c0003t0002g0281 | 3 | HG02145.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1603+1753G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914378 | ||||||
chr1:56914391
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0048others(15): Show | 23 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1603+1766C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914391 | ||||||
chr1:56914479
|
T | C | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+1854T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914479 | ||||||
chr1:56914620
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1603+1995A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914620 | ||||||
chr1:56914734
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1603+2109A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914734 | ||||||
chr1:56914768
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1603+2143G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914768 | ||||||
chr1:56914786
|
C | T | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+2161C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914786 | ||||||
chr1:56914787
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(77): Show | 110 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1603+2162G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914787 | ||||||
chr1:56914797
|
C | A | 2 | a0001c0001t0001g0088a0002c0002t0001g0203 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1603+2172C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914797 | ||||||
chr1:56914886
|
C | T | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+2261C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914886 | ||||||
chr1:56914953
|
C | T | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+2328C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914953 | ||||||
chr1:56914983
|
CT | C | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+2361delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56914983 | |||||
chr1:56915179
|
C | G | 5 | a0003c0003t0002g0255a0007c0007t0004g0052a0007c0007t0004g0054others(2): Show | 5 | HG02145.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1604-2386C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915179 | ||||||
chr1:56915181
|
A | C | 3 | a0001c0001t0003g0077a0001c0001t0003g0207a0001c0001t0003g0208 | 3 | HG02717.hp1 HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1604-2384A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915181 | ||||||
chr1:56915212
|
A | G | 1 | a0003c0003t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1604-2353A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915212 | ||||||
chr1:56915291
|
T | A | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1604-2274T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915291 | ||||||
chr1:56915312
|
A | G | 36 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1604-2253A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915312 | ||||||
chr1:56915757
|
T | G | 8 | a0003c0003t0002g0255a0005c0009t0002g0037a0005c0009t0002g0205others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1604-1808T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915757 | ||||||
chr1:56915779
|
C | T | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1604-1786C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915779 | ||||||
chr1:56916060
|
G | C | 1 | a0002c0002t0001g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1604-1505G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916060 | ||||||
chr1:56916060
|
G | T | 4 | a0002c0002t0001g0009a0002c0002t0001g0029a0002c0002t0001g0057others(1): Show | 7 | HG00280.hp2 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1604-1505G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916060 | ||||||
chr1:56916231
|
C | T | 2 | a0004c0004t0001g0232a0004c0004t0001g0233 | 2 | HG00280.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1604-1334C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916231 | ||||||
chr1:56916274
|
C | T | 29 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(26): Show | 32 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.1604-1291C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916274 | ||||||
chr1:56916790
|
ACTCAGGC others(4): Show |
A | 8 | a0003c0003t0002g0255a0005c0009t0002g0037a0005c0009t0002g0205others(5): Show | 9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1604-773_1604-763d others(13): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56916790 | |||||
chr1:56916869
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0217a0006c0006t0001g0047others(4): Show | 11 | HG02622.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1604-696C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916869 | ||||||
chr1:56916880
|
C | G | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1604-685C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916880 | ||||||
chr1:56916897
|
C | T | 37 | a0003c0003t0002g0016a0003c0003t0002g0040a0003c0003t0002g0041others(34): Show | 41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1604-668C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916897 | ||||||
chr1:56916959
|
T | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0230others(3): Show | 10 | HG00323.hp2 HG00735.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1604-606T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916959 | ||||||
chr1:56917045
|
CTG | C | 18 | a0001c0001t0001g0218a0004c0004t0001g0039a0004c0004t0001g0043others(15): Show | 21 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1604-516_1604-515d others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56917045 | |||||
chr1:56917059
|
C | A | 1 | a0002c0002t0001g0192 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1604-506C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56917059 | ||||||
chr1:56917072
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(59): Show | 87 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.1604-493C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56917072 |