geneid | 2017 |
---|---|
ensemblid | ENSG00000085733.16 |
hgncid | 3338 |
symbol | CTTN |
name | cortactin |
refseq_nuc | NM_005231.4 |
refseq_prot | NP_005222.2 |
ensembl_nuc | ENST00000301843.13 |
ensembl_prot | ENSP00000301843.8 |
mane_status | MANE Select |
chr | chr11 |
start | 70398529 |
end | 70436575 |
strand | + |
ver | v1.2 |
region | chr11:70398529-70436575 |
region5000 | chr11:70393529-70441575 |
regionname0 | CTTN_chr11_70398529_70436575 |
regionname5000 | CTTN_chr11_70393529_70441575 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 550 | 300 | 77 | 60 | 111 | 16 | 34 | 74 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0002 | 0/0 | 550 | 18 | 18 | 0 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0003 | 0/0 | 550 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0004 | 0/0 | 550 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0005 | 0/0 | 550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1653 | 189 | 43 | 33 | 90 | 6 | 15 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0002 | 0/0 | 1653 | 56 | 24 | 13 | 5 | 3 | 11 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0003 | 0/0 | 1653 | 42 | 3 | 12 | 15 | 6 | 6 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0004 | 0/0 | 1653 | 18 | 18 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0005 | 0/0 | 1653 | 4 | 0 | 2 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0006 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0007 | 0/0 | 1653 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0008 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0009 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0010 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0011 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0012 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0013 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0014 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0015 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
c0016 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1597 | 153 | 19 | 30 | 83 | 6 | 13 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0002 | 0/0 | 1598 | 50 | 16 | 13 | 10 | 1 | 10 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0003 | 0/0 | 1596 | 15 | 15 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0004 | 0/0 | 1597 | 15 | 15 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0005 | 0/0 | 1594 | 12 | 3 | 2 | 1 | 2 | 4 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0006 | 0/0 | 1594 | 12 | 0 | 1 | 9 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0007 | 0/0 | 1596 | 11 | 9 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0008 | 0/0 | 1595 | 9 | 0 | 9 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0009 | 0/0 | 1599 | 7 | 2 | 2 | 1 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0010 | 0/0 | 1598 | 4 | 1 | 0 | 2 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0011 | 0/0 | 1594 | 3 | 0 | 0 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0012 | 0/0 | 1597 | 3 | 3 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0013 | 0/0 | 1595 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0014 | 0/0 | 1596 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0015 | 0/0 | 1595 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0016 | 0/0 | 1597 | 2 | 0 | 1 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0017 | 0/0 | 1595 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0018 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0019 | 0/0 | 1597 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0020 | 0/0 | 1599 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0021 | 0/0 | 1595 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0022 | 0/0 | 1595 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0023 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0024 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0025 | 0/0 | 1597 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0026 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0027 | 0/0 | 1594 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0028 | 0/0 | 1595 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0029 | 0/0 | 1597 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0030 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0031 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0032 | 0/0 | 1599 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0033 | 0/0 | 1597 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0034 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0035 | 0/0 | 1597 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
t0036 | 0/0 | 1594 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 1 | 6 | 2 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0002 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0003 | 0/0 | 7 | 1 | 5 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0005 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0006 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0008 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0037 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1653 | 189 | 43 | 33 | 90 | 6 | 15 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0002 | 0/0 | 1653 | 56 | 24 | 13 | 5 | 3 | 11 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003 | 0/0 | 1653 | 42 | 3 | 12 | 15 | 6 | 6 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0005 | 0/0 | 1653 | 4 | 0 | 2 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0006 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0009 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0010 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0011 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0013 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0014 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0015 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0016 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0002c0004 | 0/0 | 1653 | 18 | 18 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0003c0007 | 0/0 | 1653 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0004c0012 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0005c0008 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3249 | 137 | 9 | 29 | 79 | 5 | 13 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0002 | 0/0 | 3250 | 10 | 1 | 2 | 7 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0003 | 0/0 | 3248 | 14 | 14 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0007 | 0/0 | 3248 | 10 | 8 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0013 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0014 | 0/0 | 3248 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0015 | 0/0 | 3247 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0016 | 0/0 | 3249 | 2 | 0 | 1 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0017 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0021 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0022 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0023 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0024 | 0/0 | 3249 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0025 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0026 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0030 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0031 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0034 | 0/0 | 3248 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0001t0035 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0002t0001 | 0/0 | 3249 | 10 | 8 | 1 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0002t0002 | 0/0 | 3250 | 34 | 14 | 9 | 2 | 1 | 8 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0002t0009 | 0/0 | 3251 | 7 | 2 | 2 | 1 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0002t0010 | 0/0 | 3250 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0002t0020 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0002t0032 | 0/0 | 3251 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0002t0033 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0001 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0005 | 0/0 | 3246 | 12 | 3 | 2 | 1 | 2 | 4 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0006 | 0/0 | 3246 | 12 | 0 | 1 | 9 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0008 | 0/0 | 3247 | 9 | 0 | 9 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0011 | 0/0 | 3246 | 3 | 0 | 0 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0019 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0027 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0028 | 0/0 | 3247 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0029 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0003t0036 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0005t0002 | 0/0 | 3250 | 4 | 0 | 2 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0006t0012 | 0/0 | 3249 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0009t0001 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0010t0002 | 0/0 | 3250 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0011t0012 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0013t0013 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0014t0007 | 0/0 | 3248 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0015t0003 | 0/0 | 3248 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0001c0016t0010 | 0/0 | 3250 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0002c0004t0001 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0002c0004t0002 | 0/0 | 3250 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0002c0004t0004 | 0/0 | 3249 | 14 | 14 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0002c0004t0010 | 0/0 | 3250 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0002c0004t0018 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0003c0007t0001 | 0/0 | 3249 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0004c0012t0001 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
a0005c0008t0004 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | copy fasta | chr11 | 70393529 | 70441575 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 1 | 6 | 2 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0037 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0007g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0014g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0014g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0016g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0016g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0017g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0021g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0022g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0023g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0024g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0025g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0026g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0030g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0031g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0034g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0001t0035g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0003 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0008 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0009g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0009g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0009g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0009g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0010g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0020g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0032g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0002t0033g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0005g0006 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0005g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0008g0005 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0008g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0011g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0019g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0027g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0028g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0029g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0003t0036g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0005t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0005t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0005t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0006t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0006t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0009t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0010t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0011t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0013t0013g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0014t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0015t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0001c0016t0010g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0004g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0002c0004t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0003c0007t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0003c0007t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0004c0012t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
a0005c0008t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0005 | g0014 | EUR | GBR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00099 | hp2 | a0001 | c0016 | t0010 | g0068 | EUR | GBR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00280 | hp1 | a0001 | c0002 | t0009 | g0227 | EUR | FIN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00323 | hp1 | a0001 | c0003 | t0028 | g0144 | EUR | FIN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00558 | hp1 | a0001 | c0002 | t0010 | g0060 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00733 | hp1 | a0001 | c0002 | t0009 | g0225 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00735 | hp1 | a0001 | c0003 | t0008 | g0063 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00735 | hp2 | a0001 | c0001 | t0024 | g0216 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01074 | hp1 | a0001 | c0003 | t0006 | g0131 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01074 | hp2 | a0001 | c0002 | t0032 | g0093 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01106 | hp1 | a0001 | c0003 | t0005 | g0006 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01175 | hp1 | a0001 | c0003 | t0008 | g0067 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01243 | hp2 | a0001 | c0005 | t0002 | g0025 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01256 | hp1 | a0001 | c0003 | t0008 | g0006 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01257 | hp1 | a0001 | c0002 | t0009 | g0003 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01346 | hp2 | a0001 | c0005 | t0002 | g0025 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01496 | hp1 | a0001 | c0001 | t0016 | g0169 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01515 | hp1 | a0001 | c0001 | t0025 | g0166 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0040 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01516 | hp2 | a0001 | c0003 | t0029 | g0141 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01517 | hp1 | a0001 | c0003 | t0027 | g0139 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0040 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01884 | hp2 | a0002 | c0004 | t0004 | g0101 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01891 | hp1 | a0001 | c0003 | t0005 | g0006 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01934 | hp2 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01943 | hp2 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01981 | hp2 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01993 | hp1 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02027 | hp2 | a0001 | c0003 | t0006 | g0024 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02080 | hp1 | a0001 | c0003 | t0006 | g0136 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02083 | hp2 | a0001 | c0003 | t0006 | g0022 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02132 | hp1 | a0001 | c0003 | t0005 | g0069 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0112 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02148 | hp2 | a0001 | c0003 | t0005 | g0006 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02257 | hp2 | a0001 | c0003 | t0005 | g0061 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02258 | hp2 | a0002 | c0004 | t0004 | g0100 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02273 | hp1 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02280 | hp1 | a0001 | c0015 | t0003 | g0050 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02300 | hp2 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0236 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02523 | hp2 | a0001 | c0003 | t0006 | g0138 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02572 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0081 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02630 | hp1 | a0005 | c0008 | t0004 | g0234 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0080 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02647 | hp1 | a0002 | c0004 | t0004 | g0020 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0219 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0127 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02717 | hp2 | a0001 | c0001 | t0026 | g0118 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02735 | hp1 | a0001 | c0003 | t0005 | g0066 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02735 | hp2 | a0001 | c0005 | t0002 | g0071 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0237 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02809 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02895 | hp1 | a0002 | c0004 | t0004 | g0233 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0117 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02896 | hp2 | a0001 | c0014 | t0007 | g0086 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02897 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02922 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02965 | hp1 | a0001 | c0001 | t0015 | g0015 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03041 | hp1 | a0001 | c0009 | t0001 | g0105 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0226 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03098 | hp1 | a0002 | c0004 | t0010 | g0004 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03098 | hp2 | a0001 | c0002 | t0009 | g0017 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03130 | hp1 | a0002 | c0004 | t0004 | g0004 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03130 | hp2 | a0002 | c0004 | t0018 | g0020 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0085 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03209 | hp1 | a0002 | c0004 | t0004 | g0240 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0083 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03225 | hp1 | a0001 | c0001 | t0022 | g0238 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03239 | hp2 | a0001 | c0003 | t0005 | g0064 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03453 | hp2 | a0001 | c0006 | t0012 | g0076 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03486 | hp1 | a0001 | c0001 | t0015 | g0097 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03486 | hp2 | a0002 | c0004 | t0004 | g0235 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0126 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03516 | hp1 | a0001 | c0001 | t0021 | g0232 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0239 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03540 | hp1 | a0002 | c0004 | t0001 | g0078 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03579 | hp2 | a0001 | c0001 | t0013 | g0049 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03654 | hp1 | a0001 | c0002 | t0033 | g0123 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03654 | hp2 | a0001 | c0001 | t0016 | g0029 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03688 | hp1 | a0001 | c0003 | t0005 | g0062 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03710 | hp1 | a0001 | c0005 | t0002 | g0149 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03710 | hp2 | a0001 | c0001 | t0035 | g0148 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0122 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0228 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03927 | hp1 | a0001 | c0002 | t0020 | g0059 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03927 | hp2 | a0001 | c0002 | t0009 | g0121 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0124 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG04115 | hp2 | a0001 | c0003 | t0006 | g0024 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG04184 | hp2 | a0001 | c0003 | t0005 | g0014 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG04228 | hp1 | a0001 | c0003 | t0019 | g0058 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0073 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18612 | hp1 | a0004 | c0012 | t0001 | g0188 | EAS | CHB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18906 | hp2 | a0001 | c0002 | t0009 | g0087 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18942 | hp2 | a0001 | c0001 | t0007 | g0181 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18946 | hp2 | a0001 | c0002 | t0010 | g0070 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18948 | hp1 | a0001 | c0003 | t0006 | g0230 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18953 | hp1 | a0001 | c0003 | t0006 | g0022 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18966 | hp1 | a0003 | c0007 | t0001 | g0113 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18977 | hp1 | a0001 | c0002 | t0009 | g0119 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18979 | hp1 | a0003 | c0007 | t0001 | g0114 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18995 | hp1 | a0001 | c0003 | t0036 | g0130 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18997 | hp2 | a0001 | c0003 | t0011 | g0057 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19001 | hp2 | a0001 | c0001 | t0030 | g0212 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19004 | hp1 | a0001 | c0003 | t0006 | g0137 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19011 | hp1 | a0001 | c0003 | t0006 | g0142 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19043 | hp1 | a0002 | c0004 | t0004 | g0042 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19057 | hp2 | a0001 | c0003 | t0011 | g0072 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19062 | hp1 | a0001 | c0003 | t0006 | g0129 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19066 | hp2 | a0001 | c0003 | t0011 | g0065 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19077 | hp2 | a0001 | c0001 | t0031 | g0021 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19084 | hp2 | a0001 | c0010 | t0002 | g0205 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19089 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA19240 | hp2 | a0001 | c0006 | t0012 | g0075 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ASW | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA20129 | hp2 | a0001 | c0001 | t0034 | g0220 | AFR | ASW | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA20752 | hp2 | a0001 | c0003 | t0006 | g0143 | EUR | TSI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA20805 | hp2 | a0001 | c0003 | t0005 | g0006 | EUR | TSI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02109 | hp1 | a0002 | c0004 | t0004 | g0042 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02486 | hp1 | a0001 | c0001 | t0023 | g0150 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02559 | hp1 | a0001 | c0003 | t0005 | g0056 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03471 | hp1 | a0001 | c0013 | t0013 | g0044 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | USA | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
HG06807 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | USA | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA20300 | hp1 | a0002 | c0004 | t0002 | g0104 | AFR | USA | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA21309 | hp1 | a0001 | c0011 | t0012 | g0074 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0089 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0037 | REF | REF | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0170 | REF | REF | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:70405267
|
G | A | 1 | a0001 | 1 | HG00735.hp2 | splice_region_variant | LOW | c.-95G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/18 | chr11 | 70405267 | ||||||
chr11:70407334
|
G | A | 1 | a0005 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.37G>A | p.Ala13Thr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/18 | 220/3249 | 37/1653 | 13/550 | chr11 | 70407334 | ||
chr11:70431228
|
C | T | 1 | a0003 | 2 | NA18966.hp1 NA18979.hp1 |
missense_variant | MODERATE | c.1214C>T | p.Ser405Leu | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/18 | 1397/3249 | 1214/1653 | 405/550 | chr11 | 70431228 | ||
chr11:70433653
|
G | A | 2 | a0002a0005 | 19 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
missense_variant | MODERATE | c.1451G>A | p.Ser484Asn | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1634/3249 | 1451/1653 | 484/550 | chr11 | 70433653 | ||
chr11:70433661
|
G | A | 1 | a0004 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.1459G>A | p.Asp487Asn | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1642/3249 | 1459/1653 | 487/550 | chr11 | 70433661 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:70407369
|
C | T | 2 | a0001c0003a0001c0016 | 43 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(40): Show |
synonymous_variant | LOW | c.72C>T | p.Thr24Thr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/18 | 255/3249 | 72/1653 | 24/550 | chr11 | 70407369 | ||
chr11:70419774
|
C | T | 1 | a0001c0005 | 4 | HG01243.hp2 HG01346.hp2 HG02735.hp2 others(1): Show |
synonymous_variant | LOW | c.597C>T | p.Tyr199Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/18 | 780/3249 | 597/1653 | 199/550 | chr11 | 70419774 | ||
chr11:70422974
|
G | A | 1 | a0001c0009 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.936G>A | p.Val312Val | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/18 | 1119/3249 | 936/1653 | 312/550 | chr11 | 70422974 | ||
chr11:70425337
|
G | A | 1 | a0001c0010 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.963G>A | p.Ala321Ala | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/18 | 1146/3249 | 963/1653 | 321/550 | chr11 | 70425337 | ||
chr11:70425352
|
T | C | 1 | a0001c0011 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.978T>C | p.Asp326Asp | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/18 | 1161/3249 | 978/1653 | 326/550 | chr11 | 70425352 | ||
chr11:70429172
|
G | A | 1 | a0005c0008 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1149G>A | p.Glu383Glu | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/18 | 1332/3249 | 1149/1653 | 383/550 | chr11 | 70429172 | ||
chr11:70433133
|
C | T | 1 | a0001c0015 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1299C>T | p.Tyr433Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/18 | 1482/3249 | 1299/1653 | 433/550 | chr11 | 70433133 | ||
chr11:70433166
|
C | T | 1 | a0001c0006 | 2 | HG03453.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.1332C>T | p.Pro444Pro | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/18 | 1515/3249 | 1332/1653 | 444/550 | chr11 | 70433166 | ||
chr11:70433660
|
C | T | 4 | a0001c0002a0001c0005a0001c0014others(1): Show | 62 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(59): Show |
synonymous_variant | LOW | c.1458C>T | p.Tyr486Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1641/3249 | 1458/1653 | 486/550 | chr11 | 70433660 | ||
chr11:70433669
|
C | T | 1 | a0001c0014 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.1467C>T | p.Tyr489Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1650/3249 | 1467/1653 | 489/550 | chr11 | 70433669 | ||
chr11:70433705
|
C | T | 1 | a0001c0013 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1503C>T | p.Tyr501Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1686/3249 | 1503/1653 | 501/550 | chr11 | 70433705 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:70398550
|
T | C | 21 | a0001c0001t0003a0001c0001t0013a0001c0001t0014others(18): Show | 71 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(68): Show |
5_prime_UTR_variant | MODIFIER | c.-162T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/18 | 8748 | chr11 | 70398550 | |||||
chr11:70398555
|
G | A | 1 | a0001c0001t0023 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-157G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/18 | 8743 | chr11 | 70398555 | |||||
chr11:70405299
|
T | C | 1 | a0001c0001t0025 | 1 | HG01515.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/18 | chr11 | 70405299 | ||||||
chr11:70405327
|
C | T | 4 | a0001c0001t0021a0001c0001t0022a0001c0006t0012others(1): Show | 5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-35C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/18 | chr11 | 70405327 | ||||||
chr11:70435173
|
C | G | 1 | a0001c0003t0036 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 11 | chr11 | 70435173 | |||||
chr11:70435177
|
C | G | 1 | a0001c0001t0035 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 15 | chr11 | 70435177 | |||||
chr11:70435178
|
C | A | 1 | a0001c0001t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 16 | chr11 | 70435178 | |||||
chr11:70435178
|
C | G | 2 | a0001c0001t0034a0001c0003t0011 | 4 | NA18997.hp2 NA19057.hp2 NA19066.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*16C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 16 | chr11 | 70435178 | |||||
chr11:70435253
|
G | GT | 8 | a0001c0001t0002a0001c0002t0002a0001c0002t0010others(5): Show | 54 | HG00099.hp2 HG00558.hp1 HG01070.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*116dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 117 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | ||||
chr11:70435253
|
G | GTT | 3 | a0001c0002t0009a0001c0002t0020a0001c0002t0032 | 9 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*115_*116dupTT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 117 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | ||||
chr11:70435253
|
G | T | 1 | a0001c0002t0033 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 91 | chr11 | 70435253 | |||||
chr11:70435253
|
GT | G | 6 | a0001c0001t0003a0001c0001t0007a0001c0001t0014others(3): Show | 29 | HG01891.hp2 HG02055.hp2 HG02135.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*116delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 116 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | ||||
chr11:70435253
|
GTT | G | 8 | a0001c0001t0013a0001c0001t0015a0001c0001t0017others(5): Show | 17 | HG00323.hp1 HG00735.hp1 HG01175.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*115_*116delTT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 115 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | ||||
chr11:70435253
|
GTTT | G | 5 | a0001c0003t0005a0001c0003t0006a0001c0003t0011others(2): Show | 29 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*114_*116delTTT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 114 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | ||||
chr11:70435739
|
G | A | 1 | a0001c0001t0016 | 2 | HG01496.hp1 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*577G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 577 | chr11 | 70435739 | |||||
chr11:70435832
|
G | A | 2 | a0001c0003t0027a0001c0003t0029 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*670G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 670 | chr11 | 70435832 | |||||
chr11:70435995
|
T | C | 1 | a0002c0004t0018 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 833 | chr11 | 70435995 | |||||
chr11:70436001
|
C | T | 2 | a0001c0001t0014a0001c0001t0017 | 3 | HG02451.hp2 HG02809.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*839C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 839 | chr11 | 70436001 | |||||
chr11:70436057
|
G | A | 1 | a0001c0001t0030 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*895G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 895 | chr11 | 70436057 | |||||
chr11:70436099
|
C | T | 1 | a0001c0001t0031 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*937C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 937 | chr11 | 70436099 | |||||
chr11:70436119
|
A | G | 1 | a0001c0001t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*957A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 957 | chr11 | 70436119 | |||||
chr11:70436227
|
C | T | 1 | a0001c0001t0022 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1065C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 1065 | chr11 | 70436227 | |||||
chr11:70436288
|
C | T | 1 | a0001c0002t0032 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1126C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 1126 | chr11 | 70436288 | |||||
chr11:70436523
|
A | C | 9 | a0001c0003t0005a0001c0003t0006a0001c0003t0008others(6): Show | 41 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1361A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 1361 | chr11 | 70436523 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:70398808
|
G | A | 1 | a0001c0002t0002g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-98+194G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70398808 | ||||||
chr11:70398875
|
G | A | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-98+261G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70398875 | ||||||
chr11:70398940
|
G | A | 34 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(31): Show | 46 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-98+326G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70398940 | ||||||
chr11:70398955
|
G | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-98+341G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70398955 | ||||||
chr11:70399020
|
G | C | 2 | a0001c0001t0003g0045a0001c0001t0003g0046 | 2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-98+406G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399020 | ||||||
chr11:70399051
|
A | G | 12 | a0001c0001t0014g0237a0001c0001t0014g0239a0001c0001t0017g0236others(9): Show | 18 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.-98+437A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399051 | ||||||
chr11:70399056
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-98+442C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399056 | ||||||
chr11:70399169
|
G | T | 11 | a0001c0001t0014g0237a0001c0001t0014g0239a0001c0001t0017g0236others(8): Show | 16 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-98+555G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399169 | ||||||
chr11:70399361
|
G | A | 3 | a0001c0001t0007g0015a0001c0001t0007g0073a0001c0001t0015g0015 | 3 | HG02055.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-98+747G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399361 | ||||||
chr11:70399590
|
A | G | 1 | a0002c0004t0004g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-98+976A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399590 | ||||||
chr11:70399641
|
A | G | 1 | a0001c0003t0011g0072 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-98+1027A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399641 | ||||||
chr11:70399664
|
G | A | 3 | a0001c0006t0012g0075a0001c0006t0012g0076a0001c0011t0012g0074 | 3 | HG03453.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-98+1050G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399664 | ||||||
chr11:70399718
|
TGGACGTT others(12): Show |
T | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+1107_-98+1125d others(21): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70399718 | |||||
chr11:70399912
|
A | T | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+1298A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399912 | ||||||
chr11:70400095
|
G | A | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0013g0049 | 3 | HG02717.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-98+1481G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400095 | ||||||
chr11:70400134
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-98+1520A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400134 | ||||||
chr11:70400148
|
T | C | 34 | a0001c0001t0001g0099a0001c0001t0003g0047a0001c0001t0003g0048others(31): Show | 37 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.-98+1534T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400148 | ||||||
chr11:70400262
|
A | T | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+1648A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400262 | ||||||
chr11:70400307
|
A | G | 14 | a0001c0001t0014g0237a0001c0001t0014g0239a0001c0001t0017g0236others(11): Show | 20 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.-98+1693A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400307 | ||||||
chr11:70400613
|
G | A | 8 | a0001c0001t0021g0232a0002c0004t0004g0004a0002c0004t0004g0042others(5): Show | 14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-98+1999G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400613 | ||||||
chr11:70400656
|
G | C | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-98+2042G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400656 | ||||||
chr11:70400830
|
A | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0002g0041 | 6 | HG01928.hp2 HG01943.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-98+2216A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400830 | ||||||
chr11:70400850
|
C | A | 37 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(34): Show | 49 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-98+2236C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400850 | ||||||
chr11:70400855
|
T | A | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+2241T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400855 | ||||||
chr11:70400886
|
C | T | 9 | a0001c0002t0001g0003a0001c0002t0001g0040a0001c0002t0002g0003others(6): Show | 13 | HG00280.hp1 HG00733.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-98+2272C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400886 | ||||||
chr11:70400895
|
C | A | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 5 | HG02145.hp1 HG02258.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-98+2281C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400895 | ||||||
chr11:70400967
|
T | A | 1 | a0001c0002t0002g0102 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-98+2353T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400967 | ||||||
chr11:70401171
|
G | A | 15 | a0001c0001t0014g0237a0001c0001t0014g0239a0001c0001t0017g0236others(12): Show | 21 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.-98+2557G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401171 | ||||||
chr11:70401302
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-98+2688C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401302 | ||||||
chr11:70401306
|
T | TA | 66 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(63): Show | 81 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-98+2703dupA | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70401306 | |||||
chr11:70401314
|
A | C | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-98+2700A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401314 | ||||||
chr11:70401317
|
A | T | 1 | a0001c0001t0001g0223 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-98+2703A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401317 | ||||||
chr11:70401332
|
C | T | 13 | a0001c0001t0014g0237a0001c0001t0014g0239a0001c0001t0017g0236others(10): Show | 19 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.-98+2718C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401332 | ||||||
chr11:70401336
|
C | T | 2 | a0001c0001t0001g0222a0001c0011t0012g0074 | 2 | HG00544.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-98+2722C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401336 | ||||||
chr11:70401565
|
T | C | 8 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0051others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-98+2951T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401565 | ||||||
chr11:70401625
|
G | A | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+3011G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401625 | ||||||
chr11:70401660
|
A | C | 1 | a0001c0001t0002g0221 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-98+3046A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401660 | ||||||
chr11:70401660
|
A | T | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+3046A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401660 | ||||||
chr11:70401661
|
C | A | 1 | a0001c0001t0002g0221 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-98+3047C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401661 | ||||||
chr11:70401819
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-98+3205G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401819 | ||||||
chr11:70401864
|
G | A | 39 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(36): Show | 51 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-98+3250G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401864 | ||||||
chr11:70401967
|
C | A | 1 | a0001c0001t0001g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-97-3298C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401967 | ||||||
chr11:70402007
|
G | C | 31 | a0001c0001t0007g0015a0001c0001t0007g0016a0001c0001t0007g0073others(28): Show | 34 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-97-3258G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402007 | ||||||
chr11:70402022
|
G | A | 2 | a0001c0003t0005g0014a0001c0003t0005g0056 | 3 | HG00099.hp1 HG02559.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-97-3243G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402022 | ||||||
chr11:70402050
|
A | T | 1 | a0001c0001t0015g0097 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-97-3215A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402050 | ||||||
chr11:70402080
|
G | T | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-3185G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402080 | ||||||
chr11:70402162
|
A | C | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-3103A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402162 | ||||||
chr11:70402179
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-97-3086G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402179 | ||||||
chr11:70402187
|
T | C | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-3078T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402187 | ||||||
chr11:70402188
|
C | A | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-3077C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402188 | ||||||
chr11:70402274
|
A | T | 15 | a0001c0001t0014g0237a0001c0001t0014g0239a0001c0001t0017g0236others(12): Show | 21 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.-97-2991A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402274 | ||||||
chr11:70402339
|
A | G | 2 | a0001c0006t0012g0075a0001c0006t0012g0076 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-97-2926A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402339 | ||||||
chr11:70402371
|
C | T | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-2894C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402371 | ||||||
chr11:70402377
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-97-2888G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402377 | ||||||
chr11:70402569
|
A | T | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-2696A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402569 | ||||||
chr11:70402794
|
C | T | 84 | a0001c0001t0001g0099a0001c0001t0003g0010a0001c0001t0003g0013others(81): Show | 104 | HG00099.hp2 HG00558.hp1 HG00735.hp1 others(101): Show |
intron_variant | MODIFIER | c.-97-2471C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402794 | ||||||
chr11:70403036
|
T | A | 1 | a0001c0003t0011g0057 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-97-2229T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403036 | ||||||
chr11:70403186
|
C | CT | 34 | a0001c0001t0001g0012a0001c0001t0001g0099a0001c0001t0001g0211others(31): Show | 45 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-97-2058dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70403186 | |||||
chr11:70403186
|
C | CTT | 7 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0053others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-97-2059_-97-2058d others(4): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70403186 | |||||
chr11:70403186
|
CT | C | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0107others(15): Show | 20 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.-97-2058delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70403186 | |||||
chr11:70403228
|
C | T | 1 | a0001c0001t0022g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-97-2037C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403228 | ||||||
chr11:70403249
|
C | T | 1 | a0001c0001t0022g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-97-2016C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403249 | ||||||
chr11:70403257
|
C | T | 4 | a0001c0001t0013g0049a0001c0002t0002g0077a0001c0002t0002g0218others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-97-2008C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403257 | ||||||
chr11:70403293
|
G | A | 38 | a0001c0001t0013g0049a0001c0001t0014g0239a0001c0001t0022g0238others(35): Show | 53 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.-97-1972G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403293 | ||||||
chr11:70403305
|
C | CAGCCTCC others(2): Show |
89 | a0001c0001t0001g0099a0001c0001t0001g0128a0001c0001t0003g0010others(86): Show | 117 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(114): Show |
intron_variant | MODIFIER | c.-97-1957_-97-1949d others(11): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70403305 | |||||
chr11:70403429
|
C | T | 13 | a0001c0001t0013g0049a0002c0004t0001g0078a0002c0004t0004g0004others(10): Show | 19 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-97-1836C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403429 | ||||||
chr11:70403434
|
G | A | 2 | a0001c0001t0021g0232a0001c0011t0012g0074 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-97-1831G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403434 | ||||||
chr11:70403749
|
C | T | 3 | a0001c0001t0022g0238a0001c0006t0012g0075a0001c0006t0012g0076 | 3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-97-1516C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403749 | ||||||
chr11:70403763
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-97-1502A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403763 | ||||||
chr11:70403771
|
C | T | 5 | a0001c0001t0021g0232a0001c0001t0022g0238a0001c0006t0012g0075others(2): Show | 5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-97-1494C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403771 | ||||||
chr11:70404039
|
C | T | 1 | a0001c0001t0021g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-97-1226C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404039 | ||||||
chr11:70404070
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-97-1195A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404070 | ||||||
chr11:70404206
|
T | A | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-1059T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404206 | ||||||
chr11:70404293
|
A | C | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-972A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404293 | ||||||
chr11:70404419
|
C | G | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-846C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404419 | ||||||
chr11:70404651
|
G | A | 5 | a0001c0001t0021g0232a0001c0001t0022g0238a0001c0006t0012g0075others(2): Show | 5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-97-614G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404651 | ||||||
chr11:70404784
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-97-481C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404784 | ||||||
chr11:70404831
|
C | T | 3 | a0001c0001t0001g0206a0001c0001t0001g0224a0001c0001t0007g0117 | 3 | HG02615.hp1 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-97-434C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404831 | ||||||
chr11:70404942
|
C | T | 1 | a0001c0001t0003g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-97-323C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404942 | ||||||
chr11:70404951
|
G | A | 3 | a0001c0003t0006g0022a0001c0003t0006g0129a0001c0003t0036g0130 | 4 | HG02083.hp2 NA18953.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-97-314G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404951 | ||||||
chr11:70404954
|
A | C | 1 | a0001c0005t0002g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-97-311A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404954 | ||||||
chr11:70405071
|
A | C | 1 | a0001c0001t0026g0118 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-97-194A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405071 | ||||||
chr11:70405076
|
C | T | 2 | a0001c0001t0001g0204a0001c0010t0002g0205 | 2 | HG02015.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-97-189C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405076 | ||||||
chr11:70405140
|
C | G | 3 | a0002c0004t0004g0020a0002c0004t0004g0101a0002c0004t0018g0020 | 3 | HG01884.hp2 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-97-125C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405140 | ||||||
chr11:70405154
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-97-111G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405154 | ||||||
chr11:70405231
|
C | G | 3 | a0001c0001t0022g0238a0001c0006t0012g0075a0001c0006t0012g0076 | 3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-97-34C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405231 | ||||||
chr11:70405255
|
C | G | 1 | a0002c0004t0001g0078 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-97-10C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405255 | ||||||
chr11:70405529
|
T | A | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-1+168T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405529 | ||||||
chr11:70405552
|
C | G | 4 | a0002c0004t0004g0020a0002c0004t0004g0100a0002c0004t0004g0101others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+191C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405552 | ||||||
chr11:70405615
|
G | T | 1 | a0001c0003t0011g0057 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-1+254G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405615 | ||||||
chr11:70405706
|
T | C | 90 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(87): Show | 112 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-1+345T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405706 | ||||||
chr11:70405861
|
A | T | 1 | a0001c0003t0006g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-1+500A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405861 | ||||||
chr11:70405906
|
G | A | 1 | a0001c0003t0006g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-1+545G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405906 | ||||||
chr11:70405945
|
G | A | 8 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0007g0015others(5): Show | 9 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+584G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405945 | ||||||
chr11:70405984
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-1+623G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405984 | ||||||
chr11:70406103
|
C | A | 1 | a0001c0001t0021g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-1+742C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406103 | ||||||
chr11:70406173
|
G | T | 2 | a0001c0001t0021g0232a0001c0011t0012g0074 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-1+812G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406173 | ||||||
chr11:70406201
|
C | T | 3 | a0001c0001t0022g0238a0001c0006t0012g0075a0001c0006t0012g0076 | 3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-1+840C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406201 | ||||||
chr11:70406293
|
A | G | 8 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0007g0015others(5): Show | 9 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+932A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406293 | ||||||
chr11:70406345
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1-953C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406345 | ||||||
chr11:70406514
|
A | G | 2 | a0001c0001t0021g0232a0001c0011t0012g0074 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1-784A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406514 | ||||||
chr11:70406521
|
GA | G | 13 | a0001c0001t0001g0116a0001c0001t0001g0201a0001c0001t0001g0202others(10): Show | 16 | HG02145.hp1 HG02258.hp1 HG03225.hp1 others(13): Show |
intron_variant | MODIFIER | c.1-762delA | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr11 | 70406521 | |||||
chr11:70406682
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1-616G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406682 | ||||||
chr11:70406839
|
C | T | 3 | a0001c0001t0022g0238a0001c0006t0012g0075a0001c0006t0012g0076 | 3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1-459C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406839 | ||||||
chr11:70406947
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1-351G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406947 | ||||||
chr11:70407004
|
T | C | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1-294T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70407004 | ||||||
chr11:70407015
|
CT | C | 3 | a0001c0001t0014g0237a0001c0001t0014g0239a0001c0001t0017g0236 | 3 | HG02451.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1-277delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr11 | 70407015 | |||||
chr11:70407084
|
G | T | 1 | a0001c0001t0001g0039 | 2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1-214G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70407084 | ||||||
chr11:70407283
|
C | T | 36 | a0001c0001t0014g0237a0001c0001t0014g0239a0001c0001t0017g0236others(33): Show | 47 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1-15C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70407283 | ||||||
chr11:70407394
|
G | A | 1 | a0001c0001t0035g0148 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.87+10G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/17 | chr11 | 70407394 | ||||||
chr11:70407480
|
T | C | 132 | a0001c0001t0001g0099a0001c0001t0001g0128a0001c0001t0003g0010others(129): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.88-38T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/17 | chr11 | 70407480 | ||||||
chr11:70407482
|
C | A | 1 | a0001c0001t0017g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.88-36C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/17 | chr11 | 70407482 | ||||||
chr11:70407660
|
A | G | 2 | a0001c0001t0021g0232a0001c0011t0012g0074 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.161+69A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407660 | ||||||
chr11:70407805
|
G | T | 1 | a0001c0001t0021g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.161+214G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407805 | ||||||
chr11:70407851
|
A | C | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161+260A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407851 | ||||||
chr11:70407868
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161+277G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407868 | ||||||
chr11:70407884
|
G | T | 1 | a0001c0001t0001g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.161+293G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407884 | ||||||
chr11:70407950
|
T | C | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161+359T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407950 | ||||||
chr11:70408050
|
G | A | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161+459G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408050 | ||||||
chr11:70408082
|
G | C | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161+491G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408082 | ||||||
chr11:70408264
|
C | G | 1 | a0002c0004t0004g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.161+673C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408264 | ||||||
chr11:70408278
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.161+687G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408278 | ||||||
chr11:70408380
|
G | T | 5 | a0001c0001t0021g0232a0001c0001t0022g0238a0001c0006t0012g0075others(2): Show | 5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+789G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408380 | ||||||
chr11:70408457
|
G | C | 1 | a0001c0001t0003g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.161+866G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408457 | ||||||
chr11:70408462
|
A | G | 2 | a0001c0001t0003g0045a0001c0001t0003g0046 | 2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.161+871A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408462 | ||||||
chr11:70408690
|
G | A | 3 | a0001c0001t0022g0238a0001c0006t0012g0075a0001c0006t0012g0076 | 3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.161+1099G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408690 | ||||||
chr11:70408775
|
C | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.162-1056C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408775 | ||||||
chr11:70408784
|
G | A | 129 | a0001c0001t0001g0099a0001c0001t0003g0010a0001c0001t0003g0013others(126): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.162-1047G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408784 | ||||||
chr11:70409069
|
G | T | 24 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(21): Show | 33 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-762G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70409069 | ||||||
chr11:70409217
|
G | T | 2 | a0001c0001t0001g0038a0001c0001t0002g0199 | 3 | NA18994.hp2 NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.162-614G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70409217 | ||||||
chr11:70409624
|
C | T | 1 | a0001c0003t0008g0067 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162-207C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70409624 | ||||||
chr11:70410029
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.291+69C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410029 | ||||||
chr11:70410078
|
G | A | 1 | a0001c0001t0022g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.291+118G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410078 | ||||||
chr11:70410371
|
C | T | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.291+411C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410371 | ||||||
chr11:70410437
|
C | T | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.291+477C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410437 | ||||||
chr11:70410451
|
G | A | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+491G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410451 | ||||||
chr11:70410539
|
C | T | 4 | a0001c0002t0001g0019a0001c0002t0001g0088a0001c0002t0001g0098others(1): Show | 5 | HG01884.hp1 HG02055.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+579C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410539 | ||||||
chr11:70410545
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.291+585C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410545 | ||||||
chr11:70410840
|
C | T | 2 | a0001c0006t0012g0075a0001c0006t0012g0076 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.291+880C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410840 | ||||||
chr11:70410882
|
G | A | 3 | a0001c0001t0022g0238a0001c0006t0012g0075a0001c0006t0012g0076 | 3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.291+922G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410882 | ||||||
chr11:70410913
|
A | C | 45 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(42): Show | 58 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.291+953A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410913 | ||||||
chr11:70411004
|
T | C | 1 | a0001c0001t0034g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.291+1044T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411004 | ||||||
chr11:70411184
|
A | G | 26 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(23): Show | 35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.291+1224A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411184 | ||||||
chr11:70411185
|
A | AGTGCACA others(143): Show |
1 | a0001c0001t0022g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.291+1273_291+1274i others(152): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70411185 | |||||
chr11:70411185
|
A | T | 26 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(23): Show | 35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.291+1225A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411185 | ||||||
chr11:70411185
|
AGTGCACA others(43): Show |
A | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291+1399_291+1448d others(52): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70411185 | |||||
chr11:70411234
|
G | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(50): Show | 66 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.291+1274G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411234 | ||||||
chr11:70411274
|
C | T | 1 | a0001c0002t0002g0127 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.291+1314C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411274 | ||||||
chr11:70411279
|
G | A | 4 | a0001c0002t0002g0102a0001c0002t0002g0210a0001c0002t0009g0119others(1): Show | 4 | HG02080.hp1 NA18950.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1319G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411279 | ||||||
chr11:70411328
|
C | T | 2 | a0001c0001t0007g0080a0001c0001t0007g0081 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.291+1368C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411328 | ||||||
chr11:70411360
|
TGTGTTCA others(41): Show |
T | 1 | a0001c0001t0001g0128 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.291+1449_291+1496d others(50): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70411360 | |||||
chr11:70411408
|
C | CATGTGTT others(95): Show |
1 | a0001c0001t0034g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.291+1448_291+1449i others(104): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411408 | ||||||
chr11:70411408
|
C | CATGTGTT others(195): Show |
1 | a0002c0004t0002g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.291+1448_291+1449i others(204): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411408 | ||||||
chr11:70411408
|
C | CATGTGTT others(145): Show |
4 | a0001c0001t0021g0232a0001c0006t0012g0075a0001c0006t0012g0076others(1): Show | 4 | HG03453.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1448_291+1449i others(154): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411408 | ||||||
chr11:70411408
|
C | CATGTGTT others(195): Show |
24 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(21): Show | 33 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.291+1448_291+1449i others(204): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411408 | ||||||
chr11:70411441
|
C | T | 1 | a0001c0010t0002g0205 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.291+1481C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411441 | ||||||
chr11:70411503
|
A | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+1543A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411503 | ||||||
chr11:70411563
|
A | G | 142 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(139): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.291+1603A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411563 | ||||||
chr11:70411632
|
G | A | 2 | a0001c0006t0012g0075a0001c0006t0012g0076 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.291+1672G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411632 | ||||||
chr11:70411669
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.291+1709C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411669 | ||||||
chr11:70411689
|
C | T | 1 | a0001c0003t0019g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.291+1729C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411689 | ||||||
chr11:70411770
|
C | T | 1 | a0001c0002t0002g0018 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.291+1810C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411770 | ||||||
chr11:70411799
|
C | A | 4 | a0002c0004t0004g0020a0002c0004t0004g0100a0002c0004t0004g0101others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1839C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411799 | ||||||
chr11:70411890
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.291+1930G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411890 | ||||||
chr11:70411907
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.291+1947C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411907 | ||||||
chr11:70411942
|
C | G | 1 | a0001c0001t0023g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.291+1982C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411942 | ||||||
chr11:70411942
|
C | T | 1 | a0001c0003t0005g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.291+1982C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411942 | ||||||
chr11:70411943
|
C | A | 1 | a0001c0001t0034g0220 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.291+1983C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411943 | ||||||
chr11:70411944
|
C | G | 2 | a0001c0001t0021g0232a0001c0001t0022g0238 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.291+1984C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411944 | ||||||
chr11:70412005
|
C | T | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.291+2045C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412005 | ||||||
chr11:70412035
|
G | A | 1 | a0001c0002t0002g0218 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.291+2075G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412035 | ||||||
chr11:70412038
|
TC | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0013 | 5 | HG02145.hp1 HG02258.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+2080delC | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70412038 | |||||
chr11:70412073
|
T | C | 33 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(30): Show | 42 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.291+2113T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412073 | ||||||
chr11:70412126
|
C | T | 32 | a0001c0001t0001g0103a0001c0001t0003g0010a0001c0001t0003g0013others(29): Show | 41 | HG00438.hp1 HG01884.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.291+2166C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412126 | ||||||
chr11:70412162
|
G | C | 32 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(29): Show | 41 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.291+2202G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412162 | ||||||
chr11:70412340
|
C | T | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.292-2202C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412340 | ||||||
chr11:70412430
|
A | T | 1 | a0001c0002t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.292-2112A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412430 | ||||||
chr11:70412432
|
A | T | 1 | a0001c0002t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.292-2110A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412432 | ||||||
chr11:70412436
|
A | C | 1 | a0002c0004t0002g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.292-2106A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412436 | ||||||
chr11:70412503
|
CTA | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0153a0001c0001t0001g0198 | 3 | HG02165.hp2 NA18977.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.292-2038_292-2037d others(4): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412503 | ||||||
chr11:70412904
|
T | C | 1 | a0001c0002t0002g0120 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.292-1638T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412904 | ||||||
chr11:70412923
|
C | T | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.292-1619C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412923 | ||||||
chr11:70413011
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG00609.hp1 NA18942.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1531C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413011 | ||||||
chr11:70413102
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.292-1440G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413102 | ||||||
chr11:70413176
|
C | T | 1 | a0001c0003t0005g0066 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.292-1366C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413176 | ||||||
chr11:70413207
|
G | A | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.292-1335G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413207 | ||||||
chr11:70413914
|
G | A | 1 | a0001c0001t0023g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292-628G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413914 | ||||||
chr11:70413922
|
C | CCA | 5 | a0001c0001t0021g0232a0001c0001t0022g0238a0001c0006t0012g0075others(2): Show | 5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-617_292-616dup others(2): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70413922 | |||||
chr11:70414198
|
A | C | 1 | a0001c0003t0028g0144 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.292-344A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414198 | ||||||
chr11:70414291
|
G | A | 1 | a0001c0003t0006g0137 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.292-251G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414291 | ||||||
chr11:70414339
|
T | C | 146 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(143): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.292-203T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414339 | ||||||
chr11:70414395
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.292-147G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414395 | ||||||
chr11:70414437
|
C | G | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.292-105C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414437 | ||||||
chr11:70414466
|
C | T | 1 | a0001c0001t0013g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.292-76C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414466 | ||||||
chr11:70414492
|
C | T | 17 | a0001c0003t0005g0006a0001c0003t0005g0014a0001c0003t0005g0056others(14): Show | 26 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.292-50C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414492 | ||||||
chr11:70414503
|
T | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(47): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.292-39T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414503 | ||||||
chr11:70414664
|
G | A | 1 | a0001c0003t0005g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.402+12G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414664 | ||||||
chr11:70414727
|
G | T | 5 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG00597.hp2 HG00609.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+75G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414727 | ||||||
chr11:70414839
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.402+187C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414839 | ||||||
chr11:70414878
|
C | T | 1 | a0001c0003t0006g0137 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.402+226C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414878 | ||||||
chr11:70414955
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0038others(8): Show | 22 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.402+303A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414955 | ||||||
chr11:70415037
|
T | C | 25 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(22): Show | 34 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.402+385T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415037 | ||||||
chr11:70415149
|
G | C | 1 | a0001c0001t0022g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.402+497G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415149 | ||||||
chr11:70415227
|
T | G | 1 | a0001c0003t0005g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.403-436T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415227 | ||||||
chr11:70415298
|
G | C | 25 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(22): Show | 34 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.403-365G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415298 | ||||||
chr11:70415430
|
A | G | 50 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(47): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.403-233A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415430 | ||||||
chr11:70415487
|
T | G | 1 | a0001c0001t0014g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.403-176T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415487 | ||||||
chr11:70415619
|
A | G | 1 | a0004c0012t0001g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.403-44A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415619 | ||||||
chr11:70415622
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.403-41G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415622 | ||||||
chr11:70415725
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.457+8G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70415725 | ||||||
chr11:70415727
|
G | A | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.457+10G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70415727 | ||||||
chr11:70415793
|
T | TC | 5 | a0001c0001t0001g0158a0001c0001t0003g0051a0001c0001t0007g0112others(2): Show | 5 | HG00733.hp1 HG02135.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+80dupC | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 70415793 | |||||
chr11:70415999
|
C | T | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+282C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70415999 | ||||||
chr11:70416109
|
ATTC | A | 62 | a0001c0001t0001g0099a0001c0001t0003g0047a0001c0001t0003g0048others(59): Show | 73 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.457+395_457+397del others(3): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 70416109 | |||||
chr11:70416203
|
G | T | 1 | a0001c0001t0001g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.457+486G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416203 | ||||||
chr11:70416229
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.457+512T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416229 | ||||||
chr11:70416245
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.457+528G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416245 | ||||||
chr11:70416273
|
T | G | 53 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(50): Show | 70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.457+556T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416273 | ||||||
chr11:70416545
|
C | A | 25 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(22): Show | 34 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.458-468C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416545 | ||||||
chr11:70416635
|
G | A | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.458-378G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416635 | ||||||
chr11:70416827
|
G | A | 1 | a0001c0003t0005g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.458-186G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416827 | ||||||
chr11:70416868
|
C | A | 4 | a0001c0001t0021g0232a0001c0001t0022g0238a0001c0006t0012g0075others(1): Show | 4 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-145C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416868 | ||||||
chr11:70416882
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.458-131T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416882 | ||||||
chr11:70417245
|
G | A | 61 | a0001c0001t0001g0099a0001c0001t0003g0047a0001c0001t0003g0048others(58): Show | 72 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.568+122G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417245 | ||||||
chr11:70417409
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.568+286C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417409 | ||||||
chr11:70417428
|
G | A | 3 | a0001c0001t0007g0015a0001c0001t0007g0073a0001c0001t0015g0015 | 3 | HG02055.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.568+305G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417428 | ||||||
chr11:70417491
|
G | A | 8 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0051others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+368G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417491 | ||||||
chr11:70417610
|
T | C | 34 | a0001c0001t0001g0155a0001c0003t0001g0140a0001c0003t0005g0006others(31): Show | 45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.568+487T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417610 | ||||||
chr11:70417620
|
C | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.568+497C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417620 | ||||||
chr11:70417684
|
C | T | 1 | a0002c0004t0001g0078 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.568+561C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417684 | ||||||
chr11:70417685
|
G | A | 1 | a0001c0006t0012g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.568+562G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417685 | ||||||
chr11:70417716
|
G | T | 8 | a0002c0004t0001g0078a0002c0004t0004g0004a0002c0004t0004g0042others(5): Show | 14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.568+593G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417716 | ||||||
chr11:70417736
|
T | TCGCCCTG others(10): Show |
1 | a0001c0001t0001g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.568+615_568+631dup others(17): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70417736 | |||||
chr11:70417801
|
T | C | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.568+678T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417801 | ||||||
chr11:70418121
|
CA | C | 42 | a0001c0001t0001g0155a0001c0001t0001g0183a0001c0001t0001g0184others(39): Show | 53 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.568+1012delA | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70418121 | |||||
chr11:70418259
|
T | G | 132 | a0001c0001t0001g0099a0001c0001t0001g0128a0001c0001t0001g0155others(129): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.568+1136T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418259 | ||||||
chr11:70418289
|
G | A | 1 | a0001c0003t0006g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.568+1166G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418289 | ||||||
chr11:70418355
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.568+1232C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418355 | ||||||
chr11:70418507
|
C | T | 1 | a0001c0001t0017g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.569-1239C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418507 | ||||||
chr11:70418560
|
A | G | 2 | a0001c0006t0012g0075a0001c0006t0012g0076 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569-1186A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418560 | ||||||
chr11:70418584
|
A | G | 35 | a0001c0001t0001g0155a0001c0003t0001g0140a0001c0003t0005g0006others(32): Show | 46 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.569-1162A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418584 | ||||||
chr11:70418714
|
C | T | 1 | a0001c0003t0006g0143 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.569-1032C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418714 | ||||||
chr11:70418736
|
G | A | 8 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0051others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-1010G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418736 | ||||||
chr11:70418779
|
C | CT | 11 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0051others(8): Show | 11 | HG02257.hp1 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.569-951dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70418779 | |||||
chr11:70418779
|
CT | C | 9 | a0001c0001t0001g0109a0001c0001t0001g0159a0001c0001t0001g0160others(6): Show | 9 | HG00639.hp2 HG01517.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.569-951delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70418779 | |||||
chr11:70418801
|
G | A | 1 | a0001c0005t0002g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.569-945G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418801 | ||||||
chr11:70418840
|
G | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0152a0001c0001t0001g0161others(3): Show | 6 | HG00639.hp1 HG01106.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-906G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418840 | ||||||
chr11:70418869
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.569-877C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418869 | ||||||
chr11:70418908
|
C | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.569-838C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418908 | ||||||
chr11:70419053
|
G | A | 1 | a0001c0002t0002g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.569-693G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419053 | ||||||
chr11:70419114
|
CT | C | 120 | a0001c0001t0001g0108a0001c0001t0001g0155a0001c0001t0001g0158others(117): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.569-619delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70419114 | |||||
chr11:70419132
|
T | C | 4 | a0001c0001t0007g0016a0001c0001t0007g0080a0001c0001t0007g0081others(1): Show | 5 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-614T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419132 | ||||||
chr11:70419146
|
T | G | 13 | a0001c0002t0001g0090a0001c0002t0001g0092a0001c0002t0001g0094others(10): Show | 14 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.569-600T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419146 | ||||||
chr11:70419330
|
A | G | 33 | a0001c0001t0001g0155a0001c0003t0001g0140a0001c0003t0005g0006others(30): Show | 44 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.569-416A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419330 | ||||||
chr11:70419361
|
C | A | 2 | a0001c0006t0012g0075a0001c0006t0012g0076 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569-385C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419361 | ||||||
chr11:70419488
|
C | A | 34 | a0001c0001t0001g0155a0001c0003t0001g0140a0001c0003t0005g0006others(31): Show | 45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.569-258C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419488 | ||||||
chr11:70419572
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.569-174T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419572 | ||||||
chr11:70419938
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.679+82G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70419938 | ||||||
chr11:70420012
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.679+156C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420012 | ||||||
chr11:70420100
|
G | A | 1 | a0001c0002t0002g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.679+244G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420100 | ||||||
chr11:70420140
|
G | A | 33 | a0001c0001t0001g0155a0001c0003t0001g0140a0001c0003t0005g0006others(30): Show | 44 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.680-260G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420140 | ||||||
chr11:70420151
|
G | T | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.680-249G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420151 | ||||||
chr11:70420157
|
G | A | 1 | a0001c0001t0001g0027 | 2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.680-243G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420157 | ||||||
chr11:70420221
|
T | G | 1 | a0001c0001t0013g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.680-179T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420221 | ||||||
chr11:70420235
|
A | G | 10 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0007g0015others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.680-165A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420235 | ||||||
chr11:70420336
|
A | G | 23 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0051others(20): Show | 29 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.680-64A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420336 | ||||||
chr11:70420520
|
C | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.790+10C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420520 | ||||||
chr11:70420621
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.790+111C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420621 | ||||||
chr11:70420736
|
C | T | 1 | a0001c0002t0002g0125 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.790+226C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420736 | ||||||
chr11:70420752
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0186a0001c0001t0024g0216 | 3 | HG00735.hp2 HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.790+242C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420752 | ||||||
chr11:70420772
|
G | A | 1 | a0001c0002t0002g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.790+262G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420772 | ||||||
chr11:70420817
|
G | C | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.790+307G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420817 | ||||||
chr11:70420835
|
G | A | 1 | a0001c0002t0002g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.790+325G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420835 | ||||||
chr11:70420920
|
A | G | 34 | a0001c0001t0001g0155a0001c0003t0001g0140a0001c0003t0005g0006others(31): Show | 45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.790+410A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420920 | ||||||
chr11:70420987
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.790+477G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420987 | ||||||
chr11:70421063
|
C | T | 3 | a0001c0002t0002g0077a0001c0002t0002g0218a0001c0002t0002g0219 | 3 | HG02647.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.791-407C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70421063 | ||||||
chr11:70421113
|
A | G | 26 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(23): Show | 35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.791-357A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70421113 | ||||||
chr11:70421141
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.791-329A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70421141 | ||||||
chr11:70421164
|
G | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.791-306G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70421164 | ||||||
chr11:70421242
|
G | GT | 34 | a0001c0001t0001g0155a0001c0003t0001g0140a0001c0003t0005g0006others(31): Show | 45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.791-226dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 70421242 | |||||
chr11:70421748
|
C | G | 1 | a0001c0001t0001g0160 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.901+168C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70421748 | ||||||
chr11:70421823
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.901+243G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70421823 | ||||||
chr11:70421877
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.901+297G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70421877 | ||||||
chr11:70422035
|
C | T | 1 | a0001c0001t0007g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.901+455C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422035 | ||||||
chr11:70422086
|
G | A | 1 | a0001c0003t0005g0066 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.901+506G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422086 | ||||||
chr11:70422368
|
G | A | 7 | a0001c0002t0001g0003a0001c0002t0002g0003a0001c0002t0002g0226others(4): Show | 11 | HG00280.hp1 HG00733.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.902-572G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422368 | ||||||
chr11:70422704
|
C | T | 1 | a0001c0001t0007g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.902-236C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422704 | ||||||
chr11:70422716
|
A | T | 1 | a0001c0001t0007g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.902-224A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422716 | ||||||
chr11:70422724
|
GC | G | 3 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0013g0049 | 6 | HG02145.hp1 HG02258.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.902-212delC | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr11 | 70422724 | |||||
chr11:70422804
|
C | T | 32 | a0001c0003t0001g0140a0001c0003t0005g0006a0001c0003t0005g0014others(29): Show | 43 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.902-136C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422804 | ||||||
chr11:70422882
|
G | A | 1 | a0001c0003t0005g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.902-58G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422882 | ||||||
chr11:70423051
|
G | T | 1 | a0001c0001t0007g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.957+56G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423051 | ||||||
chr11:70423080
|
C | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0211a0001c0001t0001g0214others(2): Show | 7 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.957+85C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423080 | ||||||
chr11:70423109
|
G | A | 1 | a0001c0002t0002g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.957+114G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423109 | ||||||
chr11:70423128
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.957+133T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423128 | ||||||
chr11:70423209
|
T | A | 2 | a0001c0006t0012g0075a0001c0006t0012g0076 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.957+214T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423209 | ||||||
chr11:70423370
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0030g0212 | 2 | NA19001.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.957+375T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423370 | ||||||
chr11:70423372
|
C | G | 2 | a0001c0001t0001g0165a0001c0001t0030g0212 | 2 | NA19001.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.957+377C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423372 | ||||||
chr11:70423451
|
A | G | 1 | a0001c0003t0006g0143 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.957+456A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423451 | ||||||
chr11:70423538
|
G | A | 1 | a0001c0001t0022g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.957+543G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423538 | ||||||
chr11:70423670
|
G | A | 3 | a0001c0002t0002g0102a0001c0002t0002g0210a0001c0002t0009g0119 | 3 | NA18950.hp1 NA18977.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.957+675G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423670 | ||||||
chr11:70423671
|
T | G | 62 | a0001c0001t0001g0099a0001c0001t0003g0047a0001c0001t0003g0048others(59): Show | 73 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.957+676T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423671 | ||||||
chr11:70423781
|
G | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 7 | HG00738.hp1 HG01346.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.957+786G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423781 | ||||||
chr11:70423783
|
C | T | 3 | a0001c0003t0006g0022a0001c0003t0006g0129a0001c0003t0036g0130 | 4 | HG02083.hp2 NA18953.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+788C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423783 | ||||||
chr11:70423816
|
C | T | 1 | a0001c0002t0002g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.957+821C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423816 | ||||||
chr11:70424037
|
G | A | 3 | a0001c0001t0007g0015a0001c0001t0007g0073a0001c0001t0015g0015 | 3 | HG02055.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.957+1042G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424037 | ||||||
chr11:70424114
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0016g0029a0001c0001t0016g0169 | 3 | HG01496.hp1 HG02109.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.957+1119G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424114 | ||||||
chr11:70424121
|
T | G | 5 | a0001c0001t0021g0232a0001c0001t0022g0238a0001c0006t0012g0075others(2): Show | 5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+1126T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424121 | ||||||
chr11:70424356
|
G | A | 1 | a0001c0003t0019g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.958-976G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424356 | ||||||
chr11:70424360
|
G | A | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.958-972G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424360 | ||||||
chr11:70424496
|
A | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(249): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.958-836A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424496 | ||||||
chr11:70424538
|
A | G | 34 | a0001c0001t0001g0155a0001c0003t0001g0140a0001c0003t0005g0006others(31): Show | 45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.958-794A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424538 | ||||||
chr11:70424737
|
G | T | 2 | a0001c0001t0021g0232a0001c0001t0022g0238 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.958-595G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424737 | ||||||
chr11:70424859
|
C | A | 1 | a0002c0004t0004g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.958-473C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424859 | ||||||
chr11:70424892
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.958-440G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424892 | ||||||
chr11:70425175
|
T | G | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.958-157T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70425175 | ||||||
chr11:70425522
|
G | A | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1027+121G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425522 | ||||||
chr11:70425590
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1027+189C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425590 | ||||||
chr11:70425598
|
C | T | 3 | a0001c0002t0002g0077a0001c0002t0002g0218a0001c0002t0002g0219 | 3 | HG02647.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1027+197C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425598 | ||||||
chr11:70425614
|
C | T | 4 | a0002c0004t0004g0020a0002c0004t0004g0100a0002c0004t0004g0101others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027+213C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425614 | ||||||
chr11:70425821
|
G | A | 33 | a0001c0001t0001g0155a0001c0003t0001g0140a0001c0003t0005g0006others(30): Show | 44 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1027+420G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425821 | ||||||
chr11:70425936
|
A | G | 37 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0223others(34): Show | 49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1027+535A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425936 | ||||||
chr11:70426164
|
T | C | 2 | a0001c0006t0012g0075a0001c0006t0012g0076 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1027+763T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426164 | ||||||
chr11:70426223
|
C | T | 31 | a0001c0001t0001g0155a0001c0003t0005g0006a0001c0003t0005g0014others(28): Show | 42 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1027+822C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426223 | ||||||
chr11:70426302
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1027+901T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426302 | ||||||
chr11:70426392
|
C | T | 1 | a0001c0003t0006g0022 | 2 | HG02083.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1027+991C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426392 | ||||||
chr11:70426406
|
G | A | 1 | a0001c0002t0002g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1027+1005G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426406 | ||||||
chr11:70426410
|
C | CA | 14 | a0001c0001t0001g0110a0001c0001t0001g0192a0001c0001t0003g0051others(11): Show | 14 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.1027+1025dupA | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70426410 | |||||
chr11:70426413
|
A | G | 1 | a0001c0001t0013g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1027+1012A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426413 | ||||||
chr11:70426646
|
G | A | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1027+1245G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426646 | ||||||
chr11:70426647
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(251): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1027+1246G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426647 | ||||||
chr11:70426668
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0035others(7): Show | 15 | HG00544.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1027+1267C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426668 | ||||||
chr11:70426781
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1027+1380T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426781 | ||||||
chr11:70426785
|
A | G | 1 | a0001c0002t0002g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1027+1384A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426785 | ||||||
chr11:70426801
|
C | T | 1 | a0001c0001t0023g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1027+1400C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426801 | ||||||
chr11:70426822
|
G | T | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1027+1421G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426822 | ||||||
chr11:70426895
|
C | T | 34 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0223others(31): Show | 46 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1027+1494C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426895 | ||||||
chr11:70427030
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1027+1629A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427030 | ||||||
chr11:70427065
|
C | T | 5 | a0001c0001t0021g0232a0001c0001t0022g0238a0001c0006t0012g0075others(2): Show | 5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027+1664C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427065 | ||||||
chr11:70427087
|
T | C | 133 | a0001c0001t0001g0037a0001c0001t0001g0099a0001c0001t0001g0155others(130): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1027+1686T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427087 | ||||||
chr11:70427090
|
C | T | 1 | a0001c0003t0005g0066 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1027+1689C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427090 | ||||||
chr11:70427150
|
G | C | 1 | a0001c0001t0003g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1027+1749G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427150 | ||||||
chr11:70427195
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0030g0212 | 2 | NA19001.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1027+1794C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427195 | ||||||
chr11:70427342
|
T | G | 2 | a0001c0001t0001g0167a0001c0001t0025g0166 | 2 | HG01515.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1028-1709T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427342 | ||||||
chr11:70427395
|
T | G | 1 | a0001c0001t0003g0013 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1028-1656T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427395 | ||||||
chr11:70427436
|
T | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0178 | 3 | HG01981.hp1 NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1028-1615T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427436 | ||||||
chr11:70427484
|
C | T | 1 | a0001c0001t0013g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1028-1567C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427484 | ||||||
chr11:70427506
|
G | A | 8 | a0002c0004t0001g0078a0002c0004t0004g0004a0002c0004t0004g0042others(5): Show | 14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1028-1545G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427506 | ||||||
chr11:70427524
|
G | T | 5 | a0001c0001t0021g0232a0001c0001t0022g0238a0001c0006t0012g0075others(2): Show | 5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-1527G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427524 | ||||||
chr11:70427654
|
C | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1028-1397C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427654 | ||||||
chr11:70427665
|
C | T | 3 | a0001c0002t0001g0092a0001c0002t0001g0094a0001c0002t0032g0093 | 3 | HG01074.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1028-1386C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427665 | ||||||
chr11:70427800
|
A | T | 1 | a0002c0004t0002g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1028-1251A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427800 | ||||||
chr11:70427893
|
AT | A | 35 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0223others(32): Show | 47 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1028-1154delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70427893 | |||||
chr11:70428042
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1028-1009A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428042 | ||||||
chr11:70428085
|
G | T | 41 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0223others(38): Show | 53 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1028-966G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428085 | ||||||
chr11:70428120
|
G | A | 1 | a0002c0004t0002g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1028-931G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428120 | ||||||
chr11:70428153
|
C | CT | 4 | a0001c0001t0001g0011a0001c0001t0001g0229a0001c0001t0002g0199others(1): Show | 6 | HG00733.hp2 HG01952.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1028-867dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | |||||
chr11:70428153
|
CT | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(81): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1028-867delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | |||||
chr11:70428153
|
CTT | C | 48 | a0001c0001t0001g0099a0001c0001t0001g0111a0001c0001t0001g0132others(45): Show | 61 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.1028-868_1028-867d others(4): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | |||||
chr11:70428153
|
CTTT | C | 38 | a0001c0001t0001g0037a0001c0001t0001g0128a0001c0001t0001g0155others(35): Show | 46 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1028-869_1028-867d others(5): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | |||||
chr11:70428153
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1028-876_1028-867d others(12): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | |||||
chr11:70428153
|
CTTTTTTT others(4): Show |
C | 25 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(22): Show | 34 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1028-877_1028-867d others(13): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | |||||
chr11:70428184
|
T | G | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1028-867T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428184 | ||||||
chr11:70428290
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1028-761C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428290 | ||||||
chr11:70428293
|
G | C | 2 | a0001c0006t0012g0075a0001c0006t0012g0076 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1028-758G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428293 | ||||||
chr11:70428385
|
T | C | 35 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0223others(32): Show | 47 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1028-666T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428385 | ||||||
chr11:70428406
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1028-645C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428406 | ||||||
chr11:70428468
|
T | C | 1 | a0001c0001t0022g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1028-583T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428468 | ||||||
chr11:70428636
|
A | T | 35 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0223others(32): Show | 47 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1028-415A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428636 | ||||||
chr11:70428660
|
G | A | 1 | a0001c0001t0014g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1028-391G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428660 | ||||||
chr11:70428794
|
C | T | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1028-257C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428794 | ||||||
chr11:70428795
|
G | A | 1 | a0001c0001t0022g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1028-256G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428795 | ||||||
chr11:70428847
|
C | T | 1 | a0001c0001t0002g0175 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1028-204C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428847 | ||||||
chr11:70428873
|
T | C | 36 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0223others(33): Show | 48 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1028-178T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428873 | ||||||
chr11:70429203
|
A | G | 8 | a0002c0004t0001g0078a0002c0004t0004g0004a0002c0004t0004g0042others(5): Show | 14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1176+4A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429203 | ||||||
chr11:70429409
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1176+210C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429409 | ||||||
chr11:70429410
|
G | A | 1 | a0001c0001t0026g0118 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1176+211G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429410 | ||||||
chr11:70429417
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1176+218G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429417 | ||||||
chr11:70429438
|
C | T | 13 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(10): Show | 15 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1176+239C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429438 | ||||||
chr11:70429528
|
A | G | 1 | a0001c0002t0032g0093 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1176+329A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429528 | ||||||
chr11:70429532
|
G | A | 8 | a0002c0004t0001g0078a0002c0004t0004g0004a0002c0004t0004g0042others(5): Show | 14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1176+333G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429532 | ||||||
chr11:70429538
|
C | T | 1 | a0001c0001t0015g0097 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1176+339C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429538 | ||||||
chr11:70429668
|
G | A | 63 | a0001c0001t0001g0099a0001c0001t0003g0047a0001c0001t0003g0048others(60): Show | 74 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1176+469G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429668 | ||||||
chr11:70429702
|
C | T | 1 | a0001c0002t0009g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1176+503C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429702 | ||||||
chr11:70429793
|
C | T | 52 | a0001c0002t0001g0003a0001c0002t0001g0019a0001c0002t0001g0040others(49): Show | 62 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1176+594C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429793 | ||||||
chr11:70429826
|
A | AC | 6 | a0001c0001t0001g0026a0001c0001t0001g0152a0001c0001t0001g0161others(3): Show | 6 | HG00639.hp1 HG01106.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1176+627_1176+628i others(3): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429826 | ||||||
chr11:70429869
|
G | T | 34 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0223others(31): Show | 46 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1176+670G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429869 | ||||||
chr11:70429874
|
G | A | 1 | a0002c0004t0004g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1176+675G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429874 | ||||||
chr11:70429903
|
A | G | 41 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0001g0223others(38): Show | 53 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1176+704A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429903 | ||||||
chr11:70430089
|
C | T | 2 | a0001c0001t0021g0232a0001c0001t0022g0238 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1176+890C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430089 | ||||||
chr11:70430090
|
G | A | 1 | a0001c0001t0007g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1176+891G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430090 | ||||||
chr11:70430157
|
C | T | 8 | a0002c0004t0001g0078a0002c0004t0004g0004a0002c0004t0004g0042others(5): Show | 14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1176+958C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430157 | ||||||
chr11:70430171
|
C | T | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1176+972C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430171 | ||||||
chr11:70430240
|
T | C | 40 | a0001c0001t0001g0037a0001c0001t0001g0223a0001c0001t0021g0232others(37): Show | 52 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1177-951T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430240 | ||||||
chr11:70430373
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1177-818T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430373 | ||||||
chr11:70430390
|
G | A | 36 | a0001c0001t0001g0037a0001c0001t0001g0223a0001c0001t0021g0232others(33): Show | 48 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1177-801G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430390 | ||||||
chr11:70430609
|
C | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0229 | 2 | HG02074.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1177-582C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430609 | ||||||
chr11:70430629
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1177-562G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430629 | ||||||
chr11:70430667
|
T | A | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1177-524T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430667 | ||||||
chr11:70430712
|
C | T | 52 | a0001c0002t0001g0003a0001c0002t0001g0019a0001c0002t0001g0040others(49): Show | 62 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1177-479C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430712 | ||||||
chr11:70430723
|
C | T | 13 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0145others(10): Show | 15 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1177-468C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430723 | ||||||
chr11:70430789
|
A | G | 4 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0083others(1): Show | 5 | HG01070.hp1 HG01071.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1177-402A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430789 | ||||||
chr11:70430880
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1177-311C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430880 | ||||||
chr11:70430885
|
C | T | 1 | a0001c0001t0014g0239 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1177-306C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430885 | ||||||
chr11:70430911
|
G | A | 1 | a0001c0001t0016g0169 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1177-280G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430911 | ||||||
chr11:70430948
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1177-243G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430948 | ||||||
chr11:70431312
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1266+32G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431312 | ||||||
chr11:70431366
|
G | A | 1 | a0001c0002t0020g0059 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1266+86G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431366 | ||||||
chr11:70431377
|
T | C | 1 | a0001c0002t0033g0123 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1266+97T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431377 | ||||||
chr11:70431411
|
G | A | 1 | a0001c0011t0012g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1266+131G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431411 | ||||||
chr11:70431536
|
C | G | 9 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0051others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266+256C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431536 | ||||||
chr11:70431681
|
C | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1266+401C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431681 | ||||||
chr11:70431793
|
C | T | 3 | a0001c0002t0002g0102a0001c0002t0002g0210a0001c0002t0009g0119 | 3 | NA18950.hp1 NA18977.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1266+513C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431793 | ||||||
chr11:70431983
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1266+703T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431983 | ||||||
chr11:70432081
|
G | A | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1266+801G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432081 | ||||||
chr11:70432144
|
A | G | 29 | a0001c0003t0005g0006a0001c0003t0005g0014a0001c0003t0005g0056others(26): Show | 40 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1266+864A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432144 | ||||||
chr11:70432145
|
C | T | 128 | a0001c0001t0001g0099a0001c0001t0003g0010a0001c0001t0003g0013others(125): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1266+865C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432145 | ||||||
chr11:70432271
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1267-830A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432271 | ||||||
chr11:70432280
|
C | T | 2 | a0001c0006t0012g0075a0001c0006t0012g0076 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1267-821C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432280 | ||||||
chr11:70432304
|
C | A | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1267-797C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432304 | ||||||
chr11:70432369
|
C | T | 1 | a0001c0001t0001g0039 | 2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1267-732C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432369 | ||||||
chr11:70432459
|
C | A | 64 | a0001c0001t0001g0099a0001c0001t0003g0047a0001c0001t0003g0048others(61): Show | 75 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1267-642C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432459 | ||||||
chr11:70432461
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1267-640G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432461 | ||||||
chr11:70432467
|
A | G | 31 | a0001c0003t0005g0006a0001c0003t0005g0014a0001c0003t0005g0056others(28): Show | 42 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1267-634A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432467 | ||||||
chr11:70432510
|
G | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-591G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432510 | ||||||
chr11:70432557
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0161a0001c0001t0002g0026 | 3 | HG02145.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1267-544G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432557 | ||||||
chr11:70432565
|
T | A | 1 | a0001c0003t0008g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1267-536T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432565 | ||||||
chr11:70432651
|
C | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-450C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432651 | ||||||
chr11:70432689
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1267-412A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432689 | ||||||
chr11:70432729
|
T | C | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-372T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432729 | ||||||
chr11:70432732
|
G | A | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-369G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432732 | ||||||
chr11:70432786
|
G | A | 1 | a0001c0003t0005g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1267-315G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432786 | ||||||
chr11:70432799
|
C | G | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-302C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432799 | ||||||
chr11:70432873
|
C | A | 1 | a0005c0008t0004g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1267-228C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432873 | ||||||
chr11:70432982
|
G | A | 23 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0051others(20): Show | 29 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1267-119G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432982 | ||||||
chr11:70432995
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1267-106C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432995 | ||||||
chr11:70433012
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1267-89C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70433012 | ||||||
chr11:70433359
|
G | T | 26 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(23): Show | 35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1444+81G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/17 | chr11 | 70433359 | ||||||
chr11:70433365
|
C | T | 1 | a0001c0009t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1444+87C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/17 | chr11 | 70433365 | ||||||
chr11:70433366
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1444+88G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/17 | chr11 | 70433366 | ||||||
chr11:70433521
|
G | A | 26 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(23): Show | 35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1445-126G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/17 | chr11 | 70433521 | ||||||
chr11:70433821
|
G | A | 61 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(58): Show | 81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1516+103G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70433821 | ||||||
chr11:70433832
|
T | C | 10 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0007g0015others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+114T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70433832 | ||||||
chr11:70433883
|
C | G | 1 | a0001c0002t0002g0228 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1516+165C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70433883 | ||||||
chr11:70433890
|
C | G | 1 | a0001c0006t0012g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1516+172C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70433890 | ||||||
chr11:70434136
|
A | G | 35 | a0001c0001t0021g0232a0001c0001t0022g0238a0001c0003t0005g0006others(32): Show | 46 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1516+418A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434136 | ||||||
chr11:70434168
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0177 | 2 | HG02027.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1516+450A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434168 | ||||||
chr11:70434206
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1516+488C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434206 | ||||||
chr11:70434216
|
G | A | 1 | a0001c0002t0002g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1516+498G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434216 | ||||||
chr11:70434255
|
G | A | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1516+537G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434255 | ||||||
chr11:70434297
|
C | T | 7 | a0001c0001t0001g0165a0001c0001t0001g0174a0001c0001t0001g0194others(4): Show | 7 | HG00597.hp2 HG00609.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1516+579C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434297 | ||||||
chr11:70434430
|
G | A | 1 | a0001c0002t0009g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1517-596G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434430 | ||||||
chr11:70434630
|
G | A | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1517-396G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434630 | ||||||
chr11:70434696
|
C | G | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1517-330C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434696 | ||||||
chr11:70434706
|
C | T | 10 | a0001c0001t0003g0045a0001c0001t0003g0046a0001c0001t0003g0051others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1517-320C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434706 | ||||||
chr11:70434708
|
C | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1517-318C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434708 | ||||||
chr11:70434787
|
G | A | 30 | a0001c0003t0005g0006a0001c0003t0005g0014a0001c0003t0005g0056others(27): Show | 41 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1517-239G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434787 | ||||||
chr11:70434886
|
G | A | 63 | a0001c0001t0001g0099a0001c0001t0003g0047a0001c0001t0003g0048others(60): Show | 74 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1517-140G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434886 | ||||||
chr11:70434895
|
C | T | 1 | a0001c0002t0002g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1517-131C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434895 | ||||||
chr11:70434900
|
G | T | 1 | a0001c0013t0013g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1517-126G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434900 | ||||||
chr11:70434901
|
T | C | 63 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0045others(60): Show | 83 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1517-125T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434901 | ||||||
chr11:70434977
|
C | T | 3 | a0001c0001t0014g0237a0001c0001t0014g0239a0001c0001t0017g0236 | 3 | HG02451.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1517-49C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434977 |