geneid | 2934 |
---|---|
ensemblid | ENSG00000148180.22 |
hgncid | 4620 |
symbol | GSN |
name | gelsolin |
refseq_nuc | NM_198252.3 |
refseq_prot | NP_937895.1 |
ensembl_nuc | ENST00000432226.7 |
ensembl_prot | ENSP00000404226.2 |
mane_status | MANE Select |
chr | chr9 |
start | 121268162 |
end | 121332842 |
strand | + |
ver | v1.2 |
region | chr9:121268162-121332842 |
region5000 | chr9:121263162-121337842 |
regionname0 | GSN_chr9_121268162_121332842 |
regionname5000 | GSN_chr9_121263162_121337842 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 731 | 242 | 58 | 52 | 98 | 13 | 20 | 71 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002 | 0/0 | 731 | 47 | 2 | 12 | 28 | 0 | 5 | 22 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0003 | 0/0 | 731 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0004 | 0/0 | 731 | 6 | 3 | 1 | 0 | 0 | 2 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0005 | 0/0 | 731 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0006 | 0/0 | 731 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0007 | 0/1 | 731 | 2 | 0 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0008 | 0/0 | 731 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0009 | 0/0 | 731 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0010 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0011 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0012 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0013 | 0/0 | 731 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0014 | 0/0 | 731 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0015 | 0/0 | 731 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0016 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2196 | 203 | 50 | 46 | 75 | 13 | 18 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0002 | 0/0 | 2196 | 40 | 2 | 11 | 23 | 0 | 4 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0003 | 0/0 | 2196 | 28 | 6 | 2 | 19 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0004 | 0/0 | 2196 | 8 | 0 | 3 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0005 | 0/0 | 2196 | 8 | 8 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0006 | 0/0 | 2196 | 6 | 3 | 1 | 0 | 0 | 2 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0007 | 0/0 | 2196 | 5 | 0 | 0 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0008 | 0/0 | 2196 | 3 | 2 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0009 | 0/0 | 2196 | 3 | 3 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0010 | 0/0 | 2196 | 2 | 1 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0011 | 0/0 | 2196 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0012 | 0/0 | 2196 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0013 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0014 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0015 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0016 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0017 | 0/0 | 2196 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0018 | 0/1 | 2196 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0019 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0020 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0021 | 0/0 | 2196 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0022 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0023 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
c0024 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 400 | 252 | 69 | 47 | 99 | 14 | 21 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
t0002 | 0/0 | 402 | 46 | 0 | 13 | 28 | 0 | 5 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
t0003 | 0/0 | 402 | 11 | 7 | 4 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
t0004 | 0/0 | 404 | 10 | 7 | 1 | 0 | 0 | 2 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
t0005 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
t0006 | 0/0 | 400 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
t0007 | 0/0 | 402 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0004 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0006 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0014 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0033 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2196 | 203 | 50 | 46 | 75 | 13 | 18 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0003 | 0/0 | 2196 | 28 | 6 | 2 | 19 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0004 | 0/0 | 2196 | 8 | 0 | 3 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0010 | 0/0 | 2196 | 2 | 1 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0023 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0002 | 0/0 | 2196 | 40 | 2 | 11 | 23 | 0 | 4 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0007 | 0/0 | 2196 | 5 | 0 | 0 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0014 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0015 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0003c0005 | 0/0 | 2196 | 8 | 8 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0004c0006 | 0/0 | 2196 | 6 | 3 | 1 | 0 | 0 | 2 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0005c0008 | 0/0 | 2196 | 3 | 2 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0006c0009 | 0/0 | 2196 | 3 | 3 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0007c0018 | 0/1 | 2196 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0007c0022 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0008c0011 | 0/0 | 2196 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0009c0012 | 0/0 | 2196 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0010c0013 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0011c0020 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0012c0019 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0013c0021 | 0/0 | 2196 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0014c0017 | 0/0 | 2196 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0015c0016 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0016c0024 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2595 | 192 | 44 | 42 | 74 | 13 | 18 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0001t0003 | 0/0 | 2597 | 10 | 6 | 4 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0001t0006 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0003t0001 | 0/0 | 2595 | 28 | 6 | 2 | 19 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0004t0002 | 0/0 | 2597 | 8 | 0 | 3 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0010t0001 | 0/0 | 2595 | 2 | 1 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0001c0023t0003 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0002t0002 | 0/0 | 2597 | 37 | 0 | 10 | 23 | 0 | 4 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0002t0004 | 0/0 | 2599 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0002t0007 | 0/0 | 2597 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0007t0001 | 0/0 | 2595 | 5 | 0 | 0 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0014t0002 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0002c0015t0001 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0003c0005t0001 | 0/0 | 2595 | 8 | 8 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0004c0006t0004 | 0/0 | 2599 | 5 | 2 | 1 | 0 | 0 | 2 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0004c0006t0005 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0005c0008t0001 | 0/0 | 2595 | 3 | 2 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0006c0009t0004 | 0/0 | 2599 | 3 | 3 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0007c0018t0001 | 0/1 | 2595 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0007c0022t0001 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0008c0011t0001 | 0/0 | 2595 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0009c0012t0001 | 0/0 | 2595 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0010c0013t0001 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0011c0020t0001 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0012c0019t0001 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0013c0021t0001 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0014c0017t0001 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0015c0016t0001 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
a0016c0024t0001 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | copy fasta | chr9 | 121263162 | 121337842 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0006 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0010t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0010t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0023t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0007g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0014t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0015t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0005c0008t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0005c0008t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0005c0008t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0006c0009t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0006c0009t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0007c0018t0001g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0007c0022t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0008c0011t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0009c0012t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0009c0012t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0010c0013t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0011c0020t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0012c0019t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0013c0021t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0014c0017t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0015c0016t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0016c0024t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00323 | hp1 | a0013 | c0021 | t0001 | g0108 | EUR | FIN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00558 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00621 | hp1 | a0001 | c0004 | t0002 | g0156 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00639 | hp1 | a0002 | c0015 | t0001 | g0046 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0130 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01071 | hp2 | a0004 | c0006 | t0004 | g0224 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0151 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01081 | hp1 | a0002 | c0002 | t0007 | g0076 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01109 | hp1 | a0001 | c0010 | t0001 | g0115 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01243 | hp1 | a0005 | c0008 | t0001 | g0096 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0067 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01884 | hp1 | a0004 | c0006 | t0005 | g0238 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01884 | hp2 | a0004 | c0006 | t0004 | g0185 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01891 | hp2 | a0001 | c0023 | t0003 | g0043 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01928 | hp2 | a0001 | c0004 | t0002 | g0140 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01993 | hp1 | a0001 | c0004 | t0002 | g0044 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02015 | hp2 | a0007 | c0022 | t0001 | g0182 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02027 | hp2 | a0002 | c0007 | t0001 | g0061 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0197 | EAS | CDX | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02280 | hp2 | a0003 | c0005 | t0001 | g0038 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02300 | hp2 | a0001 | c0004 | t0002 | g0045 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02451 | hp1 | a0003 | c0005 | t0001 | g0244 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02451 | hp2 | a0009 | c0012 | t0001 | g0098 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02572 | hp1 | a0002 | c0002 | t0004 | g0055 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02647 | hp2 | a0006 | c0009 | t0004 | g0037 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02717 | hp2 | a0008 | c0011 | t0001 | g0040 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02738 | hp1 | a0004 | c0006 | t0004 | g0225 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02809 | hp1 | a0009 | c0012 | t0001 | g0102 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02818 | hp2 | a0002 | c0002 | t0004 | g0054 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02886 | hp1 | a0003 | c0005 | t0001 | g0245 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02895 | hp1 | a0003 | c0005 | t0001 | g0243 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02896 | hp1 | a0006 | c0009 | t0004 | g0037 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02922 | hp1 | a0005 | c0008 | t0001 | g0095 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0227 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0228 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03017 | hp2 | a0014 | c0017 | t0001 | g0090 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03041 | hp1 | a0005 | c0008 | t0001 | g0097 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03098 | hp1 | a0008 | c0011 | t0001 | g0040 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0203 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03195 | hp1 | a0003 | c0005 | t0001 | g0248 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0262 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03225 | hp2 | a0010 | c0013 | t0001 | g0261 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03486 | hp2 | a0011 | c0020 | t0001 | g0258 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0214 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03579 | hp1 | a0004 | c0006 | t0004 | g0257 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03579 | hp2 | a0006 | c0009 | t0004 | g0241 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0239 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0057 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03710 | hp2 | a0002 | c0007 | t0001 | g0049 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03831 | hp2 | a0001 | c0004 | t0002 | g0247 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG04199 | hp1 | a0004 | c0006 | t0004 | g0240 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18522 | hp1 | a0001 | c0010 | t0001 | g0114 | AFR | YRI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | CHB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | CHB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0213 | AFR | YRI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18906 | hp2 | a0016 | c0024 | t0001 | g0101 | AFR | YRI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18939 | hp2 | a0002 | c0014 | t0002 | g0048 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18944 | hp1 | a0002 | c0007 | t0001 | g0056 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18949 | hp2 | a0001 | c0004 | t0002 | g0123 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18952 | hp2 | a0001 | c0004 | t0002 | g0175 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18954 | hp2 | a0002 | c0007 | t0001 | g0072 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18957 | hp2 | a0001 | c0004 | t0002 | g0172 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0100 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18999 | hp1 | a0002 | c0007 | t0001 | g0065 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19004 | hp2 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19043 | hp1 | a0003 | c0005 | t0001 | g0246 | AFR | LWK | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19066 | hp1 | a0015 | c0016 | t0001 | g0260 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19070 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ASW | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA20129 | hp2 | a0003 | c0005 | t0001 | g0038 | AFR | ASW | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02559 | hp2 | a0012 | c0019 | t0001 | g0232 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03471 | hp2 | a0003 | c0005 | t0001 | g0242 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | USA | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
homoSapiens_chm13v2 | hp1 | a0007 | c0018 | t0001 | g0091 | REF | REF | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0047 | REF | REF | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121302000
|
A | G | 2 | a0003a0006 | 11 | HG02280.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
missense_variant | MODERATE | c.29A>G | p.Lys10Arg | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 189/2595 | 29/2196 | 10/731 | chr9 | 121302000 | ||
chr9:121302046
|
C | G | 2 | a0009a0016 | 3 | HG02451.hp2 HG02809.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.75C>G | p.Phe25Leu | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 235/2595 | 75/2196 | 25/731 | chr9 | 121302046 | ||
chr9:121302098
|
G | T | 1 | a0008 | 2 | HG02717.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.127G>T | p.Ala43Ser | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 287/2595 | 127/2196 | 43/731 | chr9 | 121302098 | ||
chr9:121302104
|
G | A | 1 | a0010 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.133G>A | p.Val45Ile | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 293/2595 | 133/2196 | 45/731 | chr9 | 121302104 | ||
chr9:121302946
|
G | A | 2 | a0002a0015 | 48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
missense_variant | MODERATE | c.232G>A | p.Ala78Thr | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/18 | 392/2595 | 232/2196 | 78/731 | chr9 | 121302946 | ||
chr9:121312363
|
A | G | 1 | a0005 | 3 | HG01243.hp1 HG02922.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.538A>G | p.Asn180Asp | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/18 | 698/2595 | 538/2196 | 180/731 | chr9 | 121312363 | ||
chr9:121312456
|
G | C | 1 | a0014 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.631G>C | p.Glu211Gln | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/18 | 791/2595 | 631/2196 | 211/731 | chr9 | 121312456 | ||
chr9:121314000
|
C | T | 1 | a0015 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.730C>T | p.Arg244Cys | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/18 | 890/2595 | 730/2196 | 244/731 | chr9 | 121314000 | ||
chr9:121326630
|
C | G | 1 | a0004 | 6 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
missense_variant | MODERATE | c.1535C>G | p.Thr512Ser | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/18 | 1695/2595 | 1535/2196 | 512/731 | chr9 | 121326630 | ||
chr9:121327357
|
A | G | 1 | a0013 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.1637A>G | p.Lys546Arg | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/18 | 1797/2595 | 1637/2196 | 546/731 | chr9 | 121327357 | ||
chr9:121327414
|
C | T | 4 | a0003a0004a0011others(1): Show | 16 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
missense_variant | MODERATE | c.1694C>T | p.Thr565Met | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/18 | 1854/2595 | 1694/2196 | 565/731 | chr9 | 121327414 | ||
chr9:121328978
|
G | T | 1 | a0012 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1850G>T | p.Arg617Leu | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 15/18 | 2010/2595 | 1850/2196 | 617/731 | chr9 | 121328978 | ||
chr9:121329281
|
C | T | 1 | a0007 | 2 | HG02015.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.1931C>T | p.Thr644Met | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/18 | 2091/2595 | 1931/2196 | 644/731 | chr9 | 121329281 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121302157
|
C | T | 1 | a0008c0011 | 2 | HG02717.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.186C>T | p.His62His | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 346/2595 | 186/2196 | 62/731 | chr9 | 121302157 | ||
chr9:121302957
|
C | T | 1 | a0001c0023 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.243C>T | p.Thr81Thr | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/18 | 403/2595 | 243/2196 | 81/731 | chr9 | 121302957 | ||
chr9:121321315
|
A | G | 1 | a0001c0010 | 2 | HG01109.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.1239A>G | p.Thr413Thr | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/18 | 1399/2595 | 1239/2196 | 413/731 | chr9 | 121321315 | ||
chr9:121321336
|
C | T | 2 | a0001c0003a0002c0015 | 29 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
synonymous_variant | LOW | c.1260C>T | p.Gly420Gly | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/18 | 1420/2595 | 1260/2196 | 420/731 | chr9 | 121321336 | ||
chr9:121326538
|
C | T | 1 | a0002c0014 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.1443C>T | p.Pro481Pro | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/18 | 1603/2595 | 1443/2196 | 481/731 | chr9 | 121326538 | ||
chr9:121326580
|
C | T | 1 | a0007c0022 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1485C>T | p.Ile495Ile | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/18 | 1645/2595 | 1485/2196 | 495/731 | chr9 | 121326580 | ||
chr9:121332522
|
T | C | 8 | a0001c0004a0002c0002a0002c0014others(5): Show | 64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
synonymous_variant | LOW | c.2115T>C | p.Phe705Phe | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 2275/2595 | 2115/2196 | 705/731 | chr9 | 121332522 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121268202
|
C | G | 1 | a0002c0002t0007 | 1 | HG01081.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-120C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/18 | chr9 | 121268202 | ||||||
chr9:121281478
|
C | T | 1 | a0001c0001t0006 | 1 | HG00558.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/18 | 20494 | chr9 | 121281478 | |||||
chr9:121281480
|
T | C | 1 | a0004c0006t0005 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/18 | 20492 | chr9 | 121281480 | |||||
chr9:121332699
|
A | AGT | 2 | a0001c0001t0003a0001c0023t0003 | 11 | HG01255.hp1 HG01891.hp2 HG01934.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*115_*116dupGT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 117 | INFO_REALIGN_3_PRIME | chr9 | 121332699 | ||||
chr9:121332699
|
A | AGTGT | 3 | a0002c0002t0004a0004c0006t0004a0006c0009t0004 | 10 | HG01071.hp2 HG01884.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*113_*116dupGTGT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 117 | INFO_REALIGN_3_PRIME | chr9 | 121332699 | ||||
chr9:121332719
|
T | TG | 4 | a0001c0004t0002a0002c0002t0002a0002c0002t0007others(1): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*116_*117insG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 117 | chr9 | 121332719 | |||||
chr9:121332723
|
T | TG | 4 | a0001c0004t0002a0002c0002t0002a0002c0002t0007others(1): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*120_*121insG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 121 | chr9 | 121332723 | |||||
chr9:121332725
|
C | T | 4 | a0001c0004t0002a0002c0002t0002a0002c0002t0007others(1): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*122C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 122 | chr9 | 121332725 | |||||
chr9:121332727
|
T | C | 4 | a0001c0004t0002a0002c0002t0002a0002c0002t0007others(1): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*124T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 124 | chr9 | 121332727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121268281
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-103+62T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121268281 | ||||||
chr9:121268283
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | NA18953.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-103+64C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121268283 | ||||||
chr9:121268305
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0263a0001c0003t0001g0262 | 4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+86A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121268305 | ||||||
chr9:121268803
|
G | T | 1 | a0010c0013t0001g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-103+584G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121268803 | ||||||
chr9:121269474
|
G | A | 1 | a0001c0023t0003g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-103+1255G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269474 | ||||||
chr9:121269615
|
C | T | 1 | a0015c0016t0001g0260 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-103+1396C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269615 | ||||||
chr9:121269769
|
T | C | 2 | a0001c0004t0002g0044a0001c0004t0002g0045 | 2 | HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-103+1550T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269769 | ||||||
chr9:121269809
|
A | C | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103+1590A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269809 | ||||||
chr9:121269824
|
A | T | 4 | a0001c0001t0001g0259a0004c0006t0004g0257a0010c0013t0001g0261others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+1605A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269824 | ||||||
chr9:121269857
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-103+1638C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269857 | ||||||
chr9:121270102
|
G | A | 1 | a0002c0015t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-103+1883G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121270102 | ||||||
chr9:121270589
|
C | T | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-103+2370C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121270589 | ||||||
chr9:121270710
|
G | T | 1 | a0002c0002t0002g0255 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-103+2491G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121270710 | ||||||
chr9:121270766
|
C | A | 99 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(96): Show | 116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-103+2547C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121270766 | ||||||
chr9:121270902
|
GTGTGTAT others(3): Show |
G | 1 | a0001c0001t0001g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-103+2686_-103+269 others(14): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121270902 | |||||
chr9:121272098
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0253a0001c0001t0001g0254 | 4 | HG02129.hp1 NA18943.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+3879C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272098 | ||||||
chr9:121272111
|
G | C | 1 | a0002c0014t0002g0048 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-103+3892G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272111 | ||||||
chr9:121272117
|
G | C | 1 | a0004c0006t0004g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-103+3898G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272117 | ||||||
chr9:121272234
|
C | T | 4 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(1): Show | 4 | NA18939.hp1 NA18960.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+4015C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272234 | ||||||
chr9:121272431
|
ATAATGTC others(4): Show |
A | 1 | a0001c0001t0001g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-103+4214_-103+422 others(15): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121272431 | |||||
chr9:121272531
|
G | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(77): Show | 97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103+4312G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272531 | ||||||
chr9:121272581
|
G | A | 1 | a0001c0023t0003g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-103+4362G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272581 | ||||||
chr9:121272700
|
C | T | 1 | a0003c0005t0001g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-103+4481C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272700 | ||||||
chr9:121272702
|
A | G | 1 | a0001c0004t0002g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-103+4483A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272702 | ||||||
chr9:121272783
|
C | T | 10 | a0001c0023t0003g0043a0003c0005t0001g0038a0003c0005t0001g0242others(7): Show | 12 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+4564C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272783 | ||||||
chr9:121272866
|
T | A | 1 | a0007c0022t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-103+4647T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272866 | ||||||
chr9:121272950
|
A | G | 10 | a0001c0023t0003g0043a0003c0005t0001g0038a0003c0005t0001g0242others(7): Show | 12 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+4731A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272950 | ||||||
chr9:121273021
|
G | C | 1 | a0001c0001t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-103+4802G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273021 | ||||||
chr9:121273038
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-103+4819A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273038 | ||||||
chr9:121273102
|
T | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-103+4883T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273102 | ||||||
chr9:121273129
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-103+4910G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273129 | ||||||
chr9:121273267
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 117 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-103+5048A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273267 | ||||||
chr9:121273449
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-103+5230C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273449 | ||||||
chr9:121273818
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 117 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-103+5599A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273818 | ||||||
chr9:121273863
|
G | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0180 | 4 | NA18977.hp1 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+5644G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273863 | ||||||
chr9:121273925
|
G | A | 39 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(36): Show | 48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-103+5706G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273925 | ||||||
chr9:121273967
|
A | T | 39 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(36): Show | 48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-103+5748A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273967 | ||||||
chr9:121274253
|
CT | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(2): Show | 8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-103+6043delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121274253 | |||||
chr9:121274342
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-103+6123C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274342 | ||||||
chr9:121274509
|
T | TA | 15 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(12): Show | 20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-103+6300dupA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121274509 | |||||
chr9:121274519
|
A | T | 1 | a0004c0006t0004g0240 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-103+6300A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274519 | ||||||
chr9:121274543
|
G | A | 1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-103+6324G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274543 | ||||||
chr9:121274745
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-103+6526G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274745 | ||||||
chr9:121274992
|
C | G | 1 | a0011c0020t0001g0258 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-102-6478C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274992 | ||||||
chr9:121275008
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-102-6462C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275008 | ||||||
chr9:121275022
|
C | T | 1 | a0001c0003t0001g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-102-6448C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275022 | ||||||
chr9:121275073
|
G | C | 1 | a0002c0002t0002g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-102-6397G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275073 | ||||||
chr9:121275189
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-102-6281A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275189 | ||||||
chr9:121275329
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-6141C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275329 | ||||||
chr9:121275493
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(12): Show | 20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-102-5977G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275493 | ||||||
chr9:121275613
|
C | T | 1 | a0004c0006t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-102-5857C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275613 | ||||||
chr9:121275739
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-102-5731A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275739 | ||||||
chr9:121275941
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-102-5529A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275941 | ||||||
chr9:121275954
|
A | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0235a0001c0001t0001g0236 | 4 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-5516A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275954 | ||||||
chr9:121275977
|
A | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0184a0001c0001t0001g0259others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-102-5493A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275977 | ||||||
chr9:121276172
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 5 | HG01070.hp2 HG01358.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-5298G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276172 | ||||||
chr9:121276189
|
C | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-5281C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276189 | ||||||
chr9:121276216
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-102-5254C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276216 | ||||||
chr9:121276313
|
C | T | 7 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0176others(4): Show | 7 | HG00621.hp2 HG02071.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102-5157C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276313 | ||||||
chr9:121276366
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-102-5104T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276366 | ||||||
chr9:121276534
|
C | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-102-4936C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276534 | ||||||
chr9:121276848
|
G | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-4622G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276848 | ||||||
chr9:121277025
|
T | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0259a0004c0006t0004g0257 | 3 | HG02109.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-102-4445T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277025 | ||||||
chr9:121277448
|
A | T | 1 | a0003c0005t0001g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-102-4022A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277448 | ||||||
chr9:121277456
|
A | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-102-4014A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277456 | ||||||
chr9:121277593
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-3877C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277593 | ||||||
chr9:121277618
|
C | T | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-102-3852C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277618 | ||||||
chr9:121277653
|
T | TAAAATAC others(308): Show |
1 | a0002c0015t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(319): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(310): Show |
1 | a0002c0002t0007g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(321): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(312): Show |
2 | a0002c0002t0002g0013a0002c0002t0002g0075 | 3 | HG00438.hp2 HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(323): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(313): Show |
2 | a0002c0002t0002g0074a0002c0002t0002g0255 | 2 | NA18979.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(324): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(314): Show |
1 | a0002c0002t0002g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(325): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(327): Show |
7 | a0002c0002t0002g0007a0002c0002t0002g0012a0002c0002t0002g0068others(4): Show | 10 | HG02273.hp1 NA18612.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(338): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(328): Show |
10 | a0002c0002t0002g0002a0002c0002t0002g0011a0002c0002t0002g0062others(7): Show | 14 | HG01123.hp2 HG01168.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(339): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(329): Show |
5 | a0002c0002t0002g0010a0002c0002t0002g0058a0002c0002t0002g0059others(2): Show | 6 | HG00597.hp1 HG01106.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(340): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(330): Show |
4 | a0002c0002t0002g0050a0002c0002t0002g0057a0002c0002t0004g0055others(1): Show | 4 | HG02572.hp1 HG03654.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(341): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(331): Show |
1 | a0002c0002t0004g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(342): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(332): Show |
1 | a0002c0002t0002g0053 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(343): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(334): Show |
1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(345): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(337): Show |
2 | a0002c0002t0002g0051a0002c0002t0002g0052 | 2 | NA18964.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(348): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277653
|
T | TAAAATAC others(326): Show |
1 | a0002c0002t0002g0077 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(337): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | |||||
chr9:121277866
|
C | T | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(50): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-102-3604C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277866 | ||||||
chr9:121277918
|
TAACA | T | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(50): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-102-3542_-102-353 others(8): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277918 | |||||
chr9:121278030
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-102-3440G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278030 | ||||||
chr9:121278051
|
CT | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(3): Show | 6 | HG00735.hp1 HG01070.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-102-3405delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121278051 | |||||
chr9:121278307
|
A | G | 2 | a0001c0001t0001g0171a0001c0003t0001g0170 | 2 | NA18967.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-102-3163A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278307 | ||||||
chr9:121278343
|
C | T | 1 | a0001c0003t0001g0262 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-102-3127C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278343 | ||||||
chr9:121278400
|
C | T | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(50): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-102-3070C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278400 | ||||||
chr9:121278450
|
A | C | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-102-3020A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278450 | ||||||
chr9:121278511
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0120a0001c0001t0001g0121 | 4 | HG00280.hp2 HG01099.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-2959C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278511 | ||||||
chr9:121278594
|
T | C | 1 | a0004c0006t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-102-2876T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278594 | ||||||
chr9:121278678
|
AC | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(2): Show | 8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-102-2789delC | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121278678 | |||||
chr9:121278719
|
G | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-2751G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278719 | ||||||
chr9:121278907
|
C | A | 1 | a0001c0001t0001g0264 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-102-2563C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278907 | ||||||
chr9:121278948
|
G | A | 1 | a0002c0002t0002g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-102-2522G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278948 | ||||||
chr9:121278968
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(12): Show | 20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-102-2502C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278968 | ||||||
chr9:121279061
|
C | T | 1 | a0002c0015t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-102-2409C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279061 | ||||||
chr9:121279072
|
G | T | 1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-102-2398G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279072 | ||||||
chr9:121279393
|
T | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-102-2077T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279393 | ||||||
chr9:121279539
|
C | T | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(257): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-102-1931C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279539 | ||||||
chr9:121279623
|
G | A | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-102-1847G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279623 | ||||||
chr9:121279766
|
G | A | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-102-1704G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279766 | ||||||
chr9:121279774
|
C | T | 2 | a0001c0001t0003g0233a0012c0019t0001g0232 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-102-1696C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279774 | ||||||
chr9:121279810
|
G | A | 2 | a0010c0013t0001g0261a0011c0020t0001g0258 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-102-1660G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279810 | ||||||
chr9:121279915
|
G | A | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-102-1555G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279915 | ||||||
chr9:121279946
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0080a0001c0001t0001g0083others(10): Show | 14 | HG00099.hp2 HG00738.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.-102-1524T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279946 | ||||||
chr9:121280322
|
G | A | 1 | a0004c0006t0004g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-102-1148G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280322 | ||||||
chr9:121280457
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(11): Show | 19 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-102-1013C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280457 | ||||||
chr9:121280522
|
T | C | 6 | a0001c0001t0001g0184a0001c0001t0001g0259a0004c0006t0004g0185others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102-948T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280522 | ||||||
chr9:121280540
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-102-930C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280540 | ||||||
chr9:121280666
|
C | T | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(259): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-102-804C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280666 | ||||||
chr9:121280912
|
TA | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(11): Show | 19 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-102-557delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280912 | ||||||
chr9:121281150
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-102-320C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121281150 | ||||||
chr9:121281173
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-102-297G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121281173 | ||||||
chr9:121281189
|
G | A | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(50): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-102-281G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121281189 | ||||||
chr9:121281282
|
G | T | 2 | a0001c0001t0003g0116a0001c0001t0003g0117 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-102-188G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121281282 | ||||||
chr9:121281582
|
CA | C | 36 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(33): Show | 45 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-10+21delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121281582 | ||||||
chr9:121281589
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-10+27C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121281589 | ||||||
chr9:121282054
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-10+492C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282054 | ||||||
chr9:121282131
|
G | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0229 | 2 | HG02486.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-10+569G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282131 | ||||||
chr9:121282209
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-10+647T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282209 | ||||||
chr9:121282340
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(2): Show | 8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+778G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282340 | ||||||
chr9:121282373
|
T | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0263a0006c0009t0004g0037 | 5 | HG02647.hp2 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+811T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282373 | ||||||
chr9:121282441
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-10+879G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282441 | ||||||
chr9:121282708
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-10+1146C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282708 | ||||||
chr9:121282717
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+1155C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282717 | ||||||
chr9:121282760
|
A | G | 1 | a0002c0002t0002g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-10+1198A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282760 | ||||||
chr9:121282868
|
C | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-10+1306C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282868 | ||||||
chr9:121282873
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10+1311A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282873 | ||||||
chr9:121282906
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0120a0001c0001t0001g0121 | 4 | HG00280.hp2 HG01099.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+1344C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282906 | ||||||
chr9:121282915
|
A | G | 1 | a0010c0013t0001g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10+1353A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282915 | ||||||
chr9:121282919
|
C | T | 1 | a0001c0003t0001g0262 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10+1357C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282919 | ||||||
chr9:121283138
|
TTCTCTTT others(71): Show |
T | 1 | a0002c0002t0002g0060 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-10+1611_-10+1688d others(80): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283138 | |||||
chr9:121283180
|
TAGTTAGG others(14): Show |
T | 5 | a0001c0001t0001g0184a0001c0001t0001g0259a0004c0006t0004g0257others(2): Show | 5 | HG02109.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1630_-10+1650d others(23): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283180 | |||||
chr9:121283250
|
G | A | 1 | a0001c0003t0001g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-10+1688G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283250 | ||||||
chr9:121283301
|
CT | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(81): Show | 101 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.-10+1754delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283301 | |||||
chr9:121283393
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-10+1831G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283393 | ||||||
chr9:121283458
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 4 | HG01123.hp1 HG01358.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+1896C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283458 | ||||||
chr9:121283498
|
A | G | 1 | a0001c0003t0001g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10+1936A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283498 | ||||||
chr9:121283644
|
C | A | 1 | a0004c0006t0004g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10+2082C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283644 | ||||||
chr9:121283671
|
G | GTTCA | 33 | a0001c0001t0001g0041a0001c0001t0001g0263a0001c0001t0003g0233others(30): Show | 42 | HG00438.hp2 HG00597.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.-10+2143_-10+2146d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | |||||
chr9:121283671
|
G | GTTCATTC others(1): Show |
14 | a0001c0001t0001g0184a0001c0001t0001g0259a0002c0002t0002g0011others(11): Show | 15 | HG01106.hp1 HG01123.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10+2139_-10+2146d others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | |||||
chr9:121283671
|
G | GTTCATTC others(5): Show |
1 | a0002c0002t0007g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-10+2135_-10+2146d others(14): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | |||||
chr9:121283671
|
GTTCA | G | 105 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(102): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.-10+2143_-10+2146d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | |||||
chr9:121283671
|
GTTCATTC others(1): Show |
G | 2 | a0001c0001t0001g0094a0008c0011t0001g0040 | 3 | HG02717.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-10+2139_-10+2146d others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | |||||
chr9:121283671
|
GTTCATTC others(9): Show |
G | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+2131_-10+2146d others(18): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | |||||
chr9:121283680
|
T | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(11): Show | 19 | HG01261.hp1 HG02055.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+2118T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283680 | ||||||
chr9:121283684
|
T | C | 1 | a0001c0023t0003g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-10+2122T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283684 | ||||||
chr9:121283696
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+2134T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283696 | ||||||
chr9:121283800
|
G | A | 1 | a0002c0002t0004g0055 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-10+2238G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283800 | ||||||
chr9:121284033
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-10+2471G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284033 | ||||||
chr9:121284355
|
G | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG00140.hp2 HG01261.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-10+2793G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284355 | ||||||
chr9:121284413
|
G | T | 54 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(51): Show | 61 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10+2851G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284413 | ||||||
chr9:121284444
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+2882C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284444 | ||||||
chr9:121284499
|
A | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(12): Show | 20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+2937A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284499 | ||||||
chr9:121284552
|
CT | C | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(259): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-10+2992delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121284552 | |||||
chr9:121284787
|
G | A | 5 | a0001c0001t0001g0184a0001c0001t0001g0259a0004c0006t0004g0257others(2): Show | 5 | HG02109.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+3225G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284787 | ||||||
chr9:121284818
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-10+3256A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284818 | ||||||
chr9:121284898
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-10+3336C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284898 | ||||||
chr9:121284957
|
G | A | 3 | a0005c0008t0001g0095a0005c0008t0001g0096a0005c0008t0001g0097 | 3 | HG01243.hp1 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-10+3395G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284957 | ||||||
chr9:121284959
|
T | C | 54 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(51): Show | 61 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10+3397T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284959 | ||||||
chr9:121284968
|
A | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-10+3406A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284968 | ||||||
chr9:121284980
|
A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(11): Show | 19 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10+3418A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284980 | ||||||
chr9:121285219
|
C | T | 1 | a0010c0013t0001g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10+3657C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285219 | ||||||
chr9:121285496
|
A | G | 39 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(36): Show | 48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10+3934A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285496 | ||||||
chr9:121285555
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0120a0001c0001t0001g0121 | 4 | HG00280.hp2 HG01099.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+3993T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285555 | ||||||
chr9:121285558
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-10+3996T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285558 | ||||||
chr9:121285706
|
A | G | 1 | a0003c0005t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+4144A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285706 | ||||||
chr9:121285797
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10+4235T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285797 | ||||||
chr9:121285900
|
C | A | 1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-10+4338C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285900 | ||||||
chr9:121286020
|
G | A | 51 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(48): Show | 58 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-10+4458G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286020 | ||||||
chr9:121286030
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-10+4468C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286030 | ||||||
chr9:121286183
|
T | C | 45 | a0001c0001t0001g0184a0001c0001t0001g0259a0002c0002t0002g0002others(42): Show | 54 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10+4621T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286183 | ||||||
chr9:121286343
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 6 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+4781A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286343 | ||||||
chr9:121286351
|
C | G | 1 | a0001c0001t0001g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-10+4789C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286351 | ||||||
chr9:121286361
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-10+4799G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286361 | ||||||
chr9:121286378
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-10+4816G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286378 | ||||||
chr9:121286449
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-10+4887C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286449 | ||||||
chr9:121286526
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0229 | 2 | HG01175.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-10+4964C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286526 | ||||||
chr9:121287005
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-10+5443C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287005 | ||||||
chr9:121287065
|
G | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(2): Show | 8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+5503G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287065 | ||||||
chr9:121287226
|
G | A | 1 | a0009c0012t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-10+5664G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287226 | ||||||
chr9:121287358
|
G | T | 1 | a0003c0005t0001g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+5796G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287358 | ||||||
chr9:121287383
|
G | A | 1 | a0001c0003t0001g0132 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-10+5821G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287383 | ||||||
chr9:121287435
|
G | A | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(50): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-10+5873G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287435 | ||||||
chr9:121287439
|
C | T | 39 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(36): Show | 48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10+5877C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287439 | ||||||
chr9:121287459
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0122 | 4 | HG02809.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+5897T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287459 | ||||||
chr9:121287630
|
G | A | 1 | a0010c0013t0001g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10+6068G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287630 | ||||||
chr9:121287678
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+6116T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287678 | ||||||
chr9:121287682
|
C | CT | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-10+6129dupT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121287682 | |||||
chr9:121287692
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0162a0001c0001t0001g0178 | 3 | NA18959.hp1 NA18969.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-10+6130C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287692 | ||||||
chr9:121287693
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0162 | 2 | NA18959.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-10+6131T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287693 | ||||||
chr9:121287702
|
T | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(12): Show | 20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+6140T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287702 | ||||||
chr9:121287703
|
A | T | 1 | a0002c0002t0002g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-10+6141A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287703 | ||||||
chr9:121287901
|
C | T | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+6339C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287901 | ||||||
chr9:121287981
|
C | T | 45 | a0001c0001t0001g0184a0001c0001t0001g0259a0002c0002t0002g0002others(42): Show | 54 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10+6419C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287981 | ||||||
chr9:121288051
|
C | T | 1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-10+6489C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288051 | ||||||
chr9:121288389
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 4 | HG01123.hp1 HG01358.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+6827C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288389 | ||||||
chr9:121288461
|
G | C | 1 | a0007c0022t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-10+6899G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288461 | ||||||
chr9:121288530
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0112 | 4 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+6968A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288530 | ||||||
chr9:121288560
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0124others(8): Show | 15 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+6998G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288560 | ||||||
chr9:121288813
|
A | ATAG | 4 | a0001c0001t0003g0017a0001c0001t0003g0109a0001c0001t0003g0116others(1): Show | 5 | HG02145.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+7254_-10+7256d others(5): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121288813 | |||||
chr9:121288820
|
A | G | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+7258A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288820 | ||||||
chr9:121289004
|
A | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(12): Show | 20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+7442A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289004 | ||||||
chr9:121289122
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-10+7560A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289122 | ||||||
chr9:121289161
|
T | G | 1 | a0001c0001t0001g0133 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-10+7599T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289161 | ||||||
chr9:121289240
|
G | A | 1 | a0001c0003t0001g0100 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-10+7678G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289240 | ||||||
chr9:121289313
|
G | A | 1 | a0004c0006t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+7751G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289313 | ||||||
chr9:121289334
|
G | A | 1 | a0004c0006t0004g0224 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-10+7772G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289334 | ||||||
chr9:121289545
|
G | T | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+7983G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289545 | ||||||
chr9:121289557
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-10+7995C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289557 | ||||||
chr9:121289622
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-10+8060C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289622 | ||||||
chr9:121289623
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10+8061C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289623 | ||||||
chr9:121289653
|
G | A | 39 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(36): Show | 48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10+8091G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289653 | ||||||
chr9:121289794
|
G | T | 40 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(37): Show | 50 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-10+8232G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289794 | ||||||
chr9:121289984
|
A | G | 2 | a0002c0002t0002g0057a0002c0002t0002g0062 | 2 | HG03490.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-10+8422A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289984 | ||||||
chr9:121289999
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-10+8437A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289999 | ||||||
chr9:121290120
|
G | C | 3 | a0001c0001t0001g0041a0001c0001t0001g0263a0001c0003t0001g0262 | 4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+8558G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290120 | ||||||
chr9:121290262
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-10+8700C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290262 | ||||||
chr9:121290266
|
A | G | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+8704A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290266 | ||||||
chr9:121290367
|
T | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0263a0001c0003t0001g0262 | 4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+8805T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290367 | ||||||
chr9:121290518
|
T | C | 1 | a0004c0006t0004g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10+8956T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290518 | ||||||
chr9:121290572
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-10+9010T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290572 | ||||||
chr9:121290590
|
C | T | 1 | a0007c0018t0001g0091 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-10+9028C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290590 | ||||||
chr9:121290610
|
G | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+9048G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290610 | ||||||
chr9:121290622
|
G | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0253a0001c0001t0001g0254 | 4 | HG02129.hp1 NA18943.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+9060G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290622 | ||||||
chr9:121290706
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(12): Show | 20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+9144G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290706 | ||||||
chr9:121290783
|
T | G | 1 | a0001c0001t0001g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10+9221T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290783 | ||||||
chr9:121290875
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-10+9313C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290875 | ||||||
chr9:121291367
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-10+9805C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291367 | ||||||
chr9:121291401
|
T | C | 3 | a0005c0008t0001g0095a0005c0008t0001g0096a0005c0008t0001g0097 | 3 | HG01243.hp1 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-10+9839T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291401 | ||||||
chr9:121291416
|
CT | C | 14 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0001g0263others(11): Show | 15 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10+9874delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121291416 | |||||
chr9:121291416
|
CTT | C | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(175): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.-10+9873_-10+9874d others(4): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121291416 | |||||
chr9:121291416
|
CTTT | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0127a0001c0001t0001g0183others(8): Show | 14 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+9872_-10+9874d others(5): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121291416 | |||||
chr9:121291482
|
G | A | 1 | a0002c0002t0002g0051 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-10+9920G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291482 | ||||||
chr9:121291482
|
G | T | 1 | a0004c0006t0004g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+9920G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291482 | ||||||
chr9:121291494
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0259a0004c0006t0004g0257 | 3 | HG02109.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-10+9932C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291494 | ||||||
chr9:121291580
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-10+10018G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291580 | ||||||
chr9:121291608
|
T | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-10+10046T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291608 | ||||||
chr9:121292564
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-9-9399G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121292564 | ||||||
chr9:121292809
|
T | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0263a0001c0001t0003g0233others(2): Show | 6 | HG02486.hp2 HG02559.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-9154T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121292809 | ||||||
chr9:121292958
|
C | T | 38 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(35): Show | 47 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9-9005C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121292958 | ||||||
chr9:121293026
|
A | G | 1 | a0013c0021t0001g0108 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-9-8937A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293026 | ||||||
chr9:121293039
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9-8924G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293039 | ||||||
chr9:121293040
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9-8923A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293040 | ||||||
chr9:121293113
|
G | A | 4 | a0001c0001t0001g0118a0009c0012t0001g0098a0009c0012t0001g0102others(1): Show | 4 | HG02451.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-8850G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293113 | ||||||
chr9:121293133
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0263a0001c0003t0001g0262 | 4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-8830C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293133 | ||||||
chr9:121293146
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9-8817G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293146 | ||||||
chr9:121293292
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0136 | 3 | HG01106.hp2 HG01192.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-9-8671G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293292 | ||||||
chr9:121293409
|
AT | A | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-9-8541delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121293409 | |||||
chr9:121293577
|
C | A | 1 | a0001c0001t0001g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-9-8386C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293577 | ||||||
chr9:121293608
|
A | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-8355A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293608 | ||||||
chr9:121293654
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0078a0001c0001t0001g0080others(14): Show | 18 | HG00099.hp2 HG00323.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-8309C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293654 | ||||||
chr9:121293697
|
CA | C | 45 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0219others(42): Show | 54 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-9-8248delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121293697 | |||||
chr9:121293697
|
CAA | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-9-8249_-9-8248del others(2): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121293697 | |||||
chr9:121293743
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-8220T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293743 | ||||||
chr9:121293765
|
G | A | 1 | a0004c0006t0004g0225 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9-8198G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293765 | ||||||
chr9:121293769
|
T | G | 1 | a0001c0003t0001g0262 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-9-8194T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293769 | ||||||
chr9:121293958
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0263a0001c0003t0001g0262 | 4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-8005A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293958 | ||||||
chr9:121293968
|
AG | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-7994delG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293968 | ||||||
chr9:121294150
|
G | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-7813G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294150 | ||||||
chr9:121294236
|
C | T | 10 | a0001c0023t0003g0043a0003c0005t0001g0038a0003c0005t0001g0242others(7): Show | 12 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-7727C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294236 | ||||||
chr9:121294254
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0122others(3): Show | 7 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-7709T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294254 | ||||||
chr9:121294348
|
C | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-9-7615C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294348 | ||||||
chr9:121294352
|
C | T | 1 | a0001c0004t0002g0156 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-9-7611C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294352 | ||||||
chr9:121294451
|
T | C | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-7512T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294451 | ||||||
chr9:121294903
|
AG | A | 3 | a0009c0012t0001g0098a0009c0012t0001g0102a0016c0024t0001g0101 | 3 | HG02451.hp2 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-9-7059delG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294903 | ||||||
chr9:121295254
|
G | A | 1 | a0001c0004t0002g0172 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-9-6709G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295254 | ||||||
chr9:121295301
|
G | A | 1 | a0002c0015t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-6662G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295301 | ||||||
chr9:121295404
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-6559C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295404 | ||||||
chr9:121295559
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0128 | 2 | HG01358.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-9-6404G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295559 | ||||||
chr9:121295561
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-9-6402G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295561 | ||||||
chr9:121295709
|
C | T | 1 | a0001c0003t0001g0218 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-9-6254C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295709 | ||||||
chr9:121295807
|
G | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0131others(9): Show | 14 | HG00621.hp2 HG02071.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-6156G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295807 | ||||||
chr9:121295935
|
T | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 117 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-9-6028T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295935 | ||||||
chr9:121295989
|
C | A | 1 | a0002c0015t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-5974C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295989 | ||||||
chr9:121296081
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-5882C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296081 | ||||||
chr9:121296098
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-9-5865C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296098 | ||||||
chr9:121296521
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-9-5442T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296521 | ||||||
chr9:121296665
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-5298C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296665 | ||||||
chr9:121296769
|
G | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-9-5194G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296769 | ||||||
chr9:121296807
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-9-5156G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296807 | ||||||
chr9:121296899
|
T | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 117 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-9-5064T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296899 | ||||||
chr9:121297372
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9-4591C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297372 | ||||||
chr9:121297651
|
T | G | 1 | a0011c0020t0001g0258 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-9-4312T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297651 | ||||||
chr9:121297697
|
G | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-9-4266G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297697 | ||||||
chr9:121297774
|
G | A | 36 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(33): Show | 45 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-9-4189G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297774 | ||||||
chr9:121297901
|
A | C | 10 | a0001c0023t0003g0043a0003c0005t0001g0038a0003c0005t0001g0242others(7): Show | 12 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-4062A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297901 | ||||||
chr9:121297952
|
T | C | 6 | a0001c0001t0001g0184a0001c0001t0001g0259a0004c0006t0004g0185others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-4011T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297952 | ||||||
chr9:121298026
|
C | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(75): Show | 95 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-9-3937C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298026 | ||||||
chr9:121298144
|
G | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-9-3819G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298144 | ||||||
chr9:121298305
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(2): Show | 8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-3658C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298305 | ||||||
chr9:121298472
|
C | T | 1 | a0001c0023t0003g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9-3491C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298472 | ||||||
chr9:121298601
|
T | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-9-3362T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298601 | ||||||
chr9:121298681
|
G | T | 1 | a0015c0016t0001g0260 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-9-3282G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298681 | ||||||
chr9:121298711
|
C | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-3252C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298711 | ||||||
chr9:121298986
|
A | G | 40 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(37): Show | 50 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-9-2977A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298986 | ||||||
chr9:121299012
|
G | C | 1 | a0001c0003t0001g0132 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-9-2951G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299012 | ||||||
chr9:121299119
|
T | C | 1 | a0001c0003t0001g0009 | 3 | HG00558.hp2 HG02015.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-9-2844T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299119 | ||||||
chr9:121299522
|
TAGGTGCG others(3): Show |
T | 1 | a0004c0006t0004g0225 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9-2437_-9-2428del others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121299522 | |||||
chr9:121299557
|
C | T | 45 | a0001c0001t0001g0184a0001c0001t0001g0259a0002c0002t0002g0002others(42): Show | 55 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.-9-2406C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299557 | ||||||
chr9:121299582
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-9-2381C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299582 | ||||||
chr9:121299590
|
C | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-9-2373C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299590 | ||||||
chr9:121299614
|
A | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0168 | 2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-9-2349A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299614 | ||||||
chr9:121299622
|
C | A | 2 | a0001c0010t0001g0114a0001c0010t0001g0115 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-9-2341C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299622 | ||||||
chr9:121299624
|
C | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-9-2339C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299624 | ||||||
chr9:121299666
|
G | A | 1 | a0004c0006t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-2297G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299666 | ||||||
chr9:121299685
|
G | A | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(50): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-9-2278G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299685 | ||||||
chr9:121299752
|
G | A | 1 | a0001c0003t0001g0220 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-9-2211G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299752 | ||||||
chr9:121299849
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-9-2114C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299849 | ||||||
chr9:121300482
|
C | T | 1 | a0001c0010t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-9-1481C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121300482 | ||||||
chr9:121300737
|
C | T | 45 | a0001c0001t0001g0184a0001c0001t0001g0259a0002c0002t0002g0002others(42): Show | 55 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.-9-1226C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121300737 | ||||||
chr9:121300960
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-9-1003G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121300960 | ||||||
chr9:121300979
|
C | A | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-984C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121300979 | ||||||
chr9:121301032
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-9-931C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301032 | ||||||
chr9:121301036
|
C | T | 2 | a0001c0003t0001g0016a0001c0003t0001g0100 | 3 | NA18971.hp2 NA18988.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-9-927C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301036 | ||||||
chr9:121301046
|
C | T | 1 | a0001c0001t0001g0023 | 2 | HG02083.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-9-917C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301046 | ||||||
chr9:121301074
|
G | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-9-889G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301074 | ||||||
chr9:121301346
|
G | C | 5 | a0001c0001t0001g0184a0001c0001t0001g0259a0004c0006t0004g0257others(2): Show | 5 | HG02109.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-617G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301346 | ||||||
chr9:121301352
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0122others(4): Show | 8 | HG01106.hp1 HG01243.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-611C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301352 | ||||||
chr9:121301429
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(3): Show | 9 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-534C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301429 | ||||||
chr9:121301493
|
T | G | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-9-470T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301493 | ||||||
chr9:121301550
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(3): Show | 9 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-413C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301550 | ||||||
chr9:121301574
|
C | T | 1 | a0004c0006t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-389C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301574 | ||||||
chr9:121301625
|
C | CA | 15 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0036others(12): Show | 18 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-319dupA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121301625 | |||||
chr9:121301625
|
CA | C | 19 | a0001c0001t0001g0041a0001c0001t0001g0084a0001c0001t0001g0107others(16): Show | 21 | HG00323.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9-319delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121301625 | |||||
chr9:121301625
|
CAAAAAAA | C | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 11 | HG02280.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-325_-9-319delAA others(5): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121301625 | |||||
chr9:121301639
|
A | G | 38 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(35): Show | 47 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9-324A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301639 | ||||||
chr9:121301640
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-9-323A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301640 | ||||||
chr9:121301778
|
C | G | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 11 | HG02280.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-185C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301778 | ||||||
chr9:121301877
|
G | C | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-86G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301877 | ||||||
chr9:121301932
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-9-31C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301932 | ||||||
chr9:121302322
|
C | A | 1 | a0002c0015t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.196+155C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302322 | ||||||
chr9:121302356
|
C | T | 4 | a0001c0003t0001g0203a0001c0003t0001g0213a0001c0003t0001g0214others(1): Show | 4 | HG02965.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+189C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302356 | ||||||
chr9:121302501
|
C | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0186a0001c0001t0001g0188 | 6 | HG02055.hp1 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+334C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302501 | ||||||
chr9:121302520
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196+353C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302520 | ||||||
chr9:121302570
|
TG | T | 3 | a0004c0006t0004g0224a0004c0006t0004g0225a0004c0006t0004g0240 | 3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.197-340delG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302570 | ||||||
chr9:121302572
|
C | A | 3 | a0004c0006t0004g0224a0004c0006t0004g0225a0004c0006t0004g0240 | 3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.197-339C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302572 | ||||||
chr9:121302585
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(3): Show | 9 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-326G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302585 | ||||||
chr9:121302650
|
G | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.197-261G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302650 | ||||||
chr9:121302670
|
G | C | 2 | a0001c0010t0001g0114a0001c0010t0001g0115 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.197-241G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302670 | ||||||
chr9:121302685
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.197-226G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302685 | ||||||
chr9:121302746
|
G | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0186a0001c0001t0001g0188 | 6 | HG02055.hp1 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-165G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302746 | ||||||
chr9:121302906
|
C | T | 1 | a0001c0003t0001g0214 | 1 | HG03516.hp1 | splice_region_variant&intron_variant | LOW | c.197-5C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302906 | ||||||
chr9:121303138
|
A | G | 2 | a0001c0010t0001g0114a0001c0010t0001g0115 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.351+73A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303138 | ||||||
chr9:121303238
|
G | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0249others(2): Show | 5 | HG01074.hp1 HG02148.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+173G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303238 | ||||||
chr9:121303411
|
G | A | 1 | a0001c0003t0001g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.351+346G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303411 | ||||||
chr9:121303443
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.351+378C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303443 | ||||||
chr9:121303456
|
C | T | 1 | a0001c0001t0003g0152 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.351+391C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303456 | ||||||
chr9:121303764
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.351+699C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303764 | ||||||
chr9:121304038
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.351+973A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304038 | ||||||
chr9:121304222
|
CAGAT | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+1160_351+1163d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr9 | 121304222 | |||||
chr9:121304228
|
G | A | 2 | a0001c0003t0001g0016a0001c0003t0001g0100 | 3 | NA18971.hp2 NA18988.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.351+1163G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304228 | ||||||
chr9:121304375
|
T | C | 2 | a0001c0001t0001g0139a0001c0004t0002g0156 | 2 | HG00621.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.351+1310T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304375 | ||||||
chr9:121304572
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(4): Show | 10 | HG01109.hp1 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+1507G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304572 | ||||||
chr9:121304722
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.351+1657G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304722 | ||||||
chr9:121304936
|
C | T | 1 | a0001c0003t0001g0262 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.351+1871C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304936 | ||||||
chr9:121305053
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0229 | 2 | HG01175.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.351+1988A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305053 | ||||||
chr9:121305167
|
A | G | 1 | a0004c0006t0004g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+2102A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305167 | ||||||
chr9:121305234
|
A | G | 5 | a0003c0005t0001g0242a0003c0005t0001g0243a0003c0005t0001g0244others(2): Show | 5 | HG02451.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2169A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305234 | ||||||
chr9:121305483
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.351+2418A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305483 | ||||||
chr9:121305498
|
G | A | 1 | a0001c0003t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.351+2433G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305498 | ||||||
chr9:121305511
|
G | A | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(75): Show | 96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.351+2446G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305511 | ||||||
chr9:121305570
|
A | G | 1 | a0002c0015t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.351+2505A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305570 | ||||||
chr9:121305849
|
C | T | 1 | a0001c0003t0001g0262 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.351+2784C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305849 | ||||||
chr9:121306122
|
A | G | 1 | a0002c0015t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.351+3057A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306122 | ||||||
chr9:121306136
|
C | T | 6 | a0002c0002t0002g0013a0002c0002t0002g0053a0002c0002t0002g0071others(3): Show | 7 | HG00438.hp2 HG02071.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+3071C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306136 | ||||||
chr9:121306506
|
T | TATATATC | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(75): Show | 96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.351+3446_351+3447i others(9): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr9 | 121306506 | |||||
chr9:121306554
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0184others(11): Show | 17 | HG01109.hp1 HG01261.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.351+3489C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306554 | ||||||
chr9:121306844
|
A | T | 1 | a0001c0003t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.351+3779A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306844 | ||||||
chr9:121306879
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.352-3805C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306879 | ||||||
chr9:121307183
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.352-3501A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307183 | ||||||
chr9:121307243
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(84): Show | 107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.352-3441A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307243 | ||||||
chr9:121307310
|
T | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG00558.hp1 NA18942.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-3374T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307310 | ||||||
chr9:121307360
|
T | A | 1 | a0004c0006t0004g0224 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.352-3324T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307360 | ||||||
chr9:121307391
|
T | C | 1 | a0004c0006t0004g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.352-3293T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307391 | ||||||
chr9:121307537
|
A | G | 63 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(60): Show | 78 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.352-3147A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307537 | ||||||
chr9:121307545
|
C | T | 47 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(44): Show | 58 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.352-3139C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307545 | ||||||
chr9:121307758
|
G | C | 1 | a0001c0003t0001g0262 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.352-2926G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307758 | ||||||
chr9:121307780
|
C | T | 39 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0010others(36): Show | 48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.352-2904C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307780 | ||||||
chr9:121307787
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.352-2897G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307787 | ||||||
chr9:121307787
|
G | T | 1 | a0001c0003t0001g0262 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.352-2897G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307787 | ||||||
chr9:121307872
|
G | A | 1 | a0012c0019t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.352-2812G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307872 | ||||||
chr9:121307881
|
G | A | 1 | a0001c0003t0001g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-2803G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307881 | ||||||
chr9:121307954
|
G | A | 1 | a0013c0021t0001g0108 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.352-2730G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307954 | ||||||
chr9:121308246
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.352-2438C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308246 | ||||||
chr9:121308459
|
C | G | 1 | a0004c0006t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.352-2225C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308459 | ||||||
chr9:121308636
|
C | T | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.352-2048C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308636 | ||||||
chr9:121308792
|
G | C | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.352-1892G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308792 | ||||||
chr9:121308801
|
A | G | 1 | a0001c0023t0003g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.352-1883A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308801 | ||||||
chr9:121309054
|
G | A | 1 | a0001c0023t0003g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.352-1630G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309054 | ||||||
chr9:121309066
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(16): Show | 24 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.352-1618C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309066 | ||||||
chr9:121309113
|
G | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG00140.hp2 HG01261.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.352-1571G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309113 | ||||||
chr9:121309180
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.352-1504A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309180 | ||||||
chr9:121309237
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.352-1447G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309237 | ||||||
chr9:121309307
|
A | T | 1 | a0001c0001t0001g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.352-1377A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309307 | ||||||
chr9:121309332
|
C | T | 1 | a0001c0003t0001g0262 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.352-1352C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309332 | ||||||
chr9:121309466
|
G | A | 40 | a0001c0001t0001g0022a0001c0001t0001g0023a0002c0002t0002g0002others(37): Show | 51 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.352-1218G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309466 | ||||||
chr9:121309843
|
T | TTACTTAG others(10): Show |
1 | a0001c0003t0001g0151 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.352-841_352-840ins others(17): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309843 | ||||||
chr9:121309849
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(67): Show | 86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.352-835C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309849 | ||||||
chr9:121309915
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.352-769T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309915 | ||||||
chr9:121309983
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.352-701C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309983 | ||||||
chr9:121309984
|
G | A | 1 | a0011c0020t0001g0258 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-700G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309984 | ||||||
chr9:121310015
|
A | G | 4 | a0001c0001t0003g0017a0001c0001t0003g0109a0001c0001t0003g0116others(1): Show | 5 | HG02145.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-669A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310015 | ||||||
chr9:121310134
|
A | G | 1 | a0001c0003t0001g0228 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-550A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310134 | ||||||
chr9:121310319
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(88): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.352-365C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310319 | ||||||
chr9:121310374
|
G | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.352-310G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310374 | ||||||
chr9:121310623
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.352-61T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310623 | ||||||
chr9:121310864
|
T | C | 2 | a0008c0011t0001g0040a0011c0020t0001g0258 | 3 | HG02717.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.513+19T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121310864 | ||||||
chr9:121310898
|
T | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(242): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.513+53T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121310898 | ||||||
chr9:121310968
|
G | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0212 | 3 | NA18993.hp2 NA19012.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.513+123G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121310968 | ||||||
chr9:121311025
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG00621.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.513+180G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311025 | ||||||
chr9:121311128
|
C | T | 1 | a0007c0018t0001g0091 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.513+283C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311128 | ||||||
chr9:121311138
|
C | A | 1 | a0001c0001t0001g0252 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.513+293C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311138 | ||||||
chr9:121311275
|
G | A | 242 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.513+430G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311275 | ||||||
chr9:121311324
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.513+479C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311324 | ||||||
chr9:121311330
|
G | C | 1 | a0001c0004t0002g0044 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.513+485G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311330 | ||||||
chr9:121311567
|
T | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.513+722T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311567 | ||||||
chr9:121311981
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.514-358G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311981 | ||||||
chr9:121312131
|
C | G | 1 | a0002c0002t0002g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.514-208C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121312131 | ||||||
chr9:121312142
|
G | A | 242 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.514-197G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121312142 | ||||||
chr9:121312513
|
T | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.663+25T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312513 | ||||||
chr9:121312594
|
C | T | 5 | a0001c0001t0001g0148a0001c0001t0001g0222a0001c0010t0001g0114others(2): Show | 5 | HG00609.hp2 HG01109.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.663+106C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312594 | ||||||
chr9:121312684
|
G | T | 1 | a0001c0023t0003g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.663+196G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312684 | ||||||
chr9:121312687
|
G | C | 133 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.663+199G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312687 | ||||||
chr9:121312753
|
G | A | 3 | a0001c0001t0001g0118a0001c0004t0002g0044a0001c0004t0002g0045 | 3 | HG01993.hp1 HG02300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.663+265G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312753 | ||||||
chr9:121312788
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.663+300A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312788 | ||||||
chr9:121312865
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.663+377C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312865 | ||||||
chr9:121312976
|
G | A | 133 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.663+488G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312976 | ||||||
chr9:121312981
|
G | A | 82 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(79): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.663+493G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312981 | ||||||
chr9:121313007
|
C | A | 242 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.663+519C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313007 | ||||||
chr9:121313132
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.663+644C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313132 | ||||||
chr9:121313266
|
G | A | 133 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.664-668G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313266 | ||||||
chr9:121313514
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.664-420T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313514 | ||||||
chr9:121313594
|
G | C | 2 | a0001c0010t0001g0114a0001c0010t0001g0115 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.664-340G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313594 | ||||||
chr9:121313625
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.664-309G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313625 | ||||||
chr9:121313671
|
C | T | 1 | a0002c0002t0007g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.664-263C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313671 | ||||||
chr9:121313698
|
C | T | 7 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(4): Show | 8 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.664-236C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313698 | ||||||
chr9:121313738
|
G | A | 133 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.664-196G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313738 | ||||||
chr9:121313888
|
C | A | 1 | a0012c0019t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.664-46C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313888 | ||||||
chr9:121313930
|
A | G | 1 | a0012c0019t0001g0232 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.664-4A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313930 | ||||||
chr9:121314054
|
A | C | 1 | a0001c0001t0001g0199 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.753+31A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314054 | ||||||
chr9:121314125
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.753+102C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314125 | ||||||
chr9:121314316
|
A | T | 1 | a0001c0001t0001g0105 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.753+293A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314316 | ||||||
chr9:121314326
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.753+303G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314326 | ||||||
chr9:121314367
|
T | C | 1 | a0001c0003t0001g0100 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.753+344T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314367 | ||||||
chr9:121314389
|
G | A | 1 | a0001c0023t0003g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.753+366G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314389 | ||||||
chr9:121314538
|
C | T | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.753+515C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314538 | ||||||
chr9:121315009
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 139 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.753+986C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315009 | ||||||
chr9:121315142
|
T | C | 2 | a0004c0006t0004g0185a0004c0006t0004g0257 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.753+1119T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315142 | ||||||
chr9:121315446
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.753+1423C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315446 | ||||||
chr9:121315447
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.753+1424G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315447 | ||||||
chr9:121315505
|
T | C | 1 | a0002c0002t0007g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.753+1482T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315505 | ||||||
chr9:121315518
|
C | T | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.753+1495C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315518 | ||||||
chr9:121315562
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.754-1524G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315562 | ||||||
chr9:121315725
|
C | T | 44 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(41): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.754-1361C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315725 | ||||||
chr9:121315767
|
T | A | 70 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(67): Show | 86 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.754-1319T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315767 | ||||||
chr9:121316094
|
T | G | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.754-992T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316094 | ||||||
chr9:121316295
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.754-791G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316295 | ||||||
chr9:121316531
|
C | T | 44 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(41): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.754-555C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316531 | ||||||
chr9:121316660
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.754-426G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316660 | ||||||
chr9:121316682
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.754-404G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316682 | ||||||
chr9:121316700
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.754-386G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316700 | ||||||
chr9:121316814
|
A | G | 1 | a0007c0018t0001g0091 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.754-272A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316814 | ||||||
chr9:121316832
|
C | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.754-254C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316832 | ||||||
chr9:121316959
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.754-127C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316959 | ||||||
chr9:121317237
|
G | T | 1 | a0001c0001t0001g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.886+19G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317237 | ||||||
chr9:121317253
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.886+35G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317253 | ||||||
chr9:121317523
|
T | C | 56 | a0001c0001t0001g0041a0001c0001t0001g0263a0001c0001t0003g0152others(53): Show | 68 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.886+305T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317523 | ||||||
chr9:121317569
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.886+351C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317569 | ||||||
chr9:121317766
|
C | G | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.886+548C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317766 | ||||||
chr9:121317995
|
G | A | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.887-411G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317995 | ||||||
chr9:121318075
|
C | CCTTATAG others(21): Show |
1 | a0001c0001t0001g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.887-327_887-300dup others(28): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 121318075 | |||||
chr9:121318075
|
C | T | 1 | a0001c0003t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.887-331C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121318075 | ||||||
chr9:121318096
|
G | C | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.887-310G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121318096 | ||||||
chr9:121318279
|
G | C | 2 | a0001c0010t0001g0114a0001c0010t0001g0115 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.887-127G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121318279 | ||||||
chr9:121318365
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0186a0001c0001t0001g0188 | 6 | HG02055.hp1 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.887-41C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121318365 | ||||||
chr9:121318537
|
G | C | 19 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0085others(16): Show | 21 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.975+43G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 9/17 | chr9 | 121318537 | ||||||
chr9:121318547
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.975+53G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 9/17 | chr9 | 121318547 | ||||||
chr9:121318558
|
G | A | 2 | a0004c0006t0004g0185a0004c0006t0004g0257 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.975+64G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 9/17 | chr9 | 121318558 | ||||||
chr9:121318916
|
C | T | 1 | a0014c0017t0001g0090 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1191+36C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121318916 | ||||||
chr9:121318985
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0031others(9): Show | 16 | HG02523.hp2 NA18944.hp1 NA18953.hp1 others(13): Show |
intron_variant | MODIFIER | c.1191+105T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121318985 | ||||||
chr9:121319487
|
C | CT | 12 | a0001c0001t0001g0147a0001c0010t0001g0114a0001c0010t0001g0115others(9): Show | 13 | HG01109.hp1 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1191+622dupT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 121319487 | |||||
chr9:121319548
|
C | G | 1 | a0001c0003t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1191+668C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121319548 | ||||||
chr9:121319551
|
G | C | 39 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(36): Show | 48 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1191+671G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121319551 | ||||||
chr9:121319791
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1191+911A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121319791 | ||||||
chr9:121320074
|
G | C | 3 | a0004c0006t0004g0224a0004c0006t0004g0225a0004c0006t0004g0240 | 3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1191+1194G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320074 | ||||||
chr9:121320106
|
T | C | 1 | a0001c0010t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1192-1162T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320106 | ||||||
chr9:121320205
|
C | T | 1 | a0012c0019t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1192-1063C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320205 | ||||||
chr9:121320537
|
C | T | 1 | a0001c0023t0003g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1192-731C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320537 | ||||||
chr9:121320652
|
CA | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0194a0001c0001t0001g0235others(3): Show | 6 | HG01070.hp1 HG02896.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1192-602delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 121320652 | |||||
chr9:121320652
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0004t0002g0156 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1192-611_1192-602d others(12): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 121320652 | |||||
chr9:121320687
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0104a0001c0001t0001g0110others(3): Show | 7 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1192-581G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320687 | ||||||
chr9:121320806
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1192-462T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320806 | ||||||
chr9:121320897
|
G | A | 23 | a0001c0003t0001g0001a0001c0003t0001g0009a0001c0003t0001g0016others(20): Show | 30 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1192-371G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320897 | ||||||
chr9:121321142
|
G | A | 27 | a0001c0001t0001g0032a0001c0003t0001g0001a0001c0003t0001g0009others(24): Show | 35 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1192-126G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121321142 | ||||||
chr9:121321193
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(14): Show | 22 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1192-75C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121321193 | ||||||
chr9:121321207
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1192-61C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121321207 | ||||||
chr9:121321484
|
G | A | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1325+83G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321484 | ||||||
chr9:121321542
|
C | A | 1 | a0002c0002t0002g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1325+141C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321542 | ||||||
chr9:121321565
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1325+164A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321565 | ||||||
chr9:121321594
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1325+193T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321594 | ||||||
chr9:121321636
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1325+235A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321636 | ||||||
chr9:121321670
|
A | G | 23 | a0001c0003t0001g0001a0001c0003t0001g0009a0001c0003t0001g0016others(20): Show | 30 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1325+269A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321670 | ||||||
chr9:121321731
|
G | GTTTA | 3 | a0001c0001t0001g0154a0001c0001t0001g0164a0001c0001t0001g0168 | 3 | HG00140.hp2 HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1325+354_1325+357d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121321731 | |||||
chr9:121321731
|
GTTTA | G | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(117): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1325+354_1325+357d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121321731 | |||||
chr9:121321757
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1325+356T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321757 | ||||||
chr9:121321762
|
G | A | 42 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(39): Show | 52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1325+361G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321762 | ||||||
chr9:121321812
|
G | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1325+411G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321812 | ||||||
chr9:121321825
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1325+424T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321825 | ||||||
chr9:121321842
|
A | G | 1 | a0001c0003t0001g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1325+441A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321842 | ||||||
chr9:121321861
|
CCT | C | 3 | a0004c0006t0004g0224a0004c0006t0004g0225a0004c0006t0004g0240 | 3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1325+465_1325+466d others(4): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121321861 | |||||
chr9:121321916
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1325+515T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321916 | ||||||
chr9:121322133
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1325+732C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322133 | ||||||
chr9:121322192
|
C | G | 3 | a0004c0006t0004g0224a0004c0006t0004g0225a0004c0006t0004g0240 | 3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1325+791C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322192 | ||||||
chr9:121322205
|
TTCCAGTA others(44): Show |
T | 1 | a0001c0001t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1325+805_1325+855d others(53): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322205 | ||||||
chr9:121322306
|
C | A | 2 | a0001c0001t0001g0032a0001c0023t0003g0043 | 3 | HG00639.hp2 HG00735.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1325+905C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322306 | ||||||
chr9:121322330
|
T | G | 1 | a0001c0001t0001g0204 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1325+929T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322330 | ||||||
chr9:121322335
|
A | G | 1 | a0001c0003t0001g0214 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1325+934A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322335 | ||||||
chr9:121322667
|
C | A | 1 | a0001c0001t0001g0165 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1325+1266C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322667 | ||||||
chr9:121322702
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1325+1301G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322702 | ||||||
chr9:121322733
|
G | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1325+1332G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322733 | ||||||
chr9:121322783
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0136 | 3 | HG01106.hp2 HG01192.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1325+1382T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322783 | ||||||
chr9:121322807
|
CT | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0122a0001c0001t0001g0235 | 3 | HG01070.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1325+1411delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121322807 | |||||
chr9:121322833
|
A | AT | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1325+1447dupT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121322833 | |||||
chr9:121322871
|
G | C | 42 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(39): Show | 52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1325+1470G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322871 | ||||||
chr9:121322912
|
C | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0124others(8): Show | 15 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1325+1511C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322912 | ||||||
chr9:121322993
|
A | G | 247 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(244): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1326-1561A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322993 | ||||||
chr9:121323036
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1326-1518T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323036 | ||||||
chr9:121323055
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0136 | 3 | HG01106.hp2 HG01192.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1326-1499G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323055 | ||||||
chr9:121323122
|
C | T | 1 | a0012c0019t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1326-1432C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323122 | ||||||
chr9:121323205
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 20 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1326-1349C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323205 | ||||||
chr9:121323229
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1326-1325A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323229 | ||||||
chr9:121323284
|
A | C | 3 | a0004c0006t0004g0224a0004c0006t0004g0225a0004c0006t0004g0240 | 3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1326-1270A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323284 | ||||||
chr9:121323371
|
G | GTTTTT | 114 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(111): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1326-1169_1326-116 others(9): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121323371 | |||||
chr9:121323371
|
G | GTTTTTT | 30 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0018others(27): Show | 38 | HG00597.hp2 HG01106.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1326-1170_1326-116 others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121323371 | |||||
chr9:121323400
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1326-1154T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323400 | ||||||
chr9:121323440
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0183a0001c0001t0001g0186others(2): Show | 8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1326-1114G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323440 | ||||||
chr9:121323450
|
A | G | 1 | a0004c0006t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1326-1104A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323450 | ||||||
chr9:121323562
|
GT | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1326-989delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121323562 | |||||
chr9:121323768
|
C | T | 13 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0105others(10): Show | 14 | HG01074.hp1 HG02145.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.1326-786C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323768 | ||||||
chr9:121323874
|
A | T | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1326-680A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323874 | ||||||
chr9:121324015
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0146a0001c0001t0001g0176 | 3 | HG02155.hp2 NA18971.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1326-539A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121324015 | ||||||
chr9:121324056
|
A | T | 3 | a0001c0001t0001g0118a0009c0012t0001g0098a0009c0012t0001g0102 | 3 | HG02451.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1326-498A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121324056 | ||||||
chr9:121324298
|
A | C | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1326-256A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121324298 | ||||||
chr9:121324415
|
G | C | 1 | a0001c0003t0001g0205 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1326-139G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121324415 | ||||||
chr9:121324438
|
CTCTA | C | 3 | a0004c0006t0004g0224a0004c0006t0004g0225a0004c0006t0004g0240 | 3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1326-112_1326-109d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121324438 | |||||
chr9:121324739
|
ATCTG | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1416+106_1416+109d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324739 | |||||
chr9:121324751
|
G | GTCCA | 37 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0021others(34): Show | 46 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1416+149_1416+152d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | |||||
chr9:121324751
|
G | GTCCATCC others(1): Show |
6 | a0001c0001t0001g0042a0001c0001t0001g0153a0001c0001t0001g0176others(3): Show | 6 | HG01243.hp1 HG01256.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1416+145_1416+152d others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | |||||
chr9:121324751
|
G | GTCCATCC others(9): Show |
1 | a0001c0001t0001g0167 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1416+137_1416+152d others(18): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | |||||
chr9:121324751
|
GTCCA | G | 4 | a0001c0001t0001g0082a0004c0006t0004g0224a0004c0006t0004g0225others(1): Show | 4 | HG01071.hp2 HG02738.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416+149_1416+152d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | |||||
chr9:121324751
|
GTCCATCC others(1): Show |
G | 4 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0001g0158others(1): Show | 4 | HG01934.hp2 HG02738.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1416+145_1416+152d others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | |||||
chr9:121324755
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1416+111A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121324755 | ||||||
chr9:121324776
|
T | C | 42 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(39): Show | 52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1416+132T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121324776 | ||||||
chr9:121324835
|
C | T | 38 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(35): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1416+191C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121324835 | ||||||
chr9:121325087
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1416+443T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325087 | ||||||
chr9:121325349
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1416+705A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325349 | ||||||
chr9:121325388
|
C | T | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1416+744C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325388 | ||||||
chr9:121325637
|
C | T | 239 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(236): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1417-875C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325637 | ||||||
chr9:121325656
|
C | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1417-856C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325656 | ||||||
chr9:121325715
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1417-797A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325715 | ||||||
chr9:121325842
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1417-670C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325842 | ||||||
chr9:121325890
|
C | G | 1 | a0001c0001t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1417-622C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325890 | ||||||
chr9:121325899
|
G | A | 1 | a0002c0007t0001g0056 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1417-613G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325899 | ||||||
chr9:121325929
|
T | C | 239 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(236): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1417-583T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325929 | ||||||
chr9:121325948
|
G | A | 1 | a0002c0002t0002g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1417-564G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325948 | ||||||
chr9:121325961
|
C | T | 3 | a0002c0002t0002g0064a0002c0002t0002g0069a0002c0002t0002g0077 | 3 | NA18612.hp1 NA19003.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1417-551C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325961 | ||||||
chr9:121325962
|
A | G | 42 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(39): Show | 52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1417-550A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325962 | ||||||
chr9:121326081
|
C | T | 25 | a0001c0001t0001g0032a0001c0003t0001g0001a0001c0003t0001g0009others(22): Show | 33 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1417-431C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326081 | ||||||
chr9:121326160
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1417-352G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326160 | ||||||
chr9:121326177
|
A | C | 42 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(39): Show | 52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1417-335A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326177 | ||||||
chr9:121326256
|
C | G | 1 | a0002c0014t0002g0048 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1417-256C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326256 | ||||||
chr9:121326453
|
A | G | 49 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(46): Show | 60 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1417-59A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326453 | ||||||
chr9:121326462
|
C | A | 2 | a0004c0006t0004g0225a0004c0006t0004g0240 | 2 | HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1417-50C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326462 | ||||||
chr9:121326490
|
T | C | 248 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1417-22T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326490 | ||||||
chr9:121326491
|
G | A | 1 | a0010c0013t0001g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1417-21G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326491 | ||||||
chr9:121326728
|
A | G | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+46A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326728 | ||||||
chr9:121326760
|
C | T | 1 | a0001c0004t0002g0172 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1587+78C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326760 | ||||||
chr9:121326774
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1587+92G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326774 | ||||||
chr9:121326894
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1587+212A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326894 | ||||||
chr9:121326895
|
C | T | 239 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(236): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1587+213C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326895 | ||||||
chr9:121327186
|
T | C | 2 | a0001c0010t0001g0114a0001c0010t0001g0115 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1588-122T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121327186 | ||||||
chr9:121327230
|
GC | G | 38 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(35): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1588-77delC | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121327230 | ||||||
chr9:121327231
|
C | T | 4 | a0002c0002t0004g0054a0002c0002t0004g0055a0006c0009t0004g0037others(1): Show | 5 | HG02572.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1588-77C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121327231 | ||||||
chr9:121327232
|
G | T | 38 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(35): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1588-76G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121327232 | ||||||
chr9:121327566
|
A | C | 4 | a0002c0002t0004g0054a0002c0002t0004g0055a0006c0009t0004g0037others(1): Show | 5 | HG02572.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1762+84A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327566 | ||||||
chr9:121327716
|
G | GTAATCCC others(128): Show |
9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1762+245_1762+379d others(137): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 121327716 | |||||
chr9:121327740
|
A | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(14): Show | 22 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1762+258A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327740 | ||||||
chr9:121327828
|
C | T | 6 | a0004c0006t0004g0185a0004c0006t0004g0224a0004c0006t0004g0225others(3): Show | 6 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1762+346C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327828 | ||||||
chr9:121327833
|
A | G | 1 | a0002c0002t0002g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1762+351A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327833 | ||||||
chr9:121327845
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(72): Show | 93 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1762+363G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327845 | ||||||
chr9:121327846
|
C | T | 6 | a0004c0006t0004g0185a0004c0006t0004g0224a0004c0006t0004g0225others(3): Show | 6 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1762+364C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327846 | ||||||
chr9:121327904
|
T | G | 250 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1762+422T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327904 | ||||||
chr9:121327955
|
C | T | 42 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(39): Show | 52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1762+473C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327955 | ||||||
chr9:121327980
|
G | GAAGA | 3 | a0001c0001t0001g0041a0001c0001t0001g0171a0001c0001t0001g0263 | 4 | HG02976.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762+514_1762+517d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 121327980 | |||||
chr9:121328060
|
G | GC | 17 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(14): Show | 22 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1762+580dupC | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 121328060 | |||||
chr9:121328083
|
C | G | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1762+601C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328083 | ||||||
chr9:121328180
|
C | T | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1762+698C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328180 | ||||||
chr9:121328202
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1763-689G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328202 | ||||||
chr9:121328237
|
C | A | 1 | a0004c0006t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1763-654C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328237 | ||||||
chr9:121328344
|
T | TTGTGTTT others(44): Show |
1 | a0001c0001t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1763-546_1763-545i others(53): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 121328344 | |||||
chr9:121328346
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1763-545T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328346 | ||||||
chr9:121328367
|
G | A | 42 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(39): Show | 52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1763-524G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328367 | ||||||
chr9:121328500
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1763-391A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328500 | ||||||
chr9:121328506
|
G | A | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(238): Show | 293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1763-385G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328506 | ||||||
chr9:121328521
|
G | T | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1763-370G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328521 | ||||||
chr9:121328715
|
C | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0138a0001c0001t0001g0167others(1): Show | 4 | NA18747.hp2 NA18975.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1763-176C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328715 | ||||||
chr9:121328777
|
G | A | 1 | a0002c0015t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1763-114G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328777 | ||||||
chr9:121328857
|
G | A | 239 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(236): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1763-34G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328857 | ||||||
chr9:121329061
|
G | T | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1887+46G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 15/17 | chr9 | 121329061 | ||||||
chr9:121329201
|
G | GAAGACAT others(4): Show |
1 | a0002c0002t0002g0255 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1888-36_1888-26dup others(11): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr9 | 121329201 | |||||
chr9:121329459
|
C | T | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1965+144C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329459 | ||||||
chr9:121329507
|
G | A | 21 | a0001c0003t0001g0001a0001c0003t0001g0009a0001c0003t0001g0016others(18): Show | 28 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.1965+192G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329507 | ||||||
chr9:121329507
|
G | C | 2 | a0004c0006t0004g0185a0004c0006t0004g0257 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1965+192G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329507 | ||||||
chr9:121329705
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1965+390G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329705 | ||||||
chr9:121329706
|
G | A | 4 | a0002c0002t0004g0054a0002c0002t0004g0055a0006c0009t0004g0037others(1): Show | 5 | HG02572.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1965+391G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329706 | ||||||
chr9:121329728
|
C | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0263 | 3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1965+413C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329728 | ||||||
chr9:121329771
|
T | G | 1 | a0008c0011t0001g0040 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1965+456T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329771 | ||||||
chr9:121329983
|
C | T | 52 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(49): Show | 64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1965+668C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329983 | ||||||
chr9:121330077
|
C | T | 65 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(62): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1965+762C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330077 | ||||||
chr9:121330107
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1965+792A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330107 | ||||||
chr9:121330139
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1965+824G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330139 | ||||||
chr9:121330467
|
T | C | 52 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(49): Show | 64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1966-921T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330467 | ||||||
chr9:121330560
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1966-828G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330560 | ||||||
chr9:121330593
|
T | C | 54 | a0001c0001t0001g0041a0001c0001t0001g0263a0001c0004t0002g0044others(51): Show | 67 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1966-795T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330593 | ||||||
chr9:121331121
|
G | C | 1 | a0001c0001t0003g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1966-267G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121331121 | ||||||
chr9:121331213
|
T | A | 1 | a0001c0001t0001g0254 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1966-175T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121331213 | ||||||
chr9:121331484
|
T | C | 52 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(49): Show | 64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2026+36T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331484 | ||||||
chr9:121331535
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2026+87G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331535 | ||||||
chr9:121331662
|
A | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.2026+214A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331662 | ||||||
chr9:121331663
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2026+215A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331663 | ||||||
chr9:121331719
|
G | C | 5 | a0004c0006t0004g0185a0004c0006t0004g0224a0004c0006t0004g0225others(2): Show | 5 | HG01071.hp2 HG01884.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2026+271G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331719 | ||||||
chr9:121331736
|
A | G | 249 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(246): Show | 302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.2026+288A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331736 | ||||||
chr9:121331747
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2026+299G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331747 | ||||||
chr9:121331870
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2026+422A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331870 | ||||||
chr9:121331881
|
T | C | 52 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(49): Show | 64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2026+433T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331881 | ||||||
chr9:121331973
|
T | C | 9 | a0003c0005t0001g0038a0003c0005t0001g0242a0003c0005t0001g0243others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2027-461T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331973 | ||||||
chr9:121332012
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0164 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.2027-422C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121332012 | ||||||
chr9:121332157
|
T | C | 50 | a0001c0004t0002g0044a0001c0004t0002g0045a0001c0004t0002g0123others(47): Show | 62 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.2027-277T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121332157 | ||||||
chr9:121332312
|
A | T | 42 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0035others(39): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2027-122A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121332312 | ||||||
chr9:121332402
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2027-32G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121332402 |