geneid | 51608 |
---|---|
ensemblid | ENSG00000239857.7 |
hgncid | 21690 |
symbol | GET4 |
name | guided entry of tail-anchored proteins factor 4 |
refseq_nuc | NM_015949.3 |
refseq_prot | NP_057033.2 |
ensembl_nuc | ENST00000265857.8 |
ensembl_prot | ENSP00000265857.3 |
mane_status | MANE Select |
chr | chr7 |
start | 876554 |
end | 896436 |
strand | + |
ver | v1.2 |
region | chr7:876554-896436 |
region5000 | chr7:871554-901436 |
regionname0 | GET4_chr7_876554_896436 |
regionname5000 | GET4_chr7_871554_901436 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 327 | 380 | 90 | 73 | 163 | 14 | 38 | 117 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0002 | 0/0 | 327 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0003 | 0/0 | 327 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 984 | 237 | 53 | 44 | 107 | 8 | 24 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0002 | 0/0 | 984 | 86 | 5 | 12 | 55 | 4 | 10 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0003 | 0/0 | 984 | 19 | 6 | 10 | 0 | 1 | 2 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0004 | 0/0 | 984 | 9 | 9 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0005 | 0/0 | 984 | 5 | 3 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0006 | 0/0 | 984 | 5 | 4 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0007 | 0/0 | 984 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0008 | 0/0 | 984 | 3 | 0 | 2 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0009 | 0/1 | 984 | 3 | 0 | 0 | 0 | 1 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0010 | 0/0 | 984 | 3 | 3 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0011 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0012 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0013 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0014 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0015 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0016 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0017 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0018 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0019 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0020 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
c0021 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1107 | 197 | 34 | 42 | 86 | 9 | 25 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0002 | 1/0 | 1107 | 105 | 28 | 24 | 39 | 2 | 11 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0003 | 0/0 | 1107 | 22 | 0 | 0 | 22 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0004 | 0/0 | 1107 | 9 | 8 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0005 | 0/0 | 1107 | 5 | 0 | 2 | 0 | 3 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0006 | 0/0 | 1107 | 3 | 2 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0007 | 0/0 | 1107 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0008 | 0/0 | 1107 | 2 | 1 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0009 | 0/0 | 1107 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0010 | 0/0 | 1107 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0011 | 0/0 | 1107 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0012 | 0/0 | 1107 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0013 | 0/0 | 1107 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0014 | 0/0 | 1107 | 2 | 1 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0015 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0016 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0017 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0018 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0019 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0020 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0021 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0022 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0023 | 0/0 | 1107 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0024 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0025 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0026 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0027 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0028 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0029 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0030 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0031 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0032 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0033 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0034 | 0/0 | 1107 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0035 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0036 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0037 | 0/0 | 1107 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0038 | 0/0 | 1107 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0039 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0040 | 0/0 | 1107 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
t0041 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 0 | 1 | 8 | 0 | 3 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0003 | 1/0 | 8 | 0 | 1 | 0 | 2 | 4 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0009 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0010 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0042 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 984 | 237 | 53 | 44 | 107 | 8 | 24 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002 | 0/0 | 984 | 86 | 5 | 12 | 55 | 4 | 10 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0003 | 0/0 | 984 | 19 | 6 | 10 | 0 | 1 | 2 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0004 | 0/0 | 984 | 9 | 9 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0005 | 0/0 | 984 | 5 | 3 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0006 | 0/0 | 984 | 5 | 4 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0008 | 0/0 | 984 | 3 | 0 | 2 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0009 | 0/1 | 984 | 3 | 0 | 0 | 0 | 1 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0010 | 0/0 | 984 | 3 | 3 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0011 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0012 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0013 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0014 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0015 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0016 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0017 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0019 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0020 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0021 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0002c0007 | 0/0 | 984 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0003c0018 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2090 | 155 | 29 | 35 | 66 | 7 | 18 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0002 | 1/0 | 2090 | 37 | 9 | 5 | 16 | 1 | 5 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0003 | 0/0 | 2090 | 14 | 0 | 0 | 14 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0004 | 0/0 | 2090 | 6 | 5 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0005 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0008 | 0/0 | 2090 | 2 | 1 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0009 | 0/0 | 2090 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0010 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0012 | 0/0 | 2090 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0013 | 0/0 | 2090 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0014 | 0/0 | 2090 | 2 | 1 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0016 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0017 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0018 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0022 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0024 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0027 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0029 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0031 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0033 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0036 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0037 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0039 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0001t0041 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0001 | 0/0 | 2090 | 26 | 3 | 1 | 16 | 1 | 5 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0002 | 0/0 | 2090 | 38 | 2 | 9 | 23 | 0 | 4 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0003 | 0/0 | 2090 | 8 | 0 | 0 | 8 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0005 | 0/0 | 2090 | 4 | 0 | 1 | 0 | 3 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0006 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0007 | 0/0 | 2090 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0015 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0019 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0020 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0021 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0030 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0035 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0002t0038 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0003t0001 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0003t0002 | 0/0 | 2090 | 14 | 2 | 9 | 0 | 1 | 2 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0003t0006 | 0/0 | 2090 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0003t0010 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0003t0034 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0004t0002 | 0/0 | 2090 | 6 | 6 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0004t0004 | 0/0 | 2090 | 3 | 3 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0005t0001 | 0/0 | 2090 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0005t0011 | 0/0 | 2090 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0005t0040 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0006t0002 | 0/0 | 2090 | 4 | 4 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0006t0023 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0008t0001 | 0/0 | 2090 | 3 | 0 | 2 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0009t0001 | 0/1 | 2090 | 3 | 0 | 0 | 0 | 1 | 1 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0010t0025 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0010t0026 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0010t0028 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0011t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0012t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0013t0032 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0014t0001 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0015t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0016t0001 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0017t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0019t0001 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0020t0001 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0001c0021t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0002c0007t0001 | 0/0 | 2090 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
a0003c0018t0002 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | copy fasta | chr7 | 871554 | 901436 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 0 | 2 | 4 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0010 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0009g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0013g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0013g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0014g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0017g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0018g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0022g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0024g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0027g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0029g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0033g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0036g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0037g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0039g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0001t0041g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0005g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0005g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0015g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0019g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0020g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0021g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0030g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0035g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0002t0038g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0006g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0003t0034g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0004t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0004t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0004t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0004t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0004t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0004t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0004t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0004t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0005t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0005t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0005t0011g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0005t0011g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0005t0040g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0006t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0006t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0006t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0006t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0006t0023g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0008t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0008t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0008t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0009t0001g0042 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0009t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0010t0025g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0010t0026g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0010t0028g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0011t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0012t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0013t0032g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0014t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0015t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0016t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0017t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0019t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0020t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0001c0021t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0002c0007t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
a0003c0018t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0167 | EUR | GBR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00280 | hp1 | a0001 | c0003 | t0002 | g0270 | EUR | FIN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00280 | hp2 | a0001 | c0009 | t0001 | g0042 | EUR | FIN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0023 | EUR | FIN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0110 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00597 | hp2 | a0001 | c0001 | t0022 | g0225 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00621 | hp1 | a0001 | c0001 | t0016 | g0002 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00642 | hp2 | a0001 | c0002 | t0005 | g0023 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0250 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01069 | hp1 | a0001 | c0003 | t0002 | g0041 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01071 | hp1 | a0001 | c0003 | t0002 | g0041 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0104 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0269 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01081 | hp2 | a0001 | c0006 | t0023 | g0266 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01106 | hp2 | a0001 | c0020 | t0001 | g0119 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01168 | hp2 | a0001 | c0008 | t0001 | g0274 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01175 | hp1 | a0001 | c0005 | t0001 | g0275 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01192 | hp1 | a0001 | c0001 | t0008 | g0182 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01243 | hp2 | a0001 | c0001 | t0014 | g0054 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01258 | hp2 | a0001 | c0005 | t0001 | g0273 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01261 | hp1 | a0001 | c0003 | t0034 | g0288 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01346 | hp2 | a0001 | c0008 | t0001 | g0272 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0113 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01496 | hp1 | a0001 | c0002 | t0006 | g0050 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01515 | hp1 | a0001 | c0002 | t0005 | g0024 | EUR | IBS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01517 | hp2 | a0001 | c0002 | t0005 | g0024 | EUR | IBS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01891 | hp1 | a0001 | c0005 | t0040 | g0265 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0284 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01943 | hp1 | a0003 | c0018 | t0002 | g0007 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0233 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01981 | hp1 | a0001 | c0003 | t0002 | g0285 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG01993 | hp2 | a0001 | c0003 | t0002 | g0287 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02004 | hp1 | a0001 | c0003 | t0002 | g0294 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02004 | hp2 | a0001 | c0003 | t0002 | g0286 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02055 | hp1 | a0001 | c0001 | t0012 | g0180 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0166 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02071 | hp1 | a0001 | c0001 | t0009 | g0178 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02083 | hp2 | a0001 | c0002 | t0035 | g0117 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02129 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02132 | hp1 | a0001 | c0002 | t0015 | g0135 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0111 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0188 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02148 | hp1 | a0001 | c0003 | t0002 | g0292 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02148 | hp2 | a0001 | c0019 | t0001 | g0126 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | CDX | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CDX | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02257 | hp1 | a0001 | c0001 | t0029 | g0192 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02258 | hp1 | a0001 | c0005 | t0011 | g0291 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02258 | hp2 | a0001 | c0021 | t0002 | g0097 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02280 | hp1 | a0001 | c0001 | t0012 | g0186 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02280 | hp2 | a0001 | c0001 | t0024 | g0187 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02451 | hp2 | a0001 | c0006 | t0002 | g0290 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02615 | hp1 | a0001 | c0017 | t0002 | g0049 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02647 | hp1 | a0001 | c0003 | t0006 | g0038 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02647 | hp2 | a0001 | c0003 | t0010 | g0168 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02698 | hp2 | a0001 | c0003 | t0002 | g0244 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0055 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02717 | hp2 | a0001 | c0003 | t0006 | g0038 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02723 | hp1 | a0001 | c0014 | t0001 | g0283 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02723 | hp2 | a0001 | c0010 | t0025 | g0053 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0121 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0092 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02896 | hp2 | a0001 | c0006 | t0002 | g0276 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02922 | hp1 | a0001 | c0012 | t0002 | g0014 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02965 | hp1 | a0001 | c0001 | t0036 | g0279 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02965 | hp2 | a0001 | c0004 | t0002 | g0040 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02970 | hp1 | a0001 | c0004 | t0002 | g0255 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03098 | hp2 | a0001 | c0010 | t0028 | g0051 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03130 | hp1 | a0001 | c0010 | t0026 | g0052 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03195 | hp1 | a0001 | c0004 | t0002 | g0040 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03209 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03225 | hp2 | a0001 | c0004 | t0002 | g0262 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03239 | hp1 | a0001 | c0009 | t0001 | g0268 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03453 | hp1 | a0001 | c0011 | t0002 | g0045 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0191 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03486 | hp2 | a0001 | c0004 | t0004 | g0260 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0101 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0099 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03516 | hp1 | a0001 | c0004 | t0004 | g0254 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03540 | hp2 | a0001 | c0006 | t0002 | g0267 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03579 | hp1 | a0001 | c0005 | t0011 | g0277 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0106 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03654 | hp2 | a0001 | c0001 | t0037 | g0213 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03834 | hp1 | a0001 | c0008 | t0001 | g0271 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0148 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG04115 | hp2 | a0001 | c0002 | t0038 | g0103 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0131 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0252 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18522 | hp1 | a0001 | c0015 | t0002 | g0096 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | CHB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | CHB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0094 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18948 | hp1 | a0001 | c0001 | t0013 | g0189 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18950 | hp2 | a0001 | c0002 | t0003 | g0095 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18951 | hp1 | a0001 | c0001 | t0041 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18952 | hp2 | a0001 | c0001 | t0031 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18954 | hp1 | a0002 | c0007 | t0001 | g0015 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18954 | hp2 | a0001 | c0002 | t0020 | g0098 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18959 | hp1 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18980 | hp2 | a0001 | c0001 | t0017 | g0020 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18994 | hp1 | a0001 | c0002 | t0007 | g0160 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19010 | hp1 | a0001 | c0001 | t0018 | g0060 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19011 | hp2 | a0001 | c0002 | t0021 | g0127 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0170 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19043 | hp2 | a0001 | c0004 | t0002 | g0256 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19058 | hp2 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19065 | hp1 | a0001 | c0002 | t0003 | g0128 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19067 | hp1 | a0002 | c0007 | t0001 | g0015 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19067 | hp2 | a0001 | c0001 | t0013 | g0194 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19070 | hp1 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19070 | hp2 | a0002 | c0007 | t0001 | g0015 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19079 | hp2 | a0001 | c0002 | t0019 | g0107 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19081 | hp2 | a0001 | c0002 | t0030 | g0007 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19088 | hp1 | a0001 | c0016 | t0001 | g0027 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19088 | hp2 | a0001 | c0002 | t0007 | g0143 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19090 | hp1 | a0001 | c0001 | t0039 | g0004 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19240 | hp1 | a0001 | c0003 | t0002 | g0046 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | ASW | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0122 | EUR | TSI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | GIH | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0116 | SAS | GIH | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02486 | hp1 | a0001 | c0006 | t0002 | g0289 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02559 | hp1 | a0001 | c0004 | t0004 | g0259 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03471 | hp1 | a0001 | c0004 | t0002 | g0257 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG03471 | hp2 | a0001 | c0013 | t0032 | g0014 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | USA | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
HG06807 | hp2 | a0001 | c0001 | t0027 | g0263 | AFR | USA | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | USA | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA21309 | hp1 | a0001 | c0001 | t0033 | g0091 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
homoSapiens_chm13v2 | hp1 | a0001 | c0009 | t0001 | g0042 | REF | REF | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0003 | REF | REF | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:876717
|
G | C | 1 | a0002 | 3 | NA18954.hp1 NA19067.hp1 NA19070.hp2 |
missense_variant | MODERATE | c.72G>C | p.Gln24His | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/9 | 164/2090 | 72/984 | 24/327 | chr7 | 876717 | ||
chr7:892322
|
C | T | 1 | a0003 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.650C>T | p.Thr217Met | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/9 | 742/2090 | 650/984 | 217/327 | chr7 | 892322 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:876699
|
C | T | 1 | a0001c0021 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.54C>T | p.Arg18Arg | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/9 | 146/2090 | 54/984 | 18/327 | chr7 | 876699 | ||
chr7:886080
|
G | A | 4 | a0001c0003a0001c0008a0001c0009others(1): Show | 26 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(23): Show |
synonymous_variant | LOW | c.180G>A | p.Thr60Thr | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/9 | 272/2090 | 180/984 | 60/327 | chr7 | 886080 | ||
chr7:886119
|
C | T | 1 | a0001c0020 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.219C>T | p.Phe73Phe | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/9 | 311/2090 | 219/984 | 73/327 | chr7 | 886119 | ||
chr7:890971
|
G | A | 4 | a0001c0005a0001c0006a0001c0008others(1): Show | 16 | HG00280.hp2 HG01081.hp2 HG01168.hp2 others(13): Show |
synonymous_variant | LOW | c.510G>A | p.Ala170Ala | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/9 | 602/2090 | 510/984 | 170/327 | chr7 | 890971 | ||
chr7:891052
|
C | T | 7 | a0001c0002a0001c0015a0001c0016others(4): Show | 92 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
synonymous_variant | LOW | c.591C>T | p.Ala197Ala | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/9 | 683/2090 | 591/984 | 197/327 | chr7 | 891052 | ||
chr7:892317
|
C | T | 1 | a0001c0019 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.645C>T | p.Val215Val | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/9 | 737/2090 | 645/984 | 215/327 | chr7 | 892317 | ||
chr7:892323
|
G | A | 6 | a0001c0005a0001c0006a0001c0008others(3): Show | 18 | HG01081.hp2 HG01168.hp2 HG01175.hp1 others(15): Show |
synonymous_variant | LOW | c.651G>A | p.Thr217Thr | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/9 | 743/2090 | 651/984 | 217/327 | chr7 | 892323 | ||
chr7:893904
|
C | G | 2 | a0001c0006a0001c0014 | 6 | HG01081.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.828C>G | p.Leu276Leu | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/9 | 920/2090 | 828/984 | 276/327 | chr7 | 893904 | ||
chr7:893958
|
C | T | 1 | a0001c0004 | 9 | HG02559.hp1 HG02965.hp2 HG02970.hp1 others(6): Show |
synonymous_variant | LOW | c.882C>T | p.Tyr294Tyr | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/9 | 974/2090 | 882/984 | 294/327 | chr7 | 893958 | ||
chr7:895362
|
C | T | 3 | a0001c0013a0001c0017a0001c0021 | 3 | HG02258.hp2 HG02615.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.924C>T | p.Ser308Ser | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1016/2090 | 924/984 | 308/327 | chr7 | 895362 | ||
chr7:895398
|
C | T | 1 | a0001c0016 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.960C>T | p.Asp320Asp | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1052/2090 | 960/984 | 320/327 | chr7 | 895398 | ||
chr7:895401
|
C | T | 1 | a0001c0012 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.963C>T | p.Gly321Gly | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1055/2090 | 963/984 | 321/327 | chr7 | 895401 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:876599
|
C | G | 1 | a0001c0001t0014 | 2 | HG01243.hp2 HG02717.hp1 |
5_prime_UTR_variant | MODIFIER | c.-47C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/9 | 47 | chr7 | 876599 | |||||
chr7:895446
|
C | T | 2 | a0001c0001t0013a0001c0001t0041 | 3 | NA18948.hp1 NA18951.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*24C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 24 | chr7 | 895446 | |||||
chr7:895449
|
C | T | 1 | a0001c0005t0040 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 27 | chr7 | 895449 | |||||
chr7:895450
|
G | A | 2 | a0001c0002t0007a0001c0002t0015 | 3 | HG02132.hp1 NA18994.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*28G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 28 | chr7 | 895450 | |||||
chr7:895459
|
C | T | 1 | a0001c0001t0039 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 37 | chr7 | 895459 | |||||
chr7:895483
|
G | A | 1 | a0001c0001t0016 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*61G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 61 | chr7 | 895483 | |||||
chr7:895569
|
C | T | 2 | a0001c0001t0004a0001c0004t0004 | 9 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*147C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 147 | chr7 | 895569 | |||||
chr7:895583
|
G | A | 7 | a0001c0001t0003a0001c0001t0017a0001c0001t0018others(4): Show | 27 | HG00558.hp1 HG02027.hp2 HG02071.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 161 | chr7 | 895583 | |||||
chr7:895584
|
C | T | 1 | a0001c0002t0038 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*162C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 162 | chr7 | 895584 | |||||
chr7:895585
|
G | A | 1 | a0001c0001t0022 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 163 | chr7 | 895585 | |||||
chr7:895627
|
C | T | 1 | a0001c0001t0037 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 205 | chr7 | 895627 | |||||
chr7:895640
|
C | T | 1 | a0001c0001t0036 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*218C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 218 | chr7 | 895640 | |||||
chr7:895669
|
A | G | 1 | a0001c0002t0035 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*247A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 247 | chr7 | 895669 | |||||
chr7:895748
|
A | T | 1 | a0001c0001t0012 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*326A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 326 | chr7 | 895748 | |||||
chr7:895757
|
G | A | 1 | a0001c0006t0023 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 335 | chr7 | 895757 | |||||
chr7:895792
|
G | A | 1 | a0001c0001t0024 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 370 | chr7 | 895792 | |||||
chr7:895795
|
C | T | 1 | a0001c0002t0021 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 373 | chr7 | 895795 | |||||
chr7:895836
|
C | A | 2 | a0001c0010t0025a0001c0010t0026 | 2 | HG02723.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 414 | chr7 | 895836 | |||||
chr7:895883
|
G | C | 3 | a0001c0001t0027a0001c0010t0025a0001c0010t0028 | 3 | HG02723.hp2 HG03098.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*461G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 461 | chr7 | 895883 | |||||
chr7:895907
|
T | C | 1 | a0001c0001t0029 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 485 | chr7 | 895907 | |||||
chr7:895942
|
G | A | 1 | a0001c0002t0007 | 2 | NA18994.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*520G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 520 | chr7 | 895942 | |||||
chr7:895989
|
C | T | 1 | a0001c0003t0034 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*567C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 567 | chr7 | 895989 | |||||
chr7:895997
|
G | C | 1 | a0001c0001t0012 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*575G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 575 | chr7 | 895997 | |||||
chr7:896052
|
G | A | 1 | a0001c0002t0030 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*630G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 630 | chr7 | 896052 | |||||
chr7:896072
|
C | T | 2 | a0001c0001t0005a0001c0002t0005 | 5 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*650C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 650 | chr7 | 896072 | |||||
chr7:896125
|
T | C | 1 | a0001c0001t0017 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 703 | chr7 | 896125 | |||||
chr7:896146
|
A | G | 1 | a0001c0005t0011 | 2 | HG02258.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*724A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 724 | chr7 | 896146 | |||||
chr7:896147
|
A | G | 2 | a0001c0001t0010a0001c0003t0010 | 2 | HG02647.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*725A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 725 | chr7 | 896147 | |||||
chr7:896168
|
T | C | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(25): Show | 235 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*746T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 746 | chr7 | 896168 | |||||
chr7:896169
|
G | A | 1 | a0001c0001t0012 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*747G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 747 | chr7 | 896169 | |||||
chr7:896182
|
G | A | 1 | a0001c0001t0031 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 760 | chr7 | 896182 | |||||
chr7:896270
|
G | A | 2 | a0001c0002t0006a0001c0003t0006 | 3 | HG01496.hp1 HG02647.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*848G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 848 | chr7 | 896270 | |||||
chr7:896270
|
G | C | 1 | a0001c0013t0032 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 848 | chr7 | 896270 | |||||
chr7:896273
|
G | T | 1 | a0001c0001t0029 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*851G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 851 | chr7 | 896273 | |||||
chr7:896293
|
A | G | 1 | a0001c0001t0009 | 2 | HG02071.hp1 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*871A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 871 | chr7 | 896293 | |||||
chr7:896312
|
A | G | 4 | a0001c0001t0033a0001c0010t0025a0001c0010t0026others(1): Show | 4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*890A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 890 | chr7 | 896312 | |||||
chr7:896354
|
C | T | 1 | a0001c0001t0008 | 2 | HG01192.hp1 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*932C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 932 | chr7 | 896354 | |||||
chr7:896405
|
C | T | 1 | a0001c0002t0019 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*983C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 983 | chr7 | 896405 | |||||
chr7:896430
|
A | G | 2 | a0001c0002t0006a0001c0003t0006 | 3 | HG01496.hp1 HG02647.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1008A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1008 | chr7 | 896430 | |||||
chr7:896433
|
G | A | 1 | a0001c0001t0018 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1011G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1011 | chr7 | 896433 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:876841
|
C | CCGCCGCC others(12): Show |
1 | a0001c0002t0002g0043 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.155+51_155+69dupCC others(17): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 876841 | |||||
chr7:876847
|
C | T | 1 | a0001c0002t0001g0295 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.155+47C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 876847 | ||||||
chr7:876897
|
C | G | 32 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0281others(29): Show | 34 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.155+97C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 876897 | ||||||
chr7:876978
|
C | A | 1 | a0001c0001t0002g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.155+178C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 876978 | ||||||
chr7:877041
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(280): Show | 346 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.155+241T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877041 | ||||||
chr7:877044
|
T | C | 3 | a0001c0001t0002g0047a0001c0003t0002g0046a0001c0011t0002g0045 | 3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+244T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877044 | ||||||
chr7:877045
|
G | T | 3 | a0001c0001t0002g0047a0001c0003t0002g0046a0001c0011t0002g0045 | 3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+245G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877045 | ||||||
chr7:877046
|
CG | C | 3 | a0001c0001t0002g0047a0001c0003t0002g0046a0001c0011t0002g0045 | 3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+247delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877046 | ||||||
chr7:877048
|
T | C | 3 | a0001c0001t0002g0047a0001c0003t0002g0046a0001c0011t0002g0045 | 3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+248T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877048 | ||||||
chr7:877049
|
T | C | 3 | a0001c0001t0002g0047a0001c0003t0002g0046a0001c0011t0002g0045 | 3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+249T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877049 | ||||||
chr7:877054
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0264 | 5 | HG01255.hp1 HG01256.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.155+254C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877054 | ||||||
chr7:877071
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.155+271C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877071 | ||||||
chr7:877105
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | NA19009.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.155+305A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877105 | ||||||
chr7:877151
|
C | T | 1 | a0001c0003t0006g0038 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.155+351C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877151 | ||||||
chr7:877179
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(113): Show | 163 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.155+379C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877179 | ||||||
chr7:877202
|
GCT | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(277): Show | 342 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.155+421_155+422del others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 877202 | |||||
chr7:877205
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.155+405C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877205 | ||||||
chr7:877225
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(81): Show | 110 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.155+425C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877225 | ||||||
chr7:877271
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(97): Show | 141 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.155+471C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877271 | ||||||
chr7:877300
|
GC | G | 12 | a0001c0001t0002g0258a0001c0001t0002g0261a0001c0001t0004g0253others(9): Show | 13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.155+506delC | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 877300 | |||||
chr7:877301
|
C | T | 1 | a0001c0002t0002g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.155+501C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877301 | ||||||
chr7:877404
|
G | A | 1 | a0001c0001t0004g0028 | 2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.155+604G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877404 | ||||||
chr7:877472
|
C | T | 1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155+672C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877472 | ||||||
chr7:877498
|
A | T | 2 | a0001c0001t0002g0033a0002c0007t0001g0015 | 5 | NA18954.hp1 NA18971.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.155+698A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877498 | ||||||
chr7:877547
|
C | T | 58 | a0001c0001t0033g0091a0001c0002t0001g0025a0001c0002t0001g0026others(55): Show | 64 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.155+747C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877547 | ||||||
chr7:877589
|
G | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(114): Show | 164 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.155+789G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877589 | ||||||
chr7:877591
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(114): Show | 164 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.155+791C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877591 | ||||||
chr7:877657
|
C | T | 11 | a0001c0002t0001g0027a0001c0002t0001g0130a0001c0002t0001g0132others(8): Show | 11 | HG02056.hp2 HG02074.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.155+857C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877657 | ||||||
chr7:877694
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.155+894G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877694 | ||||||
chr7:877697
|
C | G | 1 | a0001c0001t0001g0237 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.155+897C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877697 | ||||||
chr7:877715
|
C | A | 60 | a0001c0001t0033g0091a0001c0002t0001g0025a0001c0002t0001g0026others(57): Show | 66 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.155+915C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877715 | ||||||
chr7:877761
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(104): Show | 153 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.155+961C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877761 | ||||||
chr7:877826
|
C | G | 1 | a0001c0001t0001g0048 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.155+1026C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877826 | ||||||
chr7:877849
|
C | G | 1 | a0001c0002t0001g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.155+1049C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877849 | ||||||
chr7:877894
|
C | T | 1 | a0001c0003t0002g0294 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.155+1094C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877894 | ||||||
chr7:877916
|
C | T | 32 | a0001c0001t0001g0278a0001c0001t0001g0280a0001c0001t0001g0281others(29): Show | 34 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.155+1116C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877916 | ||||||
chr7:878002
|
C | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 7 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+1202C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878002 | ||||||
chr7:878037
|
T | A | 1 | a0001c0001t0004g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.155+1237T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878037 | ||||||
chr7:878096
|
C | T | 1 | a0001c0002t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.155+1296C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878096 | ||||||
chr7:878169
|
G | C | 1 | a0001c0001t0033g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155+1369G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878169 | ||||||
chr7:878191
|
G | A | 51 | a0001c0001t0033g0091a0001c0002t0001g0025a0001c0002t0001g0027others(48): Show | 56 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.155+1391G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878191 | ||||||
chr7:878210
|
G | A | 2 | a0001c0002t0005g0023a0001c0002t0005g0024 | 4 | HG00323.hp1 HG00642.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.155+1410G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878210 | ||||||
chr7:878214
|
C | G | 1 | a0001c0001t0002g0022 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.155+1414C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878214 | ||||||
chr7:878574
|
C | CT | 94 | a0001c0001t0001g0090a0001c0001t0001g0139a0001c0001t0001g0197others(91): Show | 100 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.155+1791dupT | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 878574 | |||||
chr7:878574
|
C | CTT | 8 | a0001c0001t0001g0293a0001c0002t0001g0025a0001c0002t0001g0157others(5): Show | 8 | HG03139.hp2 NA18953.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.155+1790_155+1791d others(4): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 878574 | |||||
chr7:878612
|
C | T | 1 | a0001c0002t0035g0117 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.155+1812C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878612 | ||||||
chr7:878615
|
C | T | 29 | a0001c0001t0001g0139a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+1815C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878615 | ||||||
chr7:878659
|
A | G | 1 | a0001c0002t0035g0117 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.155+1859A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878659 | ||||||
chr7:878747
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.155+1947A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878747 | ||||||
chr7:878773
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058 | 3 | HG02572.hp1 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.155+1973G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878773 | ||||||
chr7:878867
|
C | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(111): Show | 161 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.155+2067C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878867 | ||||||
chr7:878895
|
TA | T | 3 | a0001c0010t0025g0053a0001c0010t0026g0052a0001c0010t0028g0051 | 3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.155+2096delA | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878895 | ||||||
chr7:878976
|
A | AC | 71 | a0001c0001t0001g0293a0001c0001t0033g0091a0001c0002t0001g0025others(68): Show | 78 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.155+2185dupC | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 878976 | |||||
chr7:878976
|
AC | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(140): Show | 190 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.155+2185delC | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 878976 | |||||
chr7:878983
|
C | CG | 7 | a0001c0003t0002g0284a0001c0003t0002g0285a0001c0003t0002g0286others(4): Show | 7 | HG01261.hp1 HG01928.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+2183_155+2184i others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878983 | ||||||
chr7:879036
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.155+2236G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879036 | ||||||
chr7:879045
|
G | A | 1 | a0001c0001t0003g0059 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.155+2245G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879045 | ||||||
chr7:879108
|
C | G | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.155+2308C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879108 | ||||||
chr7:879126
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.155+2326T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879126 | ||||||
chr7:879177
|
T | G | 1 | a0001c0017t0002g0049 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155+2377T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879177 | ||||||
chr7:879242
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0002g0208 | 2 | HG01975.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.155+2442G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879242 | ||||||
chr7:879317
|
C | T | 2 | a0001c0001t0002g0196a0001c0001t0002g0201 | 2 | NA19063.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.155+2517C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879317 | ||||||
chr7:879360
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.155+2560T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879360 | ||||||
chr7:879391
|
A | G | 1 | a0001c0002t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.155+2591A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879391 | ||||||
chr7:879426
|
C | G | 1 | a0001c0002t0005g0024 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.155+2626C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879426 | ||||||
chr7:879496
|
C | T | 3 | a0001c0010t0025g0053a0001c0010t0026g0052a0001c0010t0028g0051 | 3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.155+2696C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879496 | ||||||
chr7:879543
|
G | A | 1 | a0001c0002t0015g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.155+2743G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879543 | ||||||
chr7:879725
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0163 | 3 | HG00735.hp2 HG01071.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.155+2925G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879725 | ||||||
chr7:879797
|
C | T | 4 | a0001c0002t0002g0011a0001c0002t0002g0112a0001c0002t0002g0113others(1): Show | 6 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+2997C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879797 | ||||||
chr7:879871
|
G | A | 1 | a0001c0001t0018g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.155+3071G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879871 | ||||||
chr7:880012
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.155+3212C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880012 | ||||||
chr7:880095
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.155+3295A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880095 | ||||||
chr7:880198
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.155+3398G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880198 | ||||||
chr7:880324
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.155+3524A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880324 | ||||||
chr7:880362
|
C | T | 1 | a0001c0003t0002g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.155+3562C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880362 | ||||||
chr7:880390
|
C | T | 1 | a0001c0003t0010g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.155+3590C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880390 | ||||||
chr7:880393
|
C | T | 29 | a0001c0001t0001g0139a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+3593C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880393 | ||||||
chr7:880432
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.155+3632C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880432 | ||||||
chr7:880458
|
G | A | 7 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122others(4): Show | 8 | HG02615.hp1 HG02615.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.155+3658G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880458 | ||||||
chr7:880575
|
G | A | 3 | a0001c0001t0001g0243a0001c0003t0002g0244a0001c0003t0002g0252 | 3 | HG02602.hp2 HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.155+3775G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880575 | ||||||
chr7:880609
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.155+3809G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880609 | ||||||
chr7:880617
|
A | C | 1 | a0001c0003t0002g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.155+3817A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880617 | ||||||
chr7:880664
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(112): Show | 162 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.155+3864C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880664 | ||||||
chr7:880665
|
G | A | 1 | a0001c0002t0002g0136 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.155+3865G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880665 | ||||||
chr7:880746
|
G | A | 4 | a0001c0002t0001g0115a0001c0002t0003g0094a0001c0002t0003g0095others(1): Show | 4 | NA18946.hp2 NA18950.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.155+3946G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880746 | ||||||
chr7:880775
|
C | G | 29 | a0001c0001t0001g0139a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+3975C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880775 | ||||||
chr7:880781
|
A | G | 29 | a0001c0001t0001g0139a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+3981A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880781 | ||||||
chr7:880840
|
C | T | 50 | a0001c0002t0001g0025a0001c0002t0001g0027a0001c0002t0001g0093others(47): Show | 55 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.155+4040C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880840 | ||||||
chr7:880876
|
G | A | 1 | a0001c0017t0002g0049 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155+4076G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880876 | ||||||
chr7:880911
|
C | T | 29 | a0001c0001t0001g0139a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+4111C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880911 | ||||||
chr7:881054
|
G | A | 1 | a0001c0003t0006g0038 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.155+4254G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881054 | ||||||
chr7:881131
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155+4331C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881131 | ||||||
chr7:881205
|
G | A | 1 | a0001c0001t0002g0173 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.155+4405G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881205 | ||||||
chr7:881362
|
C | T | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.155+4562C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881362 | ||||||
chr7:881363
|
G | A | 2 | a0001c0003t0002g0169a0001c0003t0010g0168 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.155+4563G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881363 | ||||||
chr7:881438
|
C | T | 1 | a0001c0001t0002g0201 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.156-4618C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881438 | ||||||
chr7:881688
|
G | A | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.156-4368G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881688 | ||||||
chr7:881707
|
C | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(100): Show | 148 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.156-4349C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881707 | ||||||
chr7:881754
|
C | G | 32 | a0001c0001t0001g0139a0001c0001t0014g0054a0001c0001t0014g0055others(29): Show | 32 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.156-4302C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881754 | ||||||
chr7:881771
|
A | G | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.156-4285A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881771 | ||||||
chr7:881774
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(55): Show | 84 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.156-4282G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881774 | ||||||
chr7:881798
|
A | G | 1 | a0001c0002t0003g0111 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.156-4258A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881798 | ||||||
chr7:881990
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.156-4066T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881990 | ||||||
chr7:882007
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(280): Show | 346 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.156-4049T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882007 | ||||||
chr7:882030
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.156-4026T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882030 | ||||||
chr7:882035
|
C | T | 4 | a0001c0001t0004g0028a0001c0001t0004g0164a0001c0001t0004g0165others(1): Show | 5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-4021C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882035 | ||||||
chr7:882154
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.156-3902T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882154 | ||||||
chr7:882219
|
T | C | 1 | a0001c0002t0020g0098 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.156-3837T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882219 | ||||||
chr7:882253
|
C | G | 1 | a0001c0001t0013g0194 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.156-3803C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882253 | ||||||
chr7:882355
|
G | A | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.156-3701G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882355 | ||||||
chr7:882460
|
C | T | 3 | a0001c0005t0011g0277a0001c0005t0011g0291a0001c0006t0002g0276 | 3 | HG02258.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.156-3596C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882460 | ||||||
chr7:882577
|
A | AGGGATGG others(30): Show |
5 | a0001c0001t0009g0178a0001c0010t0025g0053a0001c0010t0026g0052others(2): Show | 5 | HG02071.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-3385_156-3349d others(39): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 882577 | |||||
chr7:882577
|
A | G | 45 | a0001c0001t0001g0139a0001c0001t0014g0054a0001c0001t0014g0055others(42): Show | 45 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.156-3479A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882577 | ||||||
chr7:882577
|
AGGGATGG others(30): Show |
A | 13 | a0001c0001t0002g0047a0001c0001t0002g0258a0001c0001t0002g0261others(10): Show | 14 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.156-3385_156-3349d others(39): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 882577 | |||||
chr7:882582
|
T | A | 4 | a0001c0002t0003g0128a0001c0002t0003g0129a0001c0002t0021g0127others(1): Show | 4 | HG02148.hp2 NA19011.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-3474T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882582 | ||||||
chr7:882622
|
C | T | 2 | a0001c0003t0001g0170a0001c0003t0002g0046 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.156-3434C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882622 | ||||||
chr7:882651
|
G | A | 3 | a0001c0002t0002g0137a0001c0002t0002g0138a0001c0002t0002g0158 | 3 | NA18979.hp2 NA19055.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.156-3405G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882651 | ||||||
chr7:882699
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 7 | NA18943.hp2 NA18944.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.156-3357G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882699 | ||||||
chr7:882825
|
G | C | 1 | a0001c0010t0028g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.156-3231G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882825 | ||||||
chr7:882840
|
C | G | 29 | a0001c0002t0001g0088a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.156-3216C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882840 | ||||||
chr7:882874
|
A | G | 32 | a0001c0001t0001g0139a0001c0001t0014g0054a0001c0001t0014g0055others(29): Show | 32 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.156-3182A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882874 | ||||||
chr7:882876
|
A | C | 1 | a0001c0005t0011g0277 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.156-3180A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882876 | ||||||
chr7:882905
|
G | C | 2 | a0001c0001t0001g0200a0001c0001t0002g0199 | 2 | HG01167.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.156-3151G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882905 | ||||||
chr7:882910
|
CCT | C | 17 | a0001c0003t0002g0041a0001c0003t0002g0269a0001c0003t0002g0270others(14): Show | 19 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.156-3145_156-3144d others(4): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882910 | ||||||
chr7:882921
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 359 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.156-3135A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882921 | ||||||
chr7:883194
|
G | T | 3 | a0001c0005t0011g0277a0001c0005t0011g0291a0001c0006t0002g0276 | 3 | HG02258.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.156-2862G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883194 | ||||||
chr7:883222
|
C | G | 29 | a0001c0002t0001g0088a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.156-2834C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883222 | ||||||
chr7:883240
|
G | A | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0230others(2): Show | 5 | HG02080.hp2 NA18992.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-2816G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883240 | ||||||
chr7:883444
|
A | G | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.156-2612A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883444 | ||||||
chr7:883563
|
A | G | 1 | a0001c0001t0002g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.156-2493A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883563 | ||||||
chr7:883643
|
T | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0139a0001c0001t0001g0209others(33): Show | 39 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.156-2413T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883643 | ||||||
chr7:883930
|
C | T | 4 | a0001c0006t0002g0267a0001c0006t0002g0289a0001c0006t0002g0290others(1): Show | 4 | HG01081.hp2 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-2126C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883930 | ||||||
chr7:883981
|
G | A | 4 | a0001c0001t0004g0028a0001c0001t0004g0164a0001c0001t0004g0165others(1): Show | 5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-2075G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883981 | ||||||
chr7:884020
|
C | T | 1 | a0001c0006t0002g0267 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.156-2036C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884020 | ||||||
chr7:884025
|
G | A | 11 | a0001c0001t0002g0258a0001c0001t0002g0261a0001c0001t0004g0253others(8): Show | 12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.156-2031G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884025 | ||||||
chr7:884123
|
C | T | 1 | a0001c0001t0033g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.156-1933C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884123 | ||||||
chr7:884162
|
G | A | 7 | a0001c0005t0011g0277a0001c0005t0011g0291a0001c0006t0002g0267others(4): Show | 7 | HG01081.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.156-1894G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884162 | ||||||
chr7:884218
|
G | A | 31 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0002t0001g0088others(28): Show | 31 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.156-1838G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884218 | ||||||
chr7:884233
|
G | A | 1 | a0001c0010t0028g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.156-1823G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884233 | ||||||
chr7:884298
|
G | A | 29 | a0001c0002t0001g0088a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.156-1758G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884298 | ||||||
chr7:884343
|
C | T | 2 | a0001c0003t0001g0170a0001c0003t0002g0046 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.156-1713C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884343 | ||||||
chr7:884424
|
C | T | 29 | a0001c0002t0001g0088a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.156-1632C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884424 | ||||||
chr7:884479
|
C | T | 1 | a0001c0001t0018g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.156-1577C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884479 | ||||||
chr7:884495
|
C | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(58): Show | 70 | HG00558.hp2 HG00639.hp2 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.156-1561C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884495 | ||||||
chr7:884508
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.156-1548T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884508 | ||||||
chr7:884512
|
C | G | 1 | a0001c0003t0010g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.156-1544C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884512 | ||||||
chr7:884547
|
G | A | 1 | a0001c0001t0001g0039 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.156-1509G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884547 | ||||||
chr7:884557
|
G | T | 30 | a0001c0001t0002g0193a0001c0002t0001g0088a0001c0002t0001g0141others(27): Show | 30 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.156-1499G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884557 | ||||||
chr7:884593
|
C | T | 1 | a0001c0014t0001g0283 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.156-1463C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884593 | ||||||
chr7:884625
|
C | T | 1 | a0001c0003t0002g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.156-1431C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884625 | ||||||
chr7:884709
|
G | A | 1 | a0001c0003t0002g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.156-1347G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884709 | ||||||
chr7:884791
|
T | C | 1 | a0001c0002t0002g0140 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.156-1265T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884791 | ||||||
chr7:884800
|
T | A | 1 | a0001c0002t0019g0107 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.156-1256T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884800 | ||||||
chr7:884813
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.156-1243C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884813 | ||||||
chr7:884979
|
A | G | 12 | a0001c0001t0002g0258a0001c0001t0002g0261a0001c0001t0004g0253others(9): Show | 13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.156-1077A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884979 | ||||||
chr7:885133
|
A | T | 1 | a0001c0002t0002g0158 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.156-923A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885133 | ||||||
chr7:885154
|
G | T | 1 | a0001c0003t0034g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.156-902G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885154 | ||||||
chr7:885166
|
C | G | 4 | a0001c0001t0002g0036a0001c0002t0001g0026a0001c0002t0001g0120others(1): Show | 6 | HG02615.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.156-890C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885166 | ||||||
chr7:885257
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.156-799C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885257 | ||||||
chr7:885278
|
C | T | 1 | a0002c0007t0001g0015 | 3 | NA18954.hp1 NA19067.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.156-778C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885278 | ||||||
chr7:885347
|
C | T | 2 | a0001c0002t0005g0023a0001c0002t0005g0024 | 4 | HG00323.hp1 HG00642.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-709C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885347 | ||||||
chr7:885382
|
A | G | 9 | a0001c0001t0001g0293a0001c0005t0011g0277a0001c0005t0011g0291others(6): Show | 9 | HG01081.hp2 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.156-674A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885382 | ||||||
chr7:885395
|
C | T | 54 | a0001c0001t0001g0245a0001c0002t0001g0025a0001c0002t0001g0027others(51): Show | 59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.156-661C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885395 | ||||||
chr7:885417
|
C | T | 8 | a0001c0001t0002g0002a0001c0001t0002g0173a0001c0001t0002g0196others(5): Show | 14 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.156-639C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885417 | ||||||
chr7:885421
|
A | AC | 11 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0174others(8): Show | 11 | HG01243.hp1 HG01978.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.156-631dupC | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 885421 | |||||
chr7:885425
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0282 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.156-631C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885425 | ||||||
chr7:885426
|
G | A | 1 | a0001c0001t0037g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.156-630G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885426 | ||||||
chr7:885434
|
G | T | 4 | a0001c0001t0004g0028a0001c0001t0004g0164a0001c0001t0004g0165others(1): Show | 5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-622G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885434 | ||||||
chr7:885507
|
G | A | 1 | a0001c0004t0004g0254 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.156-549G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885507 | ||||||
chr7:885548
|
G | A | 1 | a0001c0001t0002g0022 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.156-508G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885548 | ||||||
chr7:885717
|
C | G | 60 | a0001c0001t0001g0245a0001c0001t0033g0091a0001c0002t0001g0025others(57): Show | 66 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.156-339C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885717 | ||||||
chr7:885911
|
G | A | 1 | a0001c0003t0002g0041 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.156-145G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885911 | ||||||
chr7:885997
|
C | CG | 6 | a0001c0001t0001g0087a0001c0001t0002g0047a0001c0002t0002g0114others(3): Show | 6 | HG01175.hp1 HG01928.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-54dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 885997 | |||||
chr7:886007
|
C | CG | 8 | a0001c0001t0001g0057a0001c0001t0002g0198a0001c0001t0002g0199others(5): Show | 8 | HG00544.hp1 HG00735.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.156-47dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 886007 | |||||
chr7:886011
|
G | C | 9 | a0001c0001t0001g0293a0001c0005t0011g0277a0001c0005t0011g0291others(6): Show | 9 | HG01081.hp2 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.156-45G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 886011 | ||||||
chr7:886049
|
G | C | 1 | a0001c0010t0028g0051 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.156-7G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 886049 | ||||||
chr7:886135
|
GTAAGCCG others(54): Show |
G | 1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.234+3_234+63delAAG others(58): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 886135 | |||||
chr7:886159
|
A | G | 30 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0002t0001g0088others(27): Show | 30 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.234+25A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886159 | ||||||
chr7:886229
|
C | T | 55 | a0001c0001t0001g0245a0001c0002t0001g0025a0001c0002t0001g0027others(52): Show | 60 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.234+95C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886229 | ||||||
chr7:886312
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(172): Show | 224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.234+178A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886312 | ||||||
chr7:886330
|
G | A | 19 | a0001c0003t0002g0041a0001c0003t0002g0244a0001c0003t0002g0252others(16): Show | 21 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+196G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886330 | ||||||
chr7:886355
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0002g0199 | 2 | HG01167.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.235-214G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886355 | ||||||
chr7:886424
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0002g0199 | 2 | HG01167.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.235-145G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886424 | ||||||
chr7:886440
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(140): Show | 192 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.235-129G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886440 | ||||||
chr7:886468
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0172a0001c0001t0001g0174others(3): Show | 8 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.235-101C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886468 | ||||||
chr7:886472
|
C | T | 2 | a0001c0002t0002g0092a0001c0002t0002g0106 | 2 | HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.235-97C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886472 | ||||||
chr7:886503
|
T | C | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.235-66T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886503 | ||||||
chr7:886669
|
ACCCCGGG others(30): Show |
A | 1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.316+27_316+63delAC others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 886669 | |||||
chr7:886731
|
G | A | 2 | a0001c0002t0002g0092a0001c0002t0002g0106 | 2 | HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.316+81G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 886731 | ||||||
chr7:886785
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.316+135G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 886785 | ||||||
chr7:886838
|
C | G | 1 | a0001c0003t0002g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.316+188C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 886838 | ||||||
chr7:887026
|
A | G | 31 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0002t0001g0088others(28): Show | 31 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.317-344A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887026 | ||||||
chr7:887042
|
C | T | 1 | a0001c0002t0002g0156 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.317-328C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887042 | ||||||
chr7:887154
|
G | GCGTC | 29 | a0001c0002t0001g0088a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.317-210_317-207dup others(4): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 887154 | |||||
chr7:887220
|
G | A | 4 | a0001c0001t0004g0028a0001c0001t0004g0164a0001c0001t0004g0165others(1): Show | 5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-150G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887220 | ||||||
chr7:887333
|
C | G | 1 | a0001c0001t0001g0009 | 4 | HG00323.hp2 HG00642.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-37C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887333 | ||||||
chr7:887334
|
G | A | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.317-36G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887334 | ||||||
chr7:887640
|
C | T | 1 | a0001c0001t0001g0008 | 4 | HG02886.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+121C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887640 | ||||||
chr7:887643
|
G | A | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.466+124G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887643 | ||||||
chr7:887661
|
C | G | 29 | a0001c0002t0001g0088a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.466+142C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887661 | ||||||
chr7:887681
|
G | A | 1 | a0001c0002t0002g0142 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.466+162G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887681 | ||||||
chr7:887727
|
C | T | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.466+208C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887727 | ||||||
chr7:887731
|
C | T | 1 | a0001c0001t0029g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.466+212C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887731 | ||||||
chr7:887734
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.466+215C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887734 | ||||||
chr7:887791
|
G | C | 11 | a0001c0001t0002g0258a0001c0001t0002g0261a0001c0001t0004g0253others(8): Show | 12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.466+272G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887791 | ||||||
chr7:887801
|
C | T | 12 | a0001c0001t0002g0258a0001c0001t0002g0261a0001c0001t0004g0253others(9): Show | 13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.466+282C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887801 | ||||||
chr7:887831
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 6 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+312T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887831 | ||||||
chr7:887836
|
C | T | 3 | a0001c0010t0025g0053a0001c0010t0026g0052a0001c0010t0028g0051 | 3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.466+317C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887836 | ||||||
chr7:887901
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0264a0001c0020t0001g0119 | 6 | HG01106.hp2 HG01255.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+382G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887901 | ||||||
chr7:888010
|
ATTGAGTG others(33): Show |
A | 1 | a0001c0009t0001g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.466+492_466+531del others(40): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888010 | ||||||
chr7:888026
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.466+507G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888026 | ||||||
chr7:888058
|
C | T | 1 | a0001c0001t0003g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.466+539C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888058 | ||||||
chr7:888125
|
G | A | 21 | a0001c0003t0002g0041a0001c0003t0002g0169a0001c0003t0002g0244others(18): Show | 23 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.466+606G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888125 | ||||||
chr7:888150
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.466+631T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888150 | ||||||
chr7:888290
|
T | C | 33 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0002t0001g0088others(30): Show | 34 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.466+771T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888290 | ||||||
chr7:888446
|
C | A | 1 | a0001c0003t0002g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466+927C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888446 | ||||||
chr7:888485
|
T | C | 1 | a0001c0019t0001g0126 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.466+966T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888485 | ||||||
chr7:888553
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.466+1034G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888553 | ||||||
chr7:888583
|
C | T | 4 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0003t0006g0038others(1): Show | 5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+1064C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888583 | ||||||
chr7:888710
|
C | G | 3 | a0001c0010t0025g0053a0001c0010t0026g0052a0001c0010t0028g0051 | 3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.466+1191C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888710 | ||||||
chr7:888740
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 333 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(330): Show |
intron_variant | MODIFIER | c.466+1221T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888740 | ||||||
chr7:888743
|
G | A | 1 | a0001c0003t0002g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466+1224G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888743 | ||||||
chr7:888781
|
G | A | 1 | a0001c0001t0008g0182 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.466+1262G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888781 | ||||||
chr7:888887
|
G | A | 4 | a0001c0002t0001g0108a0001c0002t0001g0109a0001c0002t0003g0111others(1): Show | 4 | HG02040.hp2 HG02135.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+1368G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888887 | ||||||
chr7:888967
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.466+1448G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888967 | ||||||
chr7:888999
|
C | T | 55 | a0001c0001t0001g0245a0001c0002t0001g0025a0001c0002t0001g0027others(52): Show | 60 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.466+1480C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888999 | ||||||
chr7:889026
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.466+1507T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889026 | ||||||
chr7:889053
|
T | C | 3 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122 | 4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+1534T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889053 | ||||||
chr7:889074
|
T | C | 1 | a0001c0002t0002g0159 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.466+1555T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889074 | ||||||
chr7:889089
|
G | A | 2 | a0001c0002t0006g0050a0001c0017t0002g0049 | 2 | HG01496.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.466+1570G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889089 | ||||||
chr7:889244
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(128): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.467-1684C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889244 | ||||||
chr7:889268
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.467-1660C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889268 | ||||||
chr7:889275
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.467-1653G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889275 | ||||||
chr7:889282
|
C | G | 1 | a0001c0001t0002g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.467-1646C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889282 | ||||||
chr7:889301
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.467-1627A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889301 | ||||||
chr7:889421
|
C | T | 3 | a0001c0010t0025g0053a0001c0010t0026g0052a0001c0010t0028g0051 | 3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.467-1507C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889421 | ||||||
chr7:889486
|
C | T | 60 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(57): Show | 66 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.467-1442C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889486 | ||||||
chr7:889503
|
A | G | 3 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0003t0006g0038 | 4 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1425A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889503 | ||||||
chr7:889574
|
C | T | 4 | a0001c0003t0002g0046a0001c0010t0025g0053a0001c0010t0026g0052others(1): Show | 4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1354C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889574 | ||||||
chr7:889666
|
TAGGACGG others(260): Show |
T | 1 | a0001c0001t0014g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.467-1246_467-980de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889666 | |||||
chr7:889666
|
TAGGACGG others(300): Show |
T | 3 | a0001c0001t0014g0055a0001c0003t0006g0038a0001c0011t0002g0045 | 4 | HG02647.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-1246_467-940de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889666 | |||||
chr7:889699
|
C | CG | 3 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0229 | 5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1226dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889699 | |||||
chr7:889703
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0229 | 5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1225C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889703 | ||||||
chr7:889708
|
GAGCGGAG others(205): Show |
G | 3 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0229 | 5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1219_467-1008d others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889708 | ||||||
chr7:889720
|
T | C | 4 | a0001c0004t0002g0256a0001c0005t0011g0277a0001c0005t0011g0291others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1208T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889720 | ||||||
chr7:889720
|
T | TGCGAGCG others(608): Show |
1 | a0001c0001t0001g0066 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.467-1199_467-1198i others(617): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889720 | |||||
chr7:889726
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.467-1202C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889726 | ||||||
chr7:889733
|
T | C | 2 | a0001c0001t0001g0066a0001c0004t0002g0256 | 2 | NA18983.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.467-1195T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889733 | ||||||
chr7:889742
|
G | C | 1 | a0001c0005t0040g0265 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.467-1186G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889742 | ||||||
chr7:889743
|
T | C | 3 | a0001c0001t0001g0089a0001c0002t0002g0092a0001c0002t0002g0106 | 3 | HG02896.hp1 HG03579.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.467-1185T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889743 | ||||||
chr7:889743
|
T | TCTGGGAG others(33): Show |
4 | a0001c0002t0002g0155a0001c0002t0006g0050a0001c0015t0002g0096others(1): Show | 4 | HG01496.hp1 HG02148.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1166_467-1165i others(42): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889743 | |||||
chr7:889743
|
T | TCTGGGAG others(73): Show |
14 | a0001c0002t0001g0141a0001c0002t0001g0148a0001c0002t0002g0136others(11): Show | 14 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.467-1166_467-1165i others(82): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889743 | |||||
chr7:889762
|
C | A | 45 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(42): Show | 52 | HG00558.hp2 HG02027.hp2 HG02071.hp2 others(49): Show |
intron_variant | MODIFIER | c.467-1166C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889762 | ||||||
chr7:889763
|
G | A | 84 | a0001c0001t0001g0081a0001c0001t0002g0022a0001c0001t0002g0044others(81): Show | 92 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.467-1165G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889763 | ||||||
chr7:889773
|
T | C | 8 | a0001c0001t0001g0066a0001c0001t0001g0278a0001c0001t0001g0282others(5): Show | 8 | HG01081.hp1 HG01261.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-1155T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889773 | ||||||
chr7:889773
|
T | TAGGACGG others(33): Show |
4 | a0001c0003t0002g0041a0001c0003t0002g0270a0001c0005t0001g0275others(1): Show | 5 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-1127_467-1126i others(42): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889773 | |||||
chr7:889773
|
TAGGACGG others(153): Show |
T | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(97): Show | 140 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.467-1145_467-986de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889773 | |||||
chr7:889773
|
TAGGACGG others(193): Show |
T | 1 | a0001c0001t0001g0030 | 2 | HG01261.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.467-1145_467-946de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889773 | |||||
chr7:889783
|
C | CCTGGGAG others(633): Show |
1 | a0001c0003t0010g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.467-1127_467-1126i others(642): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889783 | |||||
chr7:889783
|
C | CCTGGGAG others(433): Show |
1 | a0001c0003t0002g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.467-1127_467-1126i others(442): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889783 | |||||
chr7:889783
|
C | T | 30 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0171others(27): Show | 33 | HG00544.hp1 HG00733.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.467-1145C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889783 | ||||||
chr7:889794
|
A | AGGGAGCG others(233): Show |
1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.467-1127_467-1126i others(242): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889794 | |||||
chr7:889802
|
A | AGAGCGGG others(513): Show |
1 | a0001c0001t0001g0056 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.467-1106_467-1105i others(522): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889802 | |||||
chr7:889802
|
A | AGAGCGGG others(513): Show |
1 | a0001c0001t0001g0058 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.467-1106_467-1105i others(522): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889802 | |||||
chr7:889802
|
A | AGAGCGGG others(72): Show |
13 | a0001c0002t0001g0141a0001c0002t0001g0148a0001c0002t0002g0136others(10): Show | 13 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-1067_467-1066i others(81): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889802 | |||||
chr7:889802
|
A | C | 111 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0171others(108): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.467-1126A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889802 | ||||||
chr7:889802
|
A | T | 3 | a0001c0005t0011g0277a0001c0005t0011g0291a0001c0006t0002g0276 | 3 | HG02258.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.467-1126A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889802 | ||||||
chr7:889806
|
C | T | 5 | a0001c0005t0040g0265a0001c0006t0002g0267a0001c0006t0002g0289others(2): Show | 5 | HG01081.hp2 HG01891.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1122C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889806 | ||||||
chr7:889813
|
T | C | 32 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0247others(29): Show | 34 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.467-1115T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889813 | ||||||
chr7:889813
|
T | TAGGACGG others(433): Show |
1 | a0001c0001t0001g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.467-1106_467-1105i others(442): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889813 | |||||
chr7:889813
|
T | TAGGACGG others(513): Show |
1 | a0001c0001t0001g0280 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.467-1076_467-1075i others(522): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889813 | |||||
chr7:889819
|
G | GGGGCCTG others(112): Show |
2 | a0001c0002t0002g0151a0001c0002t0002g0161 | 2 | NA18947.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.467-1106_467-1105i others(121): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889819 | |||||
chr7:889819
|
G | GGGGCCTG others(1267): Show |
1 | a0001c0002t0002g0146 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.467-1106_467-1105i others(1276): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889819 | |||||
chr7:889823
|
T | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(116): Show | 133 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.467-1105T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889823 | ||||||
chr7:889842
|
C | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(32): Show | 42 | HG00558.hp2 HG02027.hp2 HG02071.hp2 others(39): Show |
intron_variant | MODIFIER | c.467-1086C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889842 | ||||||
chr7:889846
|
C | T | 1 | a0001c0017t0002g0049 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-1082C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889846 | ||||||
chr7:889853
|
T | C | 45 | a0001c0001t0001g0020a0001c0001t0001g0057a0001c0001t0001g0062others(42): Show | 48 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.467-1075T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889853 | ||||||
chr7:889853
|
TAGGACGG others(113): Show |
T | 5 | a0001c0001t0001g0234a0001c0002t0002g0043a0001c0010t0025g0053others(2): Show | 5 | HG00733.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1006_467-887de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889853 | |||||
chr7:889858
|
CG | C | 4 | a0001c0002t0001g0115a0001c0002t0003g0094a0001c0002t0003g0095others(1): Show | 4 | NA18946.hp2 NA18950.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1066delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889858 | |||||
chr7:889859
|
G | C | 1 | a0001c0004t0002g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.467-1069G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889859 | ||||||
chr7:889859
|
G | GGGGTCTG others(1227): Show |
2 | a0001c0002t0002g0159a0001c0002t0002g0162 | 2 | HG00621.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.467-1047_467-1046i others(1236): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889859 | |||||
chr7:889882
|
C | A | 13 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122others(10): Show | 14 | HG02615.hp2 HG02895.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.467-1046C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889882 | ||||||
chr7:889882
|
C | CGAGCGGG others(112): Show |
1 | a0001c0002t0002g0155 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.467-1027_467-1026i others(121): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889882 | |||||
chr7:889882
|
C | T | 13 | a0001c0002t0001g0141a0001c0002t0001g0148a0001c0002t0002g0136others(10): Show | 13 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-1046C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889882 | ||||||
chr7:889893
|
T | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(78): Show | 92 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.467-1035T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889893 | ||||||
chr7:889893
|
T | TAGGACGG others(33): Show |
1 | a0001c0001t0001g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.467-1007_467-1006i others(42): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889893 | |||||
chr7:889893
|
T | TAGGACGG others(232): Show |
1 | a0001c0015t0002g0096 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.467-1027_467-1026i others(241): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889893 | |||||
chr7:889893
|
T | TAGGACGG others(303): Show |
1 | a0001c0019t0001g0126 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.467-1027_467-1026i others(312): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889893 | |||||
chr7:889898
|
CG | C | 5 | a0001c0001t0001g0177a0001c0001t0037g0213a0001c0002t0002g0092others(2): Show | 5 | HG01496.hp1 HG01891.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-1026delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889898 | |||||
chr7:889899
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.467-1029G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889899 | ||||||
chr7:889899
|
G | GGGTCTGG others(31): Show |
1 | a0001c0004t0002g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.467-1027_467-1026i others(40): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889899 | |||||
chr7:889903
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.467-1025T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889903 | ||||||
chr7:889903
|
T | TCTGGGAG others(509): Show |
2 | a0001c0005t0011g0277a0001c0006t0002g0276 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.467-1007_467-1006i others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889903 | |||||
chr7:889915
|
GGGAGCGA others(191): Show |
G | 1 | a0001c0001t0002g0196 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.467-1010_467-813de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889915 | |||||
chr7:889922
|
A | AGAGCGGG others(832): Show |
1 | a0001c0004t0004g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.467-996_467-995ins others(839): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889922 | |||||
chr7:889922
|
A | AGAGCGGG others(353): Show |
1 | a0001c0004t0004g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.467-996_467-995ins others(360): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889922 | |||||
chr7:889922
|
A | C | 143 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(140): Show | 163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.467-1006A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889922 | ||||||
chr7:889922
|
A | T | 24 | a0001c0001t0003g0059a0001c0002t0001g0115a0001c0002t0001g0141others(21): Show | 24 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.467-1006A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889922 | ||||||
chr7:889926
|
C | CGGGTGTT others(351): Show |
1 | a0001c0017t0002g0049 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-996_467-995ins others(358): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889926 | |||||
chr7:889926
|
C | CGGGTGTT others(351): Show |
1 | a0001c0002t0002g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.467-996_467-995ins others(358): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889926 | |||||
chr7:889926
|
C | T | 2 | a0001c0002t0002g0146a0001c0019t0001g0126 | 2 | HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.467-1002C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889926 | ||||||
chr7:889927
|
G | A | 1 | a0001c0019t0001g0126 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.467-1001G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889927 | ||||||
chr7:889933
|
C | T | 95 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0056others(92): Show | 106 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.467-995C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889933 | ||||||
chr7:889938
|
CG | C | 60 | a0001c0001t0001g0019a0001c0001t0001g0171a0001c0001t0001g0177others(57): Show | 68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.467-986delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889938 | |||||
chr7:889939
|
G | GGGTCTGG others(31): Show |
4 | a0001c0005t0040g0265a0001c0006t0002g0267a0001c0006t0002g0289others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-987_467-986ins others(38): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889939 | |||||
chr7:889943
|
T | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0229others(14): Show | 19 | HG00544.hp1 HG01106.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.467-985T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889943 | ||||||
chr7:889943
|
T | TCTGGGAG others(467): Show |
1 | a0001c0009t0001g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.467-927_467-926ins others(474): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889943 | |||||
chr7:889943
|
T | TCTGGGAG others(33): Show |
1 | a0001c0002t0007g0160 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.467-967_467-966ins others(40): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889943 | |||||
chr7:889951
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0229 | 5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-977T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889951 | ||||||
chr7:889960
|
C | CGCGAGCG others(313): Show |
1 | a0001c0001t0003g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(320): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889960 | |||||
chr7:889960
|
C | T | 1 | a0001c0002t0002g0118 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.467-968C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889960 | ||||||
chr7:889962
|
C | A | 6 | a0001c0001t0001g0264a0001c0001t0002g0258a0001c0001t0002g0261others(3): Show | 6 | HG00621.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-966C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889962 | ||||||
chr7:889962
|
C | T | 8 | a0001c0002t0002g0092a0001c0002t0002g0106a0001c0002t0002g0151others(5): Show | 8 | HG01175.hp1 HG01496.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-966C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889962 | ||||||
chr7:889962
|
CGAGCGGG others(430): Show |
C | 3 | a0001c0001t0001g0171a0001c0001t0001g0177a0001c0001t0037g0213 | 3 | HG01891.hp2 HG02976.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.467-955_467-519del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889962 | |||||
chr7:889963
|
G | A | 1 | a0001c0001t0014g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.467-965G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889963 | ||||||
chr7:889966
|
C | T | 3 | a0001c0001t0001g0226a0001c0002t0002g0159a0001c0002t0002g0162 | 3 | HG00621.hp2 HG03942.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.467-962C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889966 | ||||||
chr7:889970
|
T | G | 1 | a0001c0001t0001g0066 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.467-958T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889970 | ||||||
chr7:889973
|
C | CAGGACGG others(513): Show |
1 | a0001c0003t0002g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(520): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889973 | |||||
chr7:889973
|
C | CAGGACGG others(551): Show |
1 | a0001c0001t0027g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.467-927_467-926ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889973 | |||||
chr7:889973
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(191): Show | 245 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.467-955C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889973 | ||||||
chr7:889978
|
CG | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0056a0001c0001t0001g0058others(3): Show | 9 | HG01081.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-946delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889978 | |||||
chr7:889979
|
G | GGGGCCTG others(671): Show |
1 | a0001c0001t0036g0279 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(678): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGCCTG others(631): Show |
1 | a0001c0001t0001g0281 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGCCTG others(631): Show |
1 | a0001c0001t0001g0083 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGCCTG others(511): Show |
1 | a0001c0001t0003g0070 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGCCTG others(511): Show |
1 | a0001c0001t0003g0071 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(591): Show |
2 | a0001c0001t0001g0278a0001c0001t0001g0282 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.467-916_467-915ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(512): Show |
1 | a0001c0002t0001g0088 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.467-916_467-915ins others(519): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(551): Show |
5 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0003g0006others(2): Show | 8 | HG02071.hp2 HG02129.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(631): Show |
2 | a0001c0001t0001g0068a0001c0001t0001g0074 | 2 | NA18946.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.467-916_467-915ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(591): Show |
1 | a0001c0001t0001g0075 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.467-916_467-915ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(551): Show |
2 | a0001c0001t0001g0061a0001c0001t0003g0076 | 2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(551): Show |
2 | a0001c0001t0003g0077a0001c0001t0003g0238 | 2 | HG02027.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(631): Show |
5 | a0001c0001t0001g0048a0001c0001t0001g0084a0001c0001t0001g0085others(2): Show | 5 | NA18612.hp2 NA18984.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-916_467-915ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(591): Show |
2 | a0001c0001t0003g0059a0001c0001t0018g0060 | 2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.467-916_467-915ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(551): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0062 | 5 | NA18944.hp2 NA18967.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(551): Show |
8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0063others(5): Show | 9 | HG00558.hp2 HG02135.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(511): Show |
1 | a0001c0001t0001g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.467-916_467-915ins others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(550): Show |
1 | a0001c0004t0004g0254 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(557): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(591): Show |
1 | a0001c0001t0002g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.467-916_467-915ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(630): Show |
1 | a0001c0004t0002g0255 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(637): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(590): Show |
1 | a0001c0001t0002g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(597): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(550): Show |
2 | a0001c0001t0004g0253a0001c0004t0002g0040 | 3 | HG02257.hp2 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.467-916_467-915ins others(557): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(550): Show |
3 | a0001c0004t0002g0257a0001c0004t0002g0262a0001c0014t0001g0283 | 3 | HG02723.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.467-916_467-915ins others(557): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGGTCTG others(592): Show |
1 | a0001c0001t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.467-927_467-926ins others(599): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889979
|
G | GGGTCTGG others(150): Show |
2 | a0001c0005t0001g0275a0001c0008t0001g0271 | 2 | HG01175.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.467-947_467-946ins others(157): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | |||||
chr7:889980
|
G | GGGTCTGG others(116): Show |
1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.467-927_467-926ins others(123): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889980 | |||||
chr7:889983
|
T | C | 7 | a0001c0001t0014g0054a0001c0002t0001g0115a0001c0002t0002g0151others(4): Show | 7 | HG01243.hp2 NA18946.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-945T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889983 | ||||||
chr7:889983
|
T | TCTGGGAG others(348): Show |
2 | a0001c0005t0001g0273a0001c0008t0001g0274 | 2 | HG01168.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.467-927_467-926ins others(355): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889983 | |||||
chr7:889997
|
G | C | 2 | a0001c0001t0004g0164a0001c0001t0004g0165 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.467-931G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889997 | ||||||
chr7:890000
|
C | T | 1 | a0001c0002t0001g0105 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.467-928C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890000 | ||||||
chr7:890002
|
C | A | 8 | a0001c0002t0002g0043a0001c0002t0002g0118a0001c0002t0002g0121others(5): Show | 8 | HG02148.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-926C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890002 | ||||||
chr7:890002
|
C | T | 50 | a0001c0002t0001g0025a0001c0002t0001g0027a0001c0002t0001g0093others(47): Show | 56 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.467-926C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890002 | ||||||
chr7:890002
|
CGAGCGGG others(390): Show |
C | 2 | a0001c0001t0001g0008a0001c0001t0001g0228 | 5 | HG02886.hp2 HG02895.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-906_467-510del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890002 | |||||
chr7:890003
|
G | A | 4 | a0001c0001t0014g0055a0001c0002t0006g0050a0001c0003t0006g0038others(1): Show | 5 | HG01496.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-925G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890003 | ||||||
chr7:890006
|
C | T | 2 | a0001c0002t0002g0118a0001c0015t0002g0096 | 2 | NA18522.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.467-922C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890006 | ||||||
chr7:890013
|
T | C | 31 | a0001c0001t0001g0073a0001c0001t0001g0090a0001c0001t0001g0249others(28): Show | 34 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.467-915T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890013 | ||||||
chr7:890013
|
TAGGACGG others(395): Show |
T | 1 | a0001c0002t0002g0118 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.467-914_467-513del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890013 | ||||||
chr7:890018
|
CG | C | 8 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0081others(5): Show | 8 | HG00621.hp2 HG02148.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-906delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890018 | |||||
chr7:890019
|
G | GGGGCCTG others(511): Show |
1 | a0001c0001t0002g0022 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.467-906_467-905ins others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890019
|
G | GGGGTCTG others(631): Show |
1 | a0001c0001t0001g0073 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.467-876_467-875ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890019
|
G | GGGGTCTG others(591): Show |
1 | a0001c0001t0001g0090 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.467-876_467-875ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890019
|
G | GGGGTCTG others(271): Show |
1 | a0001c0001t0002g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.467-876_467-875ins others(278): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890019
|
G | GGGGTCTG others(310): Show |
1 | a0001c0005t0011g0291 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.467-836_467-835ins others(317): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890019
|
G | GGGGTCTG others(111): Show |
1 | a0001c0001t0001g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.467-866_467-749dup others(118): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890019
|
G | GGGGTCTG others(1346): Show |
1 | a0001c0002t0001g0157 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.467-887_467-886ins others(1353): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890019
|
G | GGGGTCTG others(1346): Show |
1 | a0001c0002t0002g0152 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.467-887_467-886ins others(1353): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890019
|
G | GGGTCTGG others(269): Show |
1 | a0001c0009t0001g0042 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.467-907_467-906ins others(276): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890019
|
G | GGGTCTGG others(308): Show |
1 | a0001c0008t0001g0272 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-907_467-906ins others(315): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | |||||
chr7:890023
|
T | C | 17 | a0001c0001t0002g0258a0001c0001t0002g0261a0001c0001t0004g0253others(14): Show | 19 | HG01346.hp2 HG01496.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.467-905T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890023 | ||||||
chr7:890041
|
G | A | 1 | a0001c0002t0021g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.467-887G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890041 | ||||||
chr7:890042
|
C | A | 2 | a0001c0002t0002g0146a0001c0017t0002g0049 | 2 | HG02615.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.467-886C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890042 | ||||||
chr7:890042
|
C | T | 18 | a0001c0002t0001g0141a0001c0002t0001g0144a0001c0002t0001g0147others(15): Show | 18 | HG00544.hp1 HG01081.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-886C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890042 | ||||||
chr7:890043
|
G | A | 7 | a0001c0002t0001g0027a0001c0002t0001g0130a0001c0002t0001g0132others(4): Show | 7 | HG02056.hp2 HG02074.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-885G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890043 | ||||||
chr7:890053
|
T | C | 27 | a0001c0002t0002g0121a0001c0003t0002g0041a0001c0003t0002g0244others(24): Show | 29 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.467-875T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890053 | ||||||
chr7:890058
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.467-870C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890058 | ||||||
chr7:890063
|
T | C | 56 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(53): Show | 62 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.467-865T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890063 | ||||||
chr7:890081
|
G | GGGGGTAG others(5): Show |
1 | a0001c0001t0001g0066 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.467-847_467-846ins others(12): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890081 | ||||||
chr7:890082
|
C | A | 5 | a0001c0002t0002g0121a0001c0002t0002g0159a0001c0015t0002g0096others(2): Show | 5 | HG02148.hp2 HG02615.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-846C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890082 | ||||||
chr7:890082
|
C | T | 17 | a0001c0001t0001g0066a0001c0001t0001g0241a0001c0002t0001g0115others(14): Show | 17 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(14): Show |
intron_variant | MODIFIER | c.467-846C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890082 | ||||||
chr7:890093
|
T | C | 31 | a0001c0002t0001g0115a0001c0002t0002g0092a0001c0002t0002g0106others(28): Show | 33 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.467-835T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890093 | ||||||
chr7:890098
|
C | CG | 98 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0078others(95): Show | 107 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.467-827dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGCCT others(352): Show |
3 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122 | 4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-827_467-826ins others(359): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGCCT others(2022): Show |
1 | a0001c0002t0002g0156 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.467-827_467-826ins others(2029): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGCCT others(2022): Show |
1 | a0001c0002t0002g0140 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.467-827_467-826ins others(2029): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGCCT others(2022): Show |
1 | a0001c0002t0001g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.467-827_467-826ins others(2029): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGTCT others(234): Show |
1 | a0001c0002t0003g0094 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.467-827_467-826ins others(241): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGTCT others(312): Show |
4 | a0001c0002t0001g0027a0001c0002t0001g0132a0001c0002t0001g0133others(1): Show | 4 | HG02056.hp2 NA18747.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-827_467-826ins others(319): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGTCT others(312): Show |
3 | a0001c0002t0002g0099a0001c0002t0002g0101a0001c0002t0035g0117 | 3 | HG02083.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.467-827_467-826ins others(319): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGTCT others(312): Show |
1 | a0001c0002t0001g0100 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.467-827_467-826ins others(319): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGTCT others(588): Show |
1 | a0001c0002t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.467-827_467-826ins others(595): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890098
|
C | CGGGGTCT others(1148): Show |
1 | a0001c0002t0007g0143 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.467-827_467-826ins others(1155): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | |||||
chr7:890102
|
T | C | 22 | a0001c0001t0014g0054a0001c0002t0001g0144a0001c0002t0021g0127others(19): Show | 24 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.467-826T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890102 | ||||||
chr7:890121
|
C | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(112): Show | 156 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.467-807C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890121 | ||||||
chr7:890121
|
C | T | 8 | a0001c0002t0001g0157a0001c0002t0002g0092a0001c0002t0002g0106others(5): Show | 8 | HG01496.hp1 HG02148.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-807C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890121 | ||||||
chr7:890122
|
G | A | 2 | a0001c0010t0025g0053a0001c0010t0026g0052 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.467-806G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890122 | ||||||
chr7:890132
|
T | C | 28 | a0001c0002t0002g0092a0001c0002t0002g0106a0001c0002t0002g0131others(25): Show | 30 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.467-796T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890132 | ||||||
chr7:890134
|
G | GGACGGGG others(231): Show |
1 | a0001c0001t0003g0064 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(238): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890134 | |||||
chr7:890137
|
C | CG | 87 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0229others(84): Show | 96 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.467-788dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | |||||
chr7:890137
|
C | CGGGGTCT others(1030): Show |
1 | a0001c0002t0002g0145 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1037): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | |||||
chr7:890137
|
C | CGGGGTCT others(1109): Show |
1 | a0001c0002t0001g0148 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1116): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | |||||
chr7:890137
|
C | CGGGGTCT others(1030): Show |
1 | a0001c0002t0002g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1037): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | |||||
chr7:890137
|
C | CGGGGTCT others(1029): Show |
1 | a0001c0002t0002g0155 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1036): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | |||||
chr7:890137
|
C | CGGGGTCT others(1029): Show |
5 | a0001c0002t0001g0141a0001c0002t0002g0153a0001c0002t0002g0154others(2): Show | 5 | HG00544.hp1 HG02132.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-788_467-787ins others(1036): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | |||||
chr7:890137
|
C | CGGGGTCT others(1823): Show |
1 | a0001c0002t0002g0150 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1830): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | |||||
chr7:890137
|
C | CGGGGTCT others(1822): Show |
1 | a0001c0002t0002g0136 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.467-788_467-787ins others(1829): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | |||||
chr7:890137
|
C | CGGGGTCT others(989): Show |
1 | a0001c0002t0002g0142 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.467-788_467-787ins others(996): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | |||||
chr7:890141
|
T | C | 19 | a0001c0002t0001g0147a0001c0002t0002g0140a0001c0002t0002g0156others(16): Show | 21 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.467-787T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890141 | ||||||
chr7:890160
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0002g0196a0001c0015t0002g0096 | 4 | HG01261.hp2 HG02273.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-768C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890160 | ||||||
chr7:890160
|
C | T | 49 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(46): Show | 55 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.467-768C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890160 | ||||||
chr7:890160
|
CGAGCGGG others(232): Show |
C | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(98): Show | 141 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.467-748_467-510del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890160 | |||||
chr7:890171
|
T | C | 60 | a0001c0002t0001g0025a0001c0002t0001g0093a0001c0002t0001g0102others(57): Show | 67 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.467-757T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890171 | ||||||
chr7:890176
|
C | CG | 75 | a0001c0001t0001g0280a0001c0001t0014g0054a0001c0001t0014g0055others(72): Show | 83 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.467-749dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGCCT others(34): Show |
2 | a0001c0003t0002g0270a0001c0003t0002g0284 | 2 | HG00280.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.467-749_467-748ins others(41): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGCCT others(74): Show |
1 | a0001c0003t0002g0269 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.467-749_467-748ins others(81): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGTCT others(748): Show |
1 | a0001c0002t0002g0146 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(755): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGTCT others(1387): Show |
1 | a0001c0002t0001g0144 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(1394): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGTCT others(113): Show |
1 | a0001c0006t0002g0276 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(120): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGTCT others(273): Show |
1 | a0001c0005t0011g0277 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.467-749_467-748ins others(280): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGTCT others(1902): Show |
1 | a0001c0002t0002g0138 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(1909): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGTCT others(1902): Show |
1 | a0001c0002t0002g0158 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(1909): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGTCT others(1228): Show |
2 | a0001c0002t0002g0151a0001c0002t0002g0161 | 2 | NA18947.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.467-749_467-748ins others(1235): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGTCT others(1902): Show |
1 | a0001c0002t0002g0137 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(1909): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890176
|
C | CGGGGTCT others(311): Show |
3 | a0001c0002t0001g0115a0001c0002t0003g0095a0001c0002t0003g0125 | 3 | NA18950.hp2 NA18979.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.467-749_467-748ins others(318): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | |||||
chr7:890180
|
T | C | 22 | a0001c0002t0001g0144a0001c0002t0001g0157a0001c0002t0002g0136others(19): Show | 23 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.467-748T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890180 | ||||||
chr7:890180
|
T | TCTGGGAG others(389): Show |
1 | a0001c0002t0006g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.467-719_467-718ins others(396): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890180 | |||||
chr7:890199
|
C | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0229 | 5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-729C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890199 | ||||||
chr7:890199
|
C | T | 9 | a0001c0002t0002g0043a0001c0002t0002g0121a0001c0005t0040g0265others(6): Show | 9 | HG01891.hp1 HG02148.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-729C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890199 | ||||||
chr7:890199
|
CGAGCGGG others(193): Show |
C | 2 | a0001c0001t0001g0030a0001c0001t0002g0196 | 3 | HG01261.hp2 HG02273.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.467-709_467-510del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890199 | |||||
chr7:890203
|
C | T | 3 | a0001c0002t0002g0121a0001c0017t0002g0049a0001c0019t0001g0126 | 3 | HG02148.hp2 HG02615.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.467-725C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890203 | ||||||
chr7:890210
|
T | C | 44 | a0001c0002t0001g0115a0001c0002t0001g0147a0001c0002t0002g0092others(41): Show | 46 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.467-718T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890210 | ||||||
chr7:890210
|
T | TAGGACGG others(1780): Show |
1 | a0001c0006t0023g0266 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.467-690_467-689ins others(1787): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890210 | |||||
chr7:890215
|
CG | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0090a0001c0001t0001g0215others(4): Show | 9 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-709delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890215 | |||||
chr7:890216
|
G | GGGTCTGG others(388): Show |
3 | a0001c0002t0001g0130a0001c0002t0001g0134a0001c0002t0003g0128 | 3 | HG02074.hp1 NA18953.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.467-710_467-709ins others(395): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | |||||
chr7:890216
|
G | GGGTCTGG others(389): Show |
1 | a0001c0002t0002g0113 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.467-710_467-709ins others(396): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | |||||
chr7:890216
|
G | GGGTCTGG others(388): Show |
9 | a0001c0002t0001g0025a0001c0002t0001g0108a0001c0002t0001g0109others(6): Show | 9 | HG00558.hp1 HG02040.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.467-710_467-709ins others(395): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | |||||
chr7:890216
|
G | GGGTCTGG others(388): Show |
15 | a0001c0002t0001g0093a0001c0002t0001g0102a0001c0002t0001g0116others(12): Show | 20 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.467-710_467-709ins others(395): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | |||||
chr7:890216
|
G | GGGTCTGG others(468): Show |
1 | a0001c0002t0001g0105 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.467-710_467-709ins others(475): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | |||||
chr7:890216
|
G | GGGTCTGG others(111): Show |
1 | a0001c0015t0002g0096 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.467-710_467-709ins others(118): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | |||||
chr7:890216
|
G | GGGTCTGG others(389): Show |
1 | a0001c0002t0003g0129 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.467-710_467-709ins others(396): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | |||||
chr7:890220
|
T | C | 49 | a0001c0002t0001g0025a0001c0002t0001g0093a0001c0002t0001g0102others(46): Show | 55 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.467-708T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890220 | ||||||
chr7:890220
|
T | TCTGGGAG others(190): Show |
1 | a0001c0021t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.467-690_467-689ins others(197): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | |||||
chr7:890220
|
T | TCTGGGAG others(29): Show |
1 | a0001c0017t0002g0049 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-679_467-678ins others(36): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | |||||
chr7:890220
|
T | TCTGGGAG others(349): Show |
1 | a0001c0002t0021g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.467-690_467-689ins others(356): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | |||||
chr7:890220
|
T | TCTGGGAG others(71): Show |
1 | a0001c0002t0003g0094 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.467-690_467-689ins others(78): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | |||||
chr7:890220
|
T | TCTGGGAG others(72): Show |
1 | a0001c0002t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.467-690_467-689ins others(79): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | |||||
chr7:890220
|
T | TCTGGGAG others(349): Show |
3 | a0001c0002t0002g0092a0001c0002t0002g0106a0001c0002t0002g0131 | 3 | HG02896.hp1 HG03579.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.467-690_467-689ins others(356): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | |||||
chr7:890220
|
T | TCTGGGAG others(72): Show |
8 | a0001c0002t0001g0027a0001c0002t0001g0100a0001c0002t0001g0132others(5): Show | 8 | HG01361.hp1 HG02056.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-690_467-689ins others(79): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | |||||
chr7:890220
|
T | TCTGGGAG others(72): Show |
3 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122 | 4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-690_467-689ins others(79): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | |||||
chr7:890239
|
C | T | 5 | a0001c0002t0002g0159a0001c0002t0002g0162a0001c0010t0025g0053others(2): Show | 5 | HG00621.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-689C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890239 | ||||||
chr7:890239
|
CGAGCGGG others(153): Show |
C | 3 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0229 | 5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-669_467-510del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890239 | |||||
chr7:890250
|
T | C | 110 | a0001c0001t0001g0081a0001c0001t0001g0246a0001c0001t0001g0278others(107): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.467-678T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890250 | ||||||
chr7:890250
|
T | TAGGACGG others(1106): Show |
1 | a0001c0005t0040g0265 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.467-670_467-669ins others(1113): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890250 | |||||
chr7:890250
|
T | TAGGACGG others(150): Show |
1 | a0001c0001t0001g0280 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.467-670_467-669ins others(157): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890250 | |||||
chr7:890255
|
CGGGGTCT others(114): Show |
C | 2 | a0001c0003t0006g0038a0001c0011t0002g0045 | 3 | HG02647.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.467-669_467-549del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890255 | |||||
chr7:890260
|
T | C | 13 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0002t0002g0121others(10): Show | 13 | HG01243.hp2 HG01261.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-668T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890260 | ||||||
chr7:890277
|
C | CGCGAGCG others(192): Show |
1 | a0001c0004t0004g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.467-650_467-649ins others(199): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890277 | |||||
chr7:890277
|
C | CGCGAGCG others(192): Show |
1 | a0001c0004t0004g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.467-650_467-649ins others(199): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890277 | |||||
chr7:890277
|
C | T | 52 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(49): Show | 61 | HG00558.hp2 HG00639.hp2 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.467-651C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890277 | ||||||
chr7:890277
|
CGTGAGCG others(113): Show |
C | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.467-638_467-519del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890277 | |||||
chr7:890279
|
T | C | 95 | a0001c0001t0001g0090a0001c0001t0003g0072a0001c0002t0001g0025others(92): Show | 103 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.467-649T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890279 | ||||||
chr7:890279
|
T | TGAGCGGG others(152): Show |
1 | a0001c0005t0001g0273 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.467-612_467-611ins others(159): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890279
|
T | TGAGCGGG others(827): Show |
1 | a0001c0002t0015g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.467-639_467-638ins others(834): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890279
|
T | TGAGCGGG others(787): Show |
2 | a0001c0002t0007g0143a0001c0002t0007g0160 | 2 | NA18994.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.467-639_467-638ins others(794): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890279
|
T | TGAGCGGG others(667): Show |
1 | a0001c0002t0002g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.467-639_467-638ins others(674): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890279
|
T | TGAGCGGG others(667): Show |
1 | a0001c0002t0001g0157 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.467-639_467-638ins others(674): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890279
|
T | TGAGCGGG others(667): Show |
4 | a0001c0002t0001g0144a0001c0002t0002g0151a0001c0002t0002g0152others(1): Show | 4 | NA18947.hp2 NA18982.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-639_467-638ins others(674): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890279
|
T | TGAGCGGG others(827): Show |
1 | a0001c0002t0002g0145 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.467-639_467-638ins others(834): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890279
|
T | TGAGCGGG others(827): Show |
1 | a0001c0002t0001g0148 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.467-639_467-638ins others(834): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890279
|
T | TGAGCGGG others(827): Show |
3 | a0001c0002t0002g0142a0001c0002t0002g0149a0001c0002t0002g0153 | 3 | NA18939.hp2 NA19068.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.467-639_467-638ins others(834): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890279
|
T | TGAGCGGG others(787): Show |
3 | a0001c0002t0001g0141a0001c0002t0002g0154a0001c0002t0002g0155 | 3 | HG00544.hp1 NA18962.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.467-639_467-638ins others(794): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | |||||
chr7:890290
|
C | T | 37 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(34): Show | 45 | HG00558.hp2 HG00639.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.467-638C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890290 | ||||||
chr7:890300
|
T | C | 1 | a0001c0002t0002g0159 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.467-628T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890300 | ||||||
chr7:890317
|
C | G | 1 | a0001c0008t0001g0274 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.467-611C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890317 | ||||||
chr7:890317
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.467-611C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890317 | ||||||
chr7:890319
|
C | A | 4 | a0001c0002t0002g0043a0001c0010t0025g0053a0001c0010t0026g0052others(1): Show | 4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-609C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890319 | ||||||
chr7:890319
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.467-609C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890319 | ||||||
chr7:890320
|
G | A | 2 | a0001c0002t0001g0026a0001c0002t0001g0122 | 3 | HG02895.hp1 NA20752.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.467-608G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890320 | ||||||
chr7:890323
|
C | T | 4 | a0001c0002t0002g0043a0001c0010t0025g0053a0001c0010t0026g0052others(1): Show | 4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-605C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890323 | ||||||
chr7:890329
|
TCAGGACG others(78): Show |
T | 4 | a0001c0002t0002g0043a0001c0010t0025g0053a0001c0010t0026g0052others(1): Show | 4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-597_467-513del others(85): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890329 | |||||
chr7:890330
|
C | T | 6 | a0001c0001t0001g0090a0001c0002t0002g0159a0001c0003t0001g0170others(3): Show | 6 | HG02647.hp2 HG03209.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-598C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890330 | ||||||
chr7:890335
|
CG | C | 5 | a0001c0003t0002g0046a0001c0006t0002g0267a0001c0006t0002g0289others(2): Show | 5 | HG01168.hp2 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-589delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890335 | |||||
chr7:890340
|
T | C | 1 | a0001c0008t0001g0274 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.467-588T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890340 | ||||||
chr7:890357
|
T | C | 36 | a0001c0001t0001g0090a0001c0002t0002g0136a0001c0002t0002g0150others(33): Show | 38 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.467-571T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890357 | ||||||
chr7:890359
|
C | A | 2 | a0001c0003t0002g0046a0001c0003t0002g0169 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.467-569C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890359 | ||||||
chr7:890359
|
C | CGAGCGGG others(193): Show |
1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.467-559_467-558ins others(200): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890359 | |||||
chr7:890359
|
C | T | 1 | a0001c0008t0001g0272 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-569C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890359 | ||||||
chr7:890370
|
C | T | 5 | a0001c0002t0002g0159a0001c0003t0001g0170a0001c0003t0002g0046others(2): Show | 5 | HG02647.hp2 HG03209.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-558C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890370 | ||||||
chr7:890397
|
T | C | 32 | a0001c0002t0002g0159a0001c0003t0001g0170a0001c0003t0002g0041others(29): Show | 35 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.467-531T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890397 | ||||||
chr7:890397
|
T | G | 1 | a0001c0008t0001g0272 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-531T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890397 | ||||||
chr7:890399
|
T | A | 2 | a0001c0005t0011g0277a0001c0006t0002g0276 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.467-529T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890399 | ||||||
chr7:890399
|
T | C | 111 | a0001c0001t0001g0090a0001c0001t0014g0054a0001c0001t0014g0055others(108): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.467-529T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890399 | ||||||
chr7:890403
|
C | T | 2 | a0001c0005t0011g0277a0001c0006t0002g0276 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.467-525C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890403 | ||||||
chr7:890410
|
T | C | 17 | a0001c0001t0001g0090a0001c0002t0001g0144a0001c0002t0002g0136others(14): Show | 18 | HG00280.hp2 HG01168.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-518T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890410 | ||||||
chr7:890415
|
C | CG | 14 | a0001c0001t0001g0090a0001c0003t0002g0041a0001c0003t0002g0244others(11): Show | 15 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.467-510dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGCCTG others(307): Show |
1 | a0001c0008t0001g0272 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-493_467-492ins others(314): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(28): Show |
1 | a0001c0002t0006g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(2055): Show |
1 | a0001c0006t0002g0289 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(2062): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(2055): Show |
2 | a0001c0006t0002g0267a0001c0006t0002g0290 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.467-510_467-509ins others(2062): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(68): Show |
1 | a0001c0005t0001g0273 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(75): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(228): Show |
2 | a0001c0008t0001g0274a0001c0009t0001g0268 | 2 | HG01168.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.467-510_467-509ins others(235): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(427): Show |
1 | a0001c0008t0001g0271 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(434): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(1096): Show |
1 | a0001c0002t0002g0159 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(1103): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(387): Show |
2 | a0001c0005t0001g0275a0001c0009t0001g0042 | 3 | HG00280.hp2 HG01175.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.467-510_467-509ins others(394): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(302): Show |
1 | a0001c0002t0002g0151 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(309): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(302): Show |
1 | a0001c0002t0002g0158 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(309): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(108): Show |
53 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(50): Show | 59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.467-510_467-509ins others(115): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(302): Show |
22 | a0001c0002t0001g0141a0001c0002t0001g0144a0001c0002t0001g0147others(19): Show | 22 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.467-510_467-509ins others(309): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(268): Show |
1 | a0001c0005t0011g0291 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(275): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(307): Show |
1 | a0001c0006t0023g0266 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(314): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(68): Show |
1 | a0001c0017t0002g0049 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(75): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(342): Show |
2 | a0001c0002t0002g0136a0001c0002t0002g0150 | 2 | NA18612.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.467-510_467-509ins others(349): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | CGGGGTCT others(146): Show |
1 | a0001c0019t0001g0126 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(153): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | |||||
chr7:890415
|
C | T | 4 | a0001c0002t0002g0043a0001c0010t0025g0053a0001c0010t0026g0052others(1): Show | 4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-513C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890415 | ||||||
chr7:890419
|
C | T | 13 | a0001c0003t0002g0041a0001c0003t0002g0244a0001c0003t0002g0252others(10): Show | 14 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.467-509C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890419 | ||||||
chr7:890436
|
T | C | 14 | a0001c0001t0002g0044a0001c0003t0002g0041a0001c0003t0002g0244others(11): Show | 15 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.467-492T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890436 | ||||||
chr7:890438
|
T | C | 13 | a0001c0003t0002g0041a0001c0003t0002g0244a0001c0003t0002g0252others(10): Show | 14 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.467-490T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890438 | ||||||
chr7:890449
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(116): Show | 165 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.467-479T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890449 | ||||||
chr7:890449
|
T | TAGGACGG others(72): Show |
4 | a0001c0003t0002g0041a0001c0003t0002g0269a0001c0003t0002g0270others(1): Show | 5 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-471_467-470ins others(79): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890449 | |||||
chr7:890449
|
T | TAGGACGG others(112): Show |
8 | a0001c0003t0002g0244a0001c0003t0002g0252a0001c0003t0002g0285others(5): Show | 8 | HG01261.hp1 HG01981.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-471_467-470ins others(119): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890449 | |||||
chr7:890603
|
T | C | 1 | a0001c0001t0002g0022 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.467-325T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890603 | ||||||
chr7:890610
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.467-318T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890610 | ||||||
chr7:890711
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.467-217C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890711 | ||||||
chr7:890727
|
C | T | 2 | a0001c0001t0014g0054a0001c0001t0014g0055 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.467-201C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890727 | ||||||
chr7:891143
|
C | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122 | 4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+77C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891143 | ||||||
chr7:891183
|
C | T | 1 | a0001c0001t0010g0191 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.605+117C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891183 | ||||||
chr7:891212
|
C | G | 1 | a0001c0001t0029g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.605+146C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891212 | ||||||
chr7:891304
|
G | A | 1 | a0001c0002t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.605+238G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891304 | ||||||
chr7:891327
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.605+261C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891327 | ||||||
chr7:891367
|
G | T | 2 | a0001c0001t0001g0202a0001c0001t0022g0225 | 2 | HG00597.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.605+301G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891367 | ||||||
chr7:891384
|
A | G | 4 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0003t0006g0038others(1): Show | 5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.605+318A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891384 | ||||||
chr7:891490
|
G | T | 1 | a0001c0001t0001g0240 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.605+424G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891490 | ||||||
chr7:891501
|
C | T | 1 | a0001c0003t0002g0286 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.605+435C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891501 | ||||||
chr7:891530
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.605+464G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891530 | ||||||
chr7:891675
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.606-603C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891675 | ||||||
chr7:891750
|
C | T | 1 | a0001c0002t0001g0141 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.606-528C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891750 | ||||||
chr7:891766
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.606-512G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891766 | ||||||
chr7:891785
|
G | C | 7 | a0001c0005t0001g0273a0001c0005t0001g0275a0001c0008t0001g0271others(4): Show | 8 | HG00280.hp2 HG01168.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.606-493G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891785 | ||||||
chr7:891804
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.606-474C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891804 | ||||||
chr7:891814
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.606-464G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891814 | ||||||
chr7:891815
|
C | T | 1 | a0001c0002t0002g0104 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.606-463C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891815 | ||||||
chr7:891816
|
T | C | 6 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0002t0006g0050others(3): Show | 7 | HG01243.hp2 HG01496.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.606-462T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891816 | ||||||
chr7:891846
|
CAG | C | 3 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122 | 4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-431_606-430del others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891846 | ||||||
chr7:891867
|
A | G | 8 | a0001c0001t0004g0028a0001c0001t0004g0164a0001c0001t0004g0165others(5): Show | 10 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.606-411A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891867 | ||||||
chr7:891888
|
C | G | 1 | a0001c0002t0003g0128 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.606-390C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891888 | ||||||
chr7:891930
|
G | C | 1 | a0001c0001t0003g0059 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.606-348G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891930 | ||||||
chr7:891939
|
C | T | 1 | a0001c0001t0001g0008 | 4 | HG02886.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-339C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891939 | ||||||
chr7:891967
|
G | C | 4 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0003t0006g0038others(1): Show | 5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.606-311G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891967 | ||||||
chr7:891980
|
G | A | 1 | a0001c0002t0001g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.606-298G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891980 | ||||||
chr7:892010
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0014g0054a0001c0001t0014g0055others(4): Show | 11 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.606-268G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892010 | ||||||
chr7:892023
|
G | A | 83 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0020others(80): Show | 100 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.606-255G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892023 | ||||||
chr7:892132
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0231 | 2 | NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.606-146G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892132 | ||||||
chr7:892169
|
A | G | 8 | a0001c0001t0004g0028a0001c0001t0004g0164a0001c0001t0004g0165others(5): Show | 10 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.606-109A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892169 | ||||||
chr7:892206
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.606-72G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892206 | ||||||
chr7:892224
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.606-54G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892224 | ||||||
chr7:892227
|
CAGA | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0227 | 6 | HG01256.hp2 HG01258.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.606-48_606-46delAA others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 892227 | |||||
chr7:892239
|
C | T | 1 | a0001c0003t0002g0041 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.606-39C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892239 | ||||||
chr7:892253
|
A | C | 1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.606-25A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892253 | ||||||
chr7:892254
|
C | A | 1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.606-24C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892254 | ||||||
chr7:892465
|
T | C | 4 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0003t0006g0038others(1): Show | 5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+47T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892465 | ||||||
chr7:892564
|
G | A | 1 | a0001c0002t0002g0146 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.746+146G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892564 | ||||||
chr7:892593
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.746+175G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892593 | ||||||
chr7:892620
|
C | T | 13 | a0001c0003t0002g0041a0001c0003t0002g0244a0001c0003t0002g0252others(10): Show | 14 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.746+202C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892620 | ||||||
chr7:892631
|
GTGGGTGT others(17): Show |
G | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(104): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.746+217_746+240del others(24): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 892631 | |||||
chr7:892633
|
G | A | 1 | a0001c0001t0029g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.746+215G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892633 | ||||||
chr7:892657
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.746+239G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892657 | ||||||
chr7:892673
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.746+255G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892673 | ||||||
chr7:892794
|
C | T | 1 | a0001c0002t0001g0088 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.746+376C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892794 | ||||||
chr7:892819
|
C | T | 24 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0002g0002others(21): Show | 33 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.746+401C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892819 | ||||||
chr7:892858
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.746+440G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892858 | ||||||
chr7:892882
|
G | C | 10 | a0001c0002t0001g0027a0001c0002t0001g0130a0001c0002t0001g0132others(7): Show | 10 | HG02056.hp2 HG02074.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.746+464G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892882 | ||||||
chr7:892889
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.746+471C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892889 | ||||||
chr7:892937
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058 | 3 | HG02572.hp1 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.746+519G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892937 | ||||||
chr7:892983
|
A | C | 1 | a0001c0002t0035g0117 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.746+565A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892983 | ||||||
chr7:892983
|
A | G | 4 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0003t0006g0038others(1): Show | 5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+565A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892983 | ||||||
chr7:892984
|
AGT | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0184a0002c0007t0001g0015 | 6 | NA18944.hp1 NA18954.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.746+569_746+570del others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 892984 | |||||
chr7:892993
|
G | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 347 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.746+575G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892993 | ||||||
chr7:893020
|
G | GTT | 4 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0003t0006g0038others(1): Show | 5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+602_746+603ins others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893020 | ||||||
chr7:893022
|
G | T | 39 | a0001c0002t0001g0025a0001c0002t0001g0027a0001c0002t0001g0105others(36): Show | 42 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.746+604G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893022 | ||||||
chr7:893047
|
GTT | G | 24 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0002g0002others(21): Show | 33 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.746+630_746+631del others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893047 | ||||||
chr7:893055
|
TGGGCGTG others(28): Show |
T | 1 | a0001c0001t0001g0235 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.746+648_747-640del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893055 | |||||
chr7:893059
|
CGTG | C | 4 | a0001c0001t0004g0028a0001c0001t0004g0164a0001c0001t0004g0165others(1): Show | 5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.746+648_746+650del others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893059 | |||||
chr7:893077
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.746+659C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893077 | ||||||
chr7:893090
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747-650C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893090 | ||||||
chr7:893094
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747-646C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893094 | ||||||
chr7:893101
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747-639A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893101 | ||||||
chr7:893113
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0224 | 2 | HG03225.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.747-627A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893113 | ||||||
chr7:893129
|
CGTG | C | 53 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027others(50): Show | 59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.747-607_747-605del others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893129 | |||||
chr7:893158
|
A | G | 30 | a0001c0002t0001g0088a0001c0002t0001g0133a0001c0002t0001g0141others(27): Show | 30 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.747-582A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893158 | ||||||
chr7:893172
|
T | G | 2 | a0001c0002t0002g0099a0001c0002t0002g0101 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.747-568T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893172 | ||||||
chr7:893172
|
T | TTGCAGGT others(28): Show |
2 | a0001c0001t0001g0219a0001c0001t0001g0231 | 2 | NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.747-548_747-514dup others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893172 | |||||
chr7:893172
|
TTGCAGGT others(98): Show |
T | 1 | a0001c0001t0002g0022 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.747-513_747-409del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893172 | |||||
chr7:893190
|
C | T | 1 | a0001c0001t0008g0188 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.747-550C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893190 | ||||||
chr7:893192
|
C | T | 1 | a0001c0008t0001g0274 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.747-548C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893192 | ||||||
chr7:893196
|
C | T | 1 | a0001c0003t0002g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.747-544C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893196 | ||||||
chr7:893198
|
CGGTGGTG others(28): Show |
C | 7 | a0001c0001t0001g0032a0001c0001t0001g0185a0001c0001t0002g0044others(4): Show | 8 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.747-513_747-479del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893198 | |||||
chr7:893233
|
T | C | 4 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122others(1): Show | 5 | HG02258.hp2 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-507T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893233 | ||||||
chr7:893233
|
T | TGGTGGTG others(28): Show |
4 | a0001c0005t0011g0277a0001c0005t0011g0291a0001c0006t0002g0276others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.747-437_747-403dup others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893233 | |||||
chr7:893233
|
TGGTGGTG others(28): Show |
T | 3 | a0001c0002t0001g0102a0001c0003t0006g0038a0001c0011t0002g0045 | 4 | HG02647.hp1 HG02717.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-437_747-403del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893233 | |||||
chr7:893268
|
C | CGGTGGTG others(494): Show |
2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.747-178_747-177ins others(501): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893268 | |||||
chr7:893268
|
C | CGGTGGTG others(28): Show |
1 | a0001c0001t0001g0223 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.747-444_747-443ins others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893268 | |||||
chr7:893268
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747-472C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893268 | ||||||
chr7:893301
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.747-439C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893301 | ||||||
chr7:893302
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.747-438G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893302 | ||||||
chr7:893330
|
C | T | 2 | a0001c0003t0006g0038a0001c0011t0002g0045 | 3 | HG02647.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.747-410C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893330 | ||||||
chr7:893331
|
G | A | 3 | a0001c0001t0001g0229a0001c0001t0014g0054a0001c0001t0014g0055 | 3 | HG01243.hp2 HG02717.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.747-409G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893331 | ||||||
chr7:893332
|
C | T | 2 | a0001c0003t0006g0038a0001c0011t0002g0045 | 3 | HG02647.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.747-408C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893332 | ||||||
chr7:893332
|
CGGGCGTG others(28): Show |
C | 3 | a0001c0001t0001g0034a0001c0001t0001g0232a0001c0001t0001g0239 | 4 | HG01255.hp2 HG01934.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.747-397_747-363del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893332 | |||||
chr7:893336
|
CGTG | C | 4 | a0001c0001t0001g0085a0001c0001t0002g0193a0001c0001t0010g0191others(1): Show | 4 | HG02280.hp2 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-395_747-393del others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893336 | |||||
chr7:893338
|
T | C | 6 | a0001c0001t0001g0223a0001c0002t0001g0026a0001c0002t0001g0120others(3): Show | 7 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-402T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893338 | ||||||
chr7:893346
|
G | A | 4 | a0001c0001t0004g0028a0001c0001t0004g0164a0001c0001t0004g0165others(1): Show | 5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-394G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893346 | ||||||
chr7:893346
|
G | T | 6 | a0001c0001t0001g0223a0001c0002t0001g0026a0001c0002t0001g0120others(3): Show | 7 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-394G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893346 | ||||||
chr7:893347
|
T | G | 6 | a0001c0001t0001g0223a0001c0002t0001g0026a0001c0002t0001g0120others(3): Show | 7 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-393T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893347 | ||||||
chr7:893347
|
T | TTGCAGGT others(28): Show |
48 | a0001c0002t0001g0025a0001c0002t0001g0027a0001c0002t0001g0100others(45): Show | 53 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.747-376_747-375ins others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893347 | |||||
chr7:893347
|
TTGCAGGT others(25): Show |
T | 1 | a0001c0002t0038g0103 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.747-375_747-344del others(32): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893347 | |||||
chr7:893353
|
G | A | 29 | a0001c0002t0001g0088a0001c0002t0001g0141a0001c0002t0001g0144others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.747-387G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893353 | ||||||
chr7:893365
|
T | C | 8 | a0001c0001t0001g0223a0001c0002t0001g0026a0001c0002t0001g0120others(5): Show | 10 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.747-375T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893365 | ||||||
chr7:893367
|
T | C | 6 | a0001c0001t0001g0223a0001c0002t0001g0026a0001c0002t0001g0120others(3): Show | 7 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-373T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893367 | ||||||
chr7:893371
|
C | CGCG | 2 | a0001c0003t0006g0038a0001c0011t0002g0045 | 3 | HG02647.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.747-368_747-367ins others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893371 | |||||
chr7:893376
|
T | TG | 5 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122others(2): Show | 6 | HG02148.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.747-363dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893376 | |||||
chr7:893379
|
G | GGT | 5 | a0001c0002t0001g0026a0001c0002t0001g0120a0001c0002t0001g0122others(2): Show | 6 | HG02148.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.747-361_747-360ins others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893379 | ||||||
chr7:893399
|
T | C | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-341T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893399 | ||||||
chr7:893434
|
C | T | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-306C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893434 | ||||||
chr7:893435
|
A | G | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-305A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893435 | ||||||
chr7:893439
|
A | G | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-301A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893439 | ||||||
chr7:893463
|
C | T | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-277C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893463 | ||||||
chr7:893467
|
C | T | 58 | a0001c0001t0002g0222a0001c0001t0002g0258a0001c0001t0002g0261others(55): Show | 64 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.747-273C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893467 | ||||||
chr7:893476
|
T | G | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-264T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893476 | ||||||
chr7:893478
|
GTGCAGGT others(25): Show |
G | 45 | a0001c0002t0001g0025a0001c0002t0001g0027a0001c0002t0001g0100others(42): Show | 50 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.747-242_747-211del others(32): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893478 | |||||
chr7:893485
|
TGAGTGTT others(27): Show |
T | 1 | a0001c0002t0020g0098 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.747-253_747-220del others(34): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893485 | |||||
chr7:893493
|
G | A | 12 | a0001c0003t0002g0041a0001c0003t0002g0244a0001c0003t0002g0252others(9): Show | 13 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.747-247G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893493 | ||||||
chr7:893499
|
G | A | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-241G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893499 | ||||||
chr7:893503
|
ATGGTGGT others(25): Show |
A | 2 | a0001c0002t0001g0093a0001c0002t0001g0102 | 2 | HG02602.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.747-229_747-198del others(32): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893503 | |||||
chr7:893510
|
TTGCAGGT others(28): Show |
T | 1 | a0001c0001t0001g0176 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.747-212_747-178del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893510 | |||||
chr7:893516
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.747-224G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893516 | ||||||
chr7:893528
|
T | C | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-212T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893528 | ||||||
chr7:893530
|
T | C | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-210T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893530 | ||||||
chr7:893531
|
A | G | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-209A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893531 | ||||||
chr7:893531
|
AGGCGTGG others(92): Show |
A | 1 | a0001c0021t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.747-175_747-77delT others(98): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893531 | |||||
chr7:893534
|
C | T | 3 | a0001c0001t0001g0081a0001c0002t0038g0103a0001c0019t0001g0126 | 3 | HG02148.hp2 HG03225.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.747-206C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893534 | ||||||
chr7:893535
|
G | T | 11 | a0001c0001t0002g0258a0001c0001t0002g0261a0001c0001t0004g0253others(8): Show | 12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.747-205G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893535 | ||||||
chr7:893536
|
T | C | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-204T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893536 | ||||||
chr7:893543
|
G | T | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-197G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893543 | ||||||
chr7:893563
|
C | T | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-177C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893563 | ||||||
chr7:893596
|
A | G | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-144A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893596 | ||||||
chr7:893597
|
T | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(198): Show | 247 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.747-143T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893597 | ||||||
chr7:893598
|
G | A | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-142G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893598 | ||||||
chr7:893601
|
C | CACG | 25 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0002g0002others(22): Show | 34 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.747-139_747-138ins others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893601 | ||||||
chr7:893603
|
C | CGGT | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 324 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.747-135_747-133dup others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893603 | |||||
chr7:893603
|
C | CGGTGGTG others(98): Show |
1 | a0001c0001t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747-133_747-132ins others(105): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893603 | |||||
chr7:893603
|
C | T | 29 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0002g0002others(26): Show | 38 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.747-137C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893603 | ||||||
chr7:893608
|
T | G | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-132T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893608 | ||||||
chr7:893609
|
G | T | 2 | a0001c0002t0038g0103a0001c0019t0001g0126 | 2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-131G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893609 | ||||||
chr7:893655
|
T | C | 5 | a0001c0001t0014g0054a0001c0001t0014g0055a0001c0003t0002g0169others(2): Show | 6 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.747-85T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893655 | ||||||
chr7:893710
|
C | G | 1 | a0001c0003t0002g0169 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.747-30C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893710 | ||||||
chr7:893732
|
T | C | 26 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0002g0002others(23): Show | 36 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(33): Show |
splice_region_variant&intron_variant | LOW | c.747-8T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893732 | ||||||
chr7:893861
|
G | C | 1 | a0001c0003t0002g0286 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.823-38G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 7/8 | chr7 | 893861 | ||||||
chr7:893984
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0002g0236 | 5 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.895+13G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 893984 | ||||||
chr7:893997
|
C | T | 1 | a0001c0004t0004g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.895+26C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 893997 | ||||||
chr7:894014
|
C | T | 1 | a0001c0002t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.895+43C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894014 | ||||||
chr7:894034
|
T | C | 1 | a0001c0001t0013g0189 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895+63T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894034 | ||||||
chr7:894058
|
C | T | 1 | a0001c0003t0002g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.895+87C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894058 | ||||||
chr7:894112
|
T | C | 2 | a0001c0003t0002g0046a0001c0017t0002g0049 | 2 | HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.895+141T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894112 | ||||||
chr7:894121
|
A | ATTATTAG others(23): Show |
1 | a0001c0001t0002g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.895+151_895+180dup others(30): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 894121 | |||||
chr7:894121
|
A | ATTATTAG others(53): Show |
1 | a0001c0003t0006g0038 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.895+180_895+181ins others(60): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 894121 | |||||
chr7:894161
|
C | T | 1 | a0001c0001t0029g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.895+190C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894161 | ||||||
chr7:894181
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.895+210A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894181 | ||||||
chr7:894209
|
A | G | 1 | a0001c0021t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.895+238A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894209 | ||||||
chr7:894211
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.895+240T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894211 | ||||||
chr7:894254
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.895+283C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894254 | ||||||
chr7:894267
|
G | A | 3 | a0001c0010t0025g0053a0001c0010t0026g0052a0001c0010t0028g0051 | 3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.895+296G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894267 | ||||||
chr7:894286
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.895+315G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894286 | ||||||
chr7:894307
|
C | T | 1 | a0001c0004t0002g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.895+336C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894307 | ||||||
chr7:894321
|
G | A | 1 | a0001c0003t0006g0038 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.895+350G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894321 | ||||||
chr7:894343
|
C | T | 1 | a0001c0003t0002g0294 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.895+372C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894343 | ||||||
chr7:894357
|
C | T | 29 | a0001c0001t0029g0192a0001c0002t0001g0088a0001c0002t0001g0141others(26): Show | 29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.895+386C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894357 | ||||||
chr7:894360
|
G | A | 1 | a0001c0001t0002g0022 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.895+389G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894360 | ||||||
chr7:894367
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.895+396C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894367 | ||||||
chr7:894394
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.895+423G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894394 | ||||||
chr7:894435
|
C | A | 3 | a0001c0002t0001g0108a0001c0002t0001g0109a0001c0002t0003g0111 | 3 | HG02040.hp2 HG02135.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.895+464C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894435 | ||||||
chr7:894441
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG00558.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.895+470G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894441 | ||||||
chr7:894552
|
C | T | 2 | a0001c0001t0001g0226a0001c0002t0001g0124 | 2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.895+581C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894552 | ||||||
chr7:894558
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.895+587C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894558 | ||||||
chr7:894561
|
A | G | 2 | a0001c0010t0025g0053a0001c0010t0028g0051 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.895+590A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894561 | ||||||
chr7:894630
|
C | T | 1 | a0001c0003t0002g0244 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.895+659C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894630 | ||||||
chr7:894649
|
G | A | 1 | a0001c0002t0001g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.895+678G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894649 | ||||||
chr7:894670
|
G | A | 1 | a0001c0001t0033g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.896-664G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894670 | ||||||
chr7:894692
|
G | T | 5 | a0001c0001t0003g0006a0001c0001t0003g0070a0001c0001t0003g0071others(2): Show | 8 | HG02071.hp2 HG02129.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.896-642G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894692 | ||||||
chr7:894717
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.896-617G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894717 | ||||||
chr7:894718
|
T | G | 1 | a0001c0001t0033g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.896-616T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894718 | ||||||
chr7:894720
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.896-614G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894720 | ||||||
chr7:894748
|
G | A | 1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.896-586G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894748 | ||||||
chr7:894770
|
C | T | 20 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0063others(17): Show | 29 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.896-564C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894770 | ||||||
chr7:894856
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(54): Show | 69 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.896-478A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894856 | ||||||
chr7:894868
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.896-466G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894868 | ||||||
chr7:894892
|
C | T | 24 | a0001c0002t0001g0141a0001c0002t0001g0144a0001c0002t0001g0148others(21): Show | 24 | HG00544.hp1 HG00621.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.896-442C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894892 | ||||||
chr7:894893
|
G | T | 2 | a0001c0001t0012g0180a0001c0001t0012g0186 | 2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.896-441G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894893 | ||||||
chr7:894921
|
C | G | 1 | a0001c0001t0002g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.896-413C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894921 | ||||||
chr7:894938
|
C | T | 2 | a0001c0003t0001g0170a0001c0003t0002g0046 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.896-396C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894938 | ||||||
chr7:894939
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.896-395G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894939 | ||||||
chr7:894943
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.896-391T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894943 | ||||||
chr7:894973
|
A | T | 1 | a0001c0001t0027g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.896-361A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894973 | ||||||
chr7:894985
|
G | A | 2 | a0001c0002t0001g0026a0001c0002t0001g0120 | 3 | HG02615.hp2 HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.896-349G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894985 | ||||||
chr7:895005
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.896-329T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895005 | ||||||
chr7:895088
|
C | T | 7 | a0001c0005t0001g0273a0001c0005t0001g0275a0001c0008t0001g0271others(4): Show | 8 | HG00280.hp2 HG01168.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.896-246C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895088 | ||||||
chr7:895137
|
T | C | 3 | a0001c0003t0001g0170a0001c0003t0002g0046a0001c0003t0010g0168 | 3 | HG02647.hp2 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.896-197T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895137 | ||||||
chr7:895188
|
T | C | 2 | a0001c0017t0002g0049a0001c0021t0002g0097 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.896-146T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895188 | ||||||
chr7:895197
|
G | A | 7 | a0001c0001t0001g0177a0001c0001t0003g0006a0001c0001t0003g0070others(4): Show | 10 | HG01891.hp2 HG02071.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.896-137G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895197 | ||||||
chr7:895211
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.896-123T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895211 | ||||||
chr7:895267
|
G | A | 1 | a0001c0003t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.896-67G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895267 |