geneid | 6936 |
---|---|
ensemblid | ENSG00000005436.14 |
hgncid | 1317 |
symbol | GCFC2 |
name | GC-rich sequence DNA-binding factor 2 |
refseq_nuc | NM_003203.5 |
refseq_prot | NP_003194.3 |
ensembl_nuc | ENST00000321027.8 |
ensembl_prot | ENSP00000318690.3 |
mane_status | MANE Select |
chr | chr2 |
start | 75662705 |
end | 75710915 |
strand | - |
ver | v1.2 |
region | chr2:75662705-75710915 |
region5000 | chr2:75657705-75715915 |
regionname0 | GCFC2_chr2_75662705_75710915 |
regionname5000 | GCFC2_chr2_75657705_75715915 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 781 | 166 | 13 | 29 | 100 | 7 | 15 | 82 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002 | 0/0 | 781 | 142 | 24 | 26 | 68 | 5 | 19 | 55 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0003 | 0/0 | 781 | 34 | 32 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0004 | 0/0 | 781 | 32 | 11 | 5 | 10 | 2 | 4 | 9 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0005 | 0/0 | 781 | 5 | 1 | 2 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0006 | 0/0 | 781 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0007 | 0/0 | 781 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0008 | 0/0 | 781 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0009 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0010 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0011 | 0/0 | 781 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0012 | 0/0 | 781 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0013 | 0/0 | 781 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0014 | 0/0 | 781 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0015 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0016 | 0/0 | 781 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0017 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0018 | 0/0 | 781 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0019 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0020 | 0/0 | 781 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0021 | 0/0 | 781 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2346 | 163 | 13 | 27 | 99 | 7 | 15 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0002 | 0/0 | 2346 | 120 | 20 | 20 | 61 | 3 | 16 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0003 | 0/0 | 2346 | 31 | 11 | 4 | 10 | 2 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0004 | 0/0 | 2346 | 31 | 29 | 2 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0005 | 0/0 | 2346 | 22 | 4 | 6 | 7 | 2 | 3 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0006 | 0/0 | 2346 | 5 | 1 | 2 | 0 | 2 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0007 | 0/0 | 2346 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0008 | 0/0 | 2346 | 4 | 0 | 0 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0009 | 0/0 | 2346 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0010 | 0/0 | 2346 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0011 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0012 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0013 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0014 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0015 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0016 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0017 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0018 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0019 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0020 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0021 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0022 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0023 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0024 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0025 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0026 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
c0027 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2022 | 182 | 15 | 37 | 103 | 11 | 14 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0002 | 0/0 | 2022 | 61 | 9 | 11 | 25 | 3 | 13 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0003 | 0/0 | 2022 | 57 | 15 | 9 | 29 | 0 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0004 | 0/0 | 2023 | 51 | 30 | 5 | 10 | 2 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0005 | 0/0 | 2022 | 15 | 14 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0006 | 0/0 | 2022 | 5 | 0 | 0 | 4 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0007 | 0/0 | 2024 | 4 | 2 | 0 | 0 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0008 | 0/0 | 2023 | 3 | 0 | 0 | 1 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0009 | 0/0 | 2022 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0010 | 0/0 | 2022 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0011 | 0/0 | 2022 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0012 | 0/0 | 2022 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0013 | 0/0 | 2022 | 2 | 0 | 0 | 0 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0014 | 0/0 | 2023 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0015 | 0/0 | 2023 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0016 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0017 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0018 | 0/0 | 2023 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0019 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0020 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0021 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0022 | 0/0 | 2021 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0023 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0024 | 0/0 | 2024 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0025 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
t0026 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 14 | 1 | 1 | 10 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0002 | 0/0 | 8 | 0 | 5 | 1 | 1 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0003 | 0/0 | 7 | 0 | 2 | 0 | 1 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0016 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0020 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0042 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2346 | 163 | 13 | 27 | 99 | 7 | 15 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0016 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0018 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0025 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002 | 0/0 | 2346 | 120 | 20 | 20 | 61 | 3 | 16 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0005 | 0/0 | 2346 | 22 | 4 | 6 | 7 | 2 | 3 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0003c0004 | 0/0 | 2346 | 31 | 29 | 2 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0003c0010 | 0/0 | 2346 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0004c0003 | 0/0 | 2346 | 31 | 11 | 4 | 10 | 2 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0004c0013 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0005c0006 | 0/0 | 2346 | 5 | 1 | 2 | 0 | 2 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0006c0009 | 0/0 | 2346 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0007c0007 | 0/0 | 2346 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0008c0008 | 0/0 | 2346 | 4 | 0 | 0 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0009c0011 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0010c0027 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0011c0012 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0012c0026 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0013c0014 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0014c0019 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0015c0015 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0016c0017 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0017c0022 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0018c0021 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0019c0020 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0020c0023 | 0/0 | 2346 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0021c0024 | 0/0 | 2346 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4367 | 146 | 11 | 26 | 90 | 7 | 10 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0001t0002 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0001t0006 | 0/0 | 4367 | 5 | 0 | 0 | 4 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0001t0008 | 0/0 | 4368 | 3 | 0 | 0 | 1 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0001t0011 | 0/0 | 4367 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0001t0012 | 0/0 | 4367 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0001t0013 | 0/0 | 4367 | 2 | 0 | 0 | 0 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0001t0019 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0001t0025 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0016t0001 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0018t0001 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0001c0025t0001 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0002 | 0/0 | 4367 | 52 | 2 | 10 | 24 | 3 | 13 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0003 | 0/0 | 4367 | 55 | 14 | 9 | 29 | 0 | 3 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0009 | 0/0 | 4367 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0010 | 0/0 | 4367 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0014 | 0/0 | 4368 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0015 | 0/0 | 4368 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0017 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0020 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0022 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0002t0023 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0005t0001 | 0/0 | 4367 | 21 | 3 | 6 | 7 | 2 | 3 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0002c0005t0005 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0003c0004t0002 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0003c0004t0004 | 0/0 | 4368 | 18 | 18 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0003c0004t0005 | 0/0 | 4367 | 12 | 11 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0003c0010t0004 | 0/0 | 4368 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0004c0003t0002 | 0/0 | 4367 | 6 | 6 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0004c0003t0004 | 0/0 | 4368 | 22 | 3 | 4 | 9 | 2 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0004c0003t0018 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0004c0003t0021 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0004c0003t0026 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0004c0013t0004 | 0/0 | 4368 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0005c0006t0001 | 0/0 | 4367 | 5 | 1 | 2 | 0 | 2 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0006c0009t0004 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0006c0009t0005 | 0/0 | 4367 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0007c0007t0004 | 0/0 | 4368 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0008c0008t0001 | 0/0 | 4367 | 4 | 0 | 0 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0009c0011t0007 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0010c0027t0003 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0011c0012t0004 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0012c0026t0001 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0013c0014t0007 | 0/0 | 4369 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0014c0019t0001 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0015c0015t0007 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0016c0017t0001 | 0/0 | 4367 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0017c0022t0016 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0018c0021t0007 | 0/0 | 4369 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0019c0020t0002 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0020c0023t0024 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
a0021c0024t0003 | 0/0 | 4367 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | copy fasta | chr2 | 75657705 | 75715915 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 14 | 1 | 1 | 10 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0016 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0012g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0012g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0013g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0019g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0025g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0016t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0018t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0025t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0002 | 0/0 | 8 | 0 | 5 | 1 | 1 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0009g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0010g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0014g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0014g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0015g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0015g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0017g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0020g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0022g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0023g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0010t0004g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0010t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0003 | 0/0 | 7 | 0 | 2 | 0 | 1 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0018g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0021g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0026g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0013t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0005c0006t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0005c0006t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0005c0006t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0006c0009t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0006c0009t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0006c0009t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0006c0009t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0007c0007t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0007c0007t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0008c0008t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0008c0008t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0008c0008t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0009c0011t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0010c0027t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0011c0012t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0012c0026t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0013c0014t0007g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0014c0019t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0015c0015t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0016c0017t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0017c0022t0016g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0018c0021t0007g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0019c0020t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0020c0023t0024g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0021c0024t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | GBR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0034 | EUR | FIN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00408 | hp1 | a0002 | c0005 | t0001 | g0236 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00438 | hp2 | a0004 | c0003 | t0021 | g0068 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00621 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00639 | hp1 | a0004 | c0013 | t0004 | g0056 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00639 | hp2 | a0002 | c0002 | t0020 | g0156 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00735 | hp1 | a0002 | c0002 | t0003 | g0131 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00735 | hp2 | a0003 | c0004 | t0002 | g0286 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00738 | hp1 | a0002 | c0005 | t0001 | g0035 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00738 | hp2 | a0001 | c0001 | t0025 | g0089 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00741 | hp2 | a0002 | c0005 | t0001 | g0021 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01069 | hp2 | a0002 | c0002 | t0003 | g0098 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01070 | hp1 | a0002 | c0002 | t0003 | g0105 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01074 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01099 | hp1 | a0004 | c0003 | t0004 | g0062 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01099 | hp2 | a0002 | c0005 | t0001 | g0176 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0149 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01109 | hp1 | a0020 | c0023 | t0024 | g0269 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01169 | hp1 | a0005 | c0006 | t0001 | g0015 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0097 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01192 | hp2 | a0002 | c0005 | t0001 | g0021 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01243 | hp1 | a0001 | c0016 | t0001 | g0173 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01243 | hp2 | a0003 | c0004 | t0005 | g0292 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01257 | hp2 | a0002 | c0005 | t0001 | g0178 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01261 | hp1 | a0004 | c0003 | t0004 | g0061 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01346 | hp1 | a0004 | c0003 | t0004 | g0003 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01358 | hp1 | a0002 | c0002 | t0003 | g0120 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01361 | hp2 | a0002 | c0005 | t0001 | g0231 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01433 | hp1 | a0005 | c0006 | t0001 | g0084 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0007 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0154 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01515 | hp2 | a0002 | c0005 | t0001 | g0021 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01516 | hp2 | a0005 | c0006 | t0001 | g0015 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01517 | hp1 | a0002 | c0005 | t0001 | g0175 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01517 | hp2 | a0005 | c0006 | t0001 | g0015 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0094 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01884 | hp2 | a0003 | c0004 | t0005 | g0023 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01891 | hp1 | a0003 | c0010 | t0004 | g0043 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01891 | hp2 | a0003 | c0004 | t0005 | g0294 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01943 | hp2 | a0001 | c0025 | t0001 | g0264 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01975 | hp1 | a0004 | c0003 | t0004 | g0003 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0133 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02040 | hp1 | a0002 | c0002 | t0003 | g0018 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02055 | hp1 | a0007 | c0007 | t0004 | g0070 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02055 | hp2 | a0004 | c0003 | t0002 | g0069 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02056 | hp1 | a0002 | c0005 | t0001 | g0165 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02071 | hp1 | a0002 | c0002 | t0014 | g0143 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02080 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02129 | hp2 | a0002 | c0002 | t0017 | g0137 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02145 | hp2 | a0002 | c0005 | t0001 | g0174 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02155 | hp1 | a0001 | c0001 | t0019 | g0265 | EAS | CDX | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02280 | hp1 | a0003 | c0004 | t0005 | g0290 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02280 | hp2 | a0007 | c0007 | t0004 | g0014 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02293 | hp1 | a0002 | c0002 | t0003 | g0107 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02293 | hp2 | a0014 | c0019 | t0001 | g0268 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02451 | hp1 | a0001 | c0001 | t0011 | g0197 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02451 | hp2 | a0003 | c0004 | t0004 | g0279 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02572 | hp1 | a0002 | c0005 | t0001 | g0224 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02602 | hp1 | a0002 | c0005 | t0001 | g0170 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02602 | hp2 | a0004 | c0003 | t0004 | g0003 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02615 | hp1 | a0003 | c0004 | t0004 | g0285 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02615 | hp2 | a0003 | c0004 | t0004 | g0022 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02622 | hp2 | a0002 | c0002 | t0009 | g0296 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0200 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02647 | hp1 | a0003 | c0004 | t0004 | g0280 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02647 | hp2 | a0004 | c0003 | t0002 | g0053 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0049 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02683 | hp2 | a0018 | c0021 | t0007 | g0161 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02698 | hp1 | a0004 | c0003 | t0004 | g0003 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0141 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02717 | hp1 | a0003 | c0010 | t0004 | g0043 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02717 | hp2 | a0003 | c0004 | t0004 | g0281 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02723 | hp1 | a0002 | c0002 | t0009 | g0046 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02723 | hp2 | a0003 | c0004 | t0004 | g0283 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0127 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02738 | hp2 | a0002 | c0005 | t0001 | g0035 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02809 | hp1 | a0004 | c0003 | t0004 | g0073 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02809 | hp2 | a0003 | c0004 | t0005 | g0295 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02818 | hp1 | a0003 | c0004 | t0004 | g0282 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02818 | hp2 | a0006 | c0009 | t0004 | g0273 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02886 | hp1 | a0002 | c0002 | t0009 | g0046 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02886 | hp2 | a0004 | c0003 | t0004 | g0072 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02896 | hp1 | a0003 | c0004 | t0004 | g0288 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02896 | hp2 | a0004 | c0003 | t0002 | g0054 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02897 | hp2 | a0003 | c0004 | t0004 | g0045 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02922 | hp1 | a0019 | c0020 | t0002 | g0123 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02922 | hp2 | a0003 | c0004 | t0004 | g0287 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02965 | hp1 | a0004 | c0003 | t0026 | g0055 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02970 | hp1 | a0002 | c0002 | t0003 | g0095 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02970 | hp2 | a0004 | c0003 | t0002 | g0013 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02976 | hp1 | a0006 | c0009 | t0005 | g0278 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02976 | hp2 | a0002 | c0002 | t0003 | g0103 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03041 | hp1 | a0002 | c0002 | t0023 | g0121 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03041 | hp2 | a0017 | c0022 | t0016 | g0159 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03098 | hp1 | a0002 | c0002 | t0003 | g0096 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03098 | hp2 | a0003 | c0004 | t0004 | g0277 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03130 | hp1 | a0003 | c0004 | t0004 | g0044 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03130 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03139 | hp1 | a0004 | c0003 | t0004 | g0074 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03139 | hp2 | a0004 | c0003 | t0002 | g0013 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03195 | hp1 | a0007 | c0007 | t0004 | g0014 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03195 | hp2 | a0003 | c0004 | t0005 | g0024 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03209 | hp1 | a0002 | c0002 | t0003 | g0102 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03209 | hp2 | a0015 | c0015 | t0007 | g0158 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03225 | hp2 | a0009 | c0011 | t0007 | g0052 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03239 | hp1 | a0013 | c0014 | t0007 | g0160 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03453 | hp1 | a0003 | c0004 | t0004 | g0022 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03453 | hp2 | a0004 | c0003 | t0002 | g0013 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03486 | hp1 | a0003 | c0004 | t0005 | g0024 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03516 | hp1 | a0002 | c0002 | t0003 | g0100 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03516 | hp2 | a0003 | c0010 | t0004 | g0275 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03540 | hp1 | a0006 | c0009 | t0005 | g0289 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03669 | hp1 | a0002 | c0005 | t0001 | g0166 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0148 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0118 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03704 | hp1 | a0001 | c0001 | t0013 | g0026 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0163 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03710 | hp1 | a0004 | c0003 | t0004 | g0003 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0164 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03831 | hp1 | a0004 | c0003 | t0004 | g0003 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0117 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0136 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03927 | hp1 | a0001 | c0001 | t0013 | g0026 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03927 | hp2 | a0021 | c0024 | t0003 | g0108 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0151 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03942 | hp2 | a0002 | c0002 | t0003 | g0113 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0128 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04184 | hp2 | a0001 | c0001 | t0008 | g0207 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04199 | hp1 | a0016 | c0017 | t0001 | g0230 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04199 | hp2 | a0001 | c0001 | t0008 | g0203 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0122 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18522 | hp1 | a0003 | c0004 | t0004 | g0284 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18747 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | CHB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18906 | hp2 | a0003 | c0004 | t0005 | g0023 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18939 | hp2 | a0001 | c0018 | t0001 | g0266 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18940 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18945 | hp2 | a0002 | c0002 | t0010 | g0028 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18947 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18948 | hp2 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18949 | hp2 | a0004 | c0003 | t0004 | g0058 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18950 | hp2 | a0008 | c0008 | t0001 | g0040 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18953 | hp2 | a0001 | c0001 | t0012 | g0202 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18956 | hp1 | a0002 | c0002 | t0003 | g0110 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18957 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18957 | hp2 | a0002 | c0005 | t0001 | g0232 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18964 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18965 | hp1 | a0002 | c0002 | t0010 | g0028 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18968 | hp2 | a0002 | c0002 | t0003 | g0018 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18969 | hp1 | a0002 | c0005 | t0001 | g0179 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18970 | hp1 | a0004 | c0003 | t0004 | g0067 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18972 | hp2 | a0001 | c0001 | t0012 | g0201 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18973 | hp1 | a0002 | c0002 | t0003 | g0119 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18974 | hp2 | a0004 | c0003 | t0004 | g0065 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18979 | hp1 | a0008 | c0008 | t0001 | g0209 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18979 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18980 | hp1 | a0002 | c0002 | t0014 | g0138 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18986 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18990 | hp2 | a0004 | c0003 | t0004 | g0063 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18992 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18992 | hp2 | a0004 | c0003 | t0004 | g0025 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18993 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18993 | hp2 | a0008 | c0008 | t0001 | g0263 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18997 | hp2 | a0002 | c0002 | t0003 | g0099 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18998 | hp1 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19004 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19004 | hp2 | a0008 | c0008 | t0001 | g0040 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19005 | hp1 | a0002 | c0005 | t0001 | g0235 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19006 | hp2 | a0002 | c0002 | t0003 | g0116 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19043 | hp1 | a0003 | c0004 | t0005 | g0024 | AFR | LWK | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0101 | AFR | LWK | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19054 | hp1 | a0004 | c0003 | t0004 | g0064 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19055 | hp1 | a0011 | c0012 | t0004 | g0057 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19056 | hp1 | a0012 | c0026 | t0001 | g0271 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19057 | hp2 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19062 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19063 | hp2 | a0002 | c0002 | t0003 | g0104 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19064 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19065 | hp1 | a0002 | c0002 | t0003 | g0018 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19068 | hp1 | a0002 | c0005 | t0001 | g0234 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19068 | hp2 | a0004 | c0003 | t0004 | g0059 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19074 | hp2 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19079 | hp2 | a0002 | c0002 | t0015 | g0093 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19080 | hp2 | a0004 | c0003 | t0004 | g0025 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19081 | hp1 | a0002 | c0002 | t0015 | g0115 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19082 | hp1 | a0002 | c0002 | t0003 | g0114 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19083 | hp1 | a0004 | c0003 | t0004 | g0066 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19083 | hp2 | a0002 | c0005 | t0001 | g0233 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19087 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19090 | hp1 | a0001 | c0001 | t0008 | g0167 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19091 | hp1 | a0002 | c0002 | t0003 | g0112 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19240 | hp1 | a0003 | c0004 | t0005 | g0291 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19240 | hp2 | a0002 | c0002 | t0003 | g0157 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20129 | hp1 | a0002 | c0005 | t0001 | g0177 | AFR | ASW | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20129 | hp2 | a0003 | c0004 | t0005 | g0023 | AFR | ASW | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20752 | hp1 | a0004 | c0003 | t0004 | g0060 | EUR | TSI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20805 | hp1 | a0004 | c0003 | t0004 | g0003 | EUR | TSI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0162 | SAS | GIH | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | GIH | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02109 | hp1 | a0002 | c0005 | t0005 | g0225 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02109 | hp2 | a0004 | c0003 | t0018 | g0071 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02486 | hp1 | a0003 | c0004 | t0004 | g0276 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02486 | hp2 | a0005 | c0006 | t0001 | g0085 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02559 | hp1 | a0010 | c0027 | t0003 | g0272 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03471 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03471 | hp2 | a0003 | c0004 | t0004 | g0045 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG06807 | hp1 | a0007 | c0007 | t0004 | g0014 | AFR | USA | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG06807 | hp2 | a0003 | c0004 | t0004 | g0044 | AFR | USA | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18955 | hp1 | a0002 | c0002 | t0022 | g0145 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20300 | hp1 | a0003 | c0004 | t0004 | g0022 | AFR | USA | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20300 | hp2 | a0003 | c0004 | t0005 | g0293 | AFR | USA | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA21309 | hp2 | a0006 | c0009 | t0004 | g0274 | AFR | LWK | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0087 | REF | REF | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:75665985
|
T | G | 2 | a0013a0018 | 2 | HG02683.hp2 HG03239.hp1 |
missense_variant | MODERATE | c.2172A>C | p.Glu724Asp | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/17 | 2232/4367 | 2172/2346 | 724/781 | chr2 | 75665985 | ||
chr2:75665999
|
T | C | 1 | a0014 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.2158A>G | p.Ile720Val | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/17 | 2218/4367 | 2158/2346 | 720/781 | chr2 | 75665999 | ||
chr2:75671975
|
T | C | 1 | a0008 | 4 | NA18950.hp2 NA18979.hp1 NA18993.hp2 others(1): Show |
missense_variant | MODERATE | c.1931A>G | p.Glu644Gly | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/17 | 1991/4367 | 1931/2346 | 644/781 | chr2 | 75671975 | ||
chr2:75680221
|
C | G | 1 | a0015 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1784G>C | p.Cys595Ser | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/17 | 1844/4367 | 1784/2346 | 595/781 | chr2 | 75680221 | ||
chr2:75680225
|
T | C | 8 | a0003a0004a0007others(5): Show | 75 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(72): Show |
missense_variant | MODERATE | c.1780A>G | p.Thr594Ala | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/17 | 1840/4367 | 1780/2346 | 594/781 | chr2 | 75680225 | ||
chr2:75680282
|
T | C | 1 | a0017 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1723A>G | p.Thr575Ala | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/17 | 1783/4367 | 1723/2346 | 575/781 | chr2 | 75680282 | ||
chr2:75687860
|
T | C | 1 | a0020 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1657A>G | p.Ile553Val | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/17 | 1717/4367 | 1657/2346 | 553/781 | chr2 | 75687860 | ||
chr2:75687889
|
C | G | 2 | a0016a0021 | 2 | HG03927.hp2 HG04199.hp1 |
missense_variant | MODERATE | c.1628G>C | p.Ser543Thr | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/17 | 1688/4367 | 1628/2346 | 543/781 | chr2 | 75687889 | ||
chr2:75690035
|
G | C | 1 | a0005 | 5 | HG01169.hp1 HG01433.hp1 HG01516.hp2 others(2): Show |
missense_variant | MODERATE | c.1273C>G | p.Gln425Glu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/17 | 1333/4367 | 1273/2346 | 425/781 | chr2 | 75690035 | ||
chr2:75694315
|
G | C | 1 | a0007 | 4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.946C>G | p.Gln316Glu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/17 | 1006/4367 | 946/2346 | 316/781 | chr2 | 75694315 | ||
chr2:75696287
|
T | C | 13 | a0002a0003a0004others(10): Show | 221 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(218): Show |
missense_variant | MODERATE | c.746A>G | p.Asn249Ser | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/17 | 806/4367 | 746/2346 | 249/781 | chr2 | 75696287 | ||
chr2:75702257
|
C | G | 1 | a0011 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.561G>C | p.Lys187Asn | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/17 | 621/4367 | 561/2346 | 187/781 | chr2 | 75702257 | ||
chr2:75702387
|
C | T | 1 | a0013 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.431G>A | p.Arg144His | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/17 | 491/4367 | 431/2346 | 144/781 | chr2 | 75702387 | ||
chr2:75710663
|
G | C | 1 | a0012 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.193C>G | p.Arg65Gly | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 253/4367 | 193/2346 | 65/781 | chr2 | 75710663 | ||
chr2:75710675
|
C | T | 4 | a0004a0007a0009others(1): Show | 38 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(35): Show |
missense_variant | MODERATE | c.181G>A | p.Val61Ile | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 241/4367 | 181/2346 | 61/781 | chr2 | 75710675 | ||
chr2:75710683
|
G | A | 1 | a0010 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.173C>T | p.Pro58Leu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 233/4367 | 173/2346 | 58/781 | chr2 | 75710683 | ||
chr2:75710689
|
C | T | 1 | a0009 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.167G>A | p.Gly56Glu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 227/4367 | 167/2346 | 56/781 | chr2 | 75710689 | ||
chr2:75710762
|
G | C | 2 | a0003a0006 | 38 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(35): Show |
missense_variant | MODERATE | c.94C>G | p.Pro32Ala | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 154/4367 | 94/2346 | 32/781 | chr2 | 75710762 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:75665937
|
A | G | 1 | a0001c0018 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.2220T>C | p.Ser740Ser | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/17 | 2280/4367 | 2220/2346 | 740/781 | chr2 | 75665937 | ||
chr2:75670221
|
G | A | 1 | a0004c0013 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.2020C>T | p.Leu674Leu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/17 | 2080/4367 | 2020/2346 | 674/781 | chr2 | 75670221 | ||
chr2:75687909
|
C | T | 17 | a0001c0016a0002c0002a0003c0004others(14): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
synonymous_variant | LOW | c.1608G>A | p.Val536Val | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/17 | 1668/4367 | 1608/2346 | 536/781 | chr2 | 75687909 | ||
chr2:75691996
|
C | T | 1 | a0003c0010 | 3 | HG01891.hp1 HG02717.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1125G>A | p.Thr375Thr | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/17 | 1185/4367 | 1125/2346 | 375/781 | chr2 | 75691996 | ||
chr2:75706554
|
G | A | 1 | a0001c0025 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.363C>T | p.Ser121Ser | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/17 | 423/4367 | 363/2346 | 121/781 | chr2 | 75706554 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:75662780
|
A | G | 6 | a0002c0002t0003a0002c0002t0010a0002c0002t0015others(3): Show | 62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1886T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1886 | chr2 | 75662780 | |||||
chr2:75662881
|
C | G | 1 | a0002c0002t0020 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1785G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1785 | chr2 | 75662881 | |||||
chr2:75662904
|
T | TA | 16 | a0001c0001t0008a0002c0002t0003a0002c0002t0010others(13): Show | 118 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1761dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1761 | chr2 | 75662904 | |||||
chr2:75662904
|
T | TAA | 7 | a0002c0002t0015a0004c0003t0026a0009c0011t0007others(4): Show | 8 | HG01109.hp1 HG02683.hp2 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1760_*1761dupTT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1761 | chr2 | 75662904 | |||||
chr2:75662920
|
A | C | 1 | a0002c0002t0009 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1746T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1746 | chr2 | 75662920 | |||||
chr2:75662948
|
G | A | 1 | a0002c0002t0023 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1718C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1718 | chr2 | 75662948 | |||||
chr2:75662967
|
A | C | 1 | a0001c0001t0019 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1699 | chr2 | 75662967 | |||||
chr2:75663256
|
A | G | 1 | a0004c0003t0021 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1410T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1410 | chr2 | 75663256 | |||||
chr2:75663264
|
T | G | 1 | a0001c0001t0013 | 2 | HG03704.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1402A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1402 | chr2 | 75663264 | |||||
chr2:75663282
|
A | G | 35 | a0001c0001t0002a0002c0002t0002a0002c0002t0003others(32): Show | 206 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1384T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1384 | chr2 | 75663282 | |||||
chr2:75663414
|
T | C | 35 | a0001c0001t0002a0002c0002t0002a0002c0002t0003others(32): Show | 206 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1252A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1252 | chr2 | 75663414 | |||||
chr2:75663422
|
A | G | 1 | a0001c0001t0012 | 2 | NA18953.hp2 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1244 | chr2 | 75663422 | |||||
chr2:75663702
|
T | A | 27 | a0002c0002t0003a0002c0002t0009a0002c0002t0010others(24): Show | 141 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*964A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 964 | chr2 | 75663702 | |||||
chr2:75663844
|
A | G | 1 | a0004c0003t0018 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 822 | chr2 | 75663844 | |||||
chr2:75663882
|
AT | A | 7 | a0002c0002t0003a0002c0002t0010a0002c0002t0015others(4): Show | 63 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*783delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 783 | chr2 | 75663882 | |||||
chr2:75663967
|
G | A | 1 | a0020c0023t0024 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*699C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 699 | chr2 | 75663967 | |||||
chr2:75663973
|
A | G | 1 | a0001c0001t0011 | 2 | HG02451.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*693T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 693 | chr2 | 75663973 | |||||
chr2:75664123
|
G | A | 1 | a0001c0001t0025 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 543 | chr2 | 75664123 | |||||
chr2:75664144
|
C | T | 1 | a0002c0002t0017 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*522G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 522 | chr2 | 75664144 | |||||
chr2:75664283
|
G | A | 1 | a0004c0003t0026 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 383 | chr2 | 75664283 | |||||
chr2:75664518
|
C | T | 1 | a0017c0022t0016 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*148G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 148 | chr2 | 75664518 | |||||
chr2:75664558
|
C | T | 1 | a0002c0002t0010 | 2 | NA18945.hp2 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*108G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 108 | chr2 | 75664558 | |||||
chr2:75710871
|
G | A | 1 | a0002c0002t0009 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
5_prime_UTR_variant | MODIFIER | c.-16C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 16 | chr2 | 75710871 | |||||
chr2:75710874
|
C | T | 1 | a0001c0001t0006 | 5 | HG02683.hp1 NA18940.hp2 NA18948.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-19G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 19 | chr2 | 75710874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:75664807
|
C | T | 1 | a0002c0002t0002g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2229-24G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75664807 | ||||||
chr2:75664985
|
T | C | 41 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(38): Show | 56 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.2229-202A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75664985 | ||||||
chr2:75665029
|
T | C | 1 | a0017c0022t0016g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2229-246A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665029 | ||||||
chr2:75665061
|
C | T | 25 | a0002c0005t0005g0225a0003c0004t0004g0022a0003c0004t0004g0044others(22): Show | 34 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.2229-278G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665061 | ||||||
chr2:75665193
|
T | C | 149 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(146): Show | 206 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.2229-410A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665193 | ||||||
chr2:75665450
|
G | A | 1 | a0003c0004t0002g0286 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2228+479C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665450 | ||||||
chr2:75665464
|
T | C | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2228+465A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665464 | ||||||
chr2:75665471
|
T | G | 1 | a0006c0009t0004g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2228+458A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665471 | ||||||
chr2:75665486
|
G | A | 69 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(66): Show | 101 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(98): Show |
intron_variant | MODIFIER | c.2228+443C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665486 | ||||||
chr2:75665539
|
C | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2228+390G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665539 | ||||||
chr2:75665545
|
ATTC | A | 2 | a0007c0007t0004g0014a0007c0007t0004g0070 | 4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2228+381_2228+383d others(5): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665545 | ||||||
chr2:75665552
|
A | G | 2 | a0003c0010t0004g0043a0003c0010t0004g0275 | 3 | HG01891.hp1 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2228+377T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665552 | ||||||
chr2:75665696
|
T | C | 2 | a0006c0009t0004g0273a0006c0009t0004g0274 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2228+233A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665696 | ||||||
chr2:75665711
|
T | C | 18 | a0004c0003t0004g0003a0004c0003t0004g0025a0004c0003t0004g0058others(15): Show | 25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.2228+218A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665711 | ||||||
chr2:75665749
|
T | G | 1 | a0004c0003t0004g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2228+180A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665749 | ||||||
chr2:75665801
|
T | C | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2228+128A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665801 | ||||||
chr2:75666110
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2104-57T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666110 | ||||||
chr2:75666131
|
T | C | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2104-78A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666131 | ||||||
chr2:75666169
|
G | C | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2104-116C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666169 | ||||||
chr2:75666177
|
A | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2104-124T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666177 | ||||||
chr2:75666344
|
T | G | 8 | a0003c0004t0004g0044a0003c0004t0004g0045a0003c0004t0004g0276others(5): Show | 11 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2104-291A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666344 | ||||||
chr2:75666355
|
T | A | 1 | a0001c0001t0001g0219 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2104-302A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666355 | ||||||
chr2:75666518
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2104-465A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666518 | ||||||
chr2:75666579
|
G | C | 1 | a0002c0002t0003g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2104-526C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666579 | ||||||
chr2:75666633
|
C | T | 90 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(87): Show | 129 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.2104-580G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666633 | ||||||
chr2:75666727
|
A | AC | 4 | a0002c0002t0002g0127a0002c0002t0002g0135a0002c0002t0002g0139others(1): Show | 4 | HG02738.hp1 NA18943.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.2104-675dupG | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666727 | ||||||
chr2:75666727
|
A | C | 38 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(35): Show | 53 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.2104-674T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666727 | ||||||
chr2:75666786
|
A | G | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2104-733T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666786 | ||||||
chr2:75666832
|
G | C | 1 | a0001c0001t0001g0247 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2104-779C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666832 | ||||||
chr2:75666926
|
T | C | 1 | a0004c0003t0021g0068 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2104-873A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666926 | ||||||
chr2:75666951
|
C | T | 1 | a0002c0002t0017g0137 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2104-898G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666951 | ||||||
chr2:75667099
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(62): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2104-1046A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667099 | ||||||
chr2:75667214
|
CT | C | 3 | a0002c0002t0003g0106a0002c0002t0003g0109a0002c0002t0003g0116 | 3 | HG02080.hp2 NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.2104-1162delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667214 | ||||||
chr2:75667294
|
A | G | 4 | a0004c0003t0004g0058a0004c0003t0004g0059a0004c0003t0004g0064others(1): Show | 4 | NA18949.hp2 NA18970.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.2104-1241T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667294 | ||||||
chr2:75667409
|
T | C | 1 | a0002c0005t0001g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2104-1356A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667409 | ||||||
chr2:75667554
|
C | CCTCA | 9 | a0002c0002t0003g0009a0002c0002t0003g0017a0002c0002t0003g0096others(6): Show | 14 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.2104-1502_2104-150 others(8): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667554 | ||||||
chr2:75667625
|
T | G | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2104-1572A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667625 | ||||||
chr2:75667915
|
T | C | 2 | a0013c0014t0007g0160a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2104-1862A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667915 | ||||||
chr2:75667943
|
A | G | 25 | a0002c0005t0005g0225a0003c0004t0004g0022a0003c0004t0004g0044others(22): Show | 34 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.2104-1890T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667943 | ||||||
chr2:75668136
|
A | G | 16 | a0002c0002t0003g0007a0002c0002t0003g0029a0002c0002t0003g0030others(13): Show | 23 | HG00621.hp1 HG01070.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.2103+2002T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668136 | ||||||
chr2:75668240
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2103+1898G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668240 | ||||||
chr2:75668339
|
G | GAAAAC | 16 | a0001c0001t0001g0004a0001c0001t0001g0092a0001c0001t0001g0181others(13): Show | 22 | HG00609.hp2 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2103+1794_2103+179 others(9): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668339 | ||||||
chr2:75668339
|
G | GAAAACCA others(9): Show |
1 | a0006c0009t0005g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2103+1798_2103+179 others(20): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668339 | ||||||
chr2:75668339
|
G | GAAAACCA others(14): Show |
1 | a0006c0009t0005g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2103+1798_2103+179 others(25): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668339 | ||||||
chr2:75668339
|
GAAAAC | G | 3 | a0002c0002t0009g0046a0002c0002t0009g0296a0004c0003t0026g0055 | 4 | HG02622.hp2 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2103+1794_2103+179 others(9): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668339 | ||||||
chr2:75668778
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2103+1360A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668778 | ||||||
chr2:75668852
|
C | T | 148 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(145): Show | 205 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.2103+1286G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668852 | ||||||
chr2:75668859
|
A | G | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2103+1279T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668859 | ||||||
chr2:75668873
|
C | G | 2 | a0007c0007t0004g0014a0007c0007t0004g0070 | 4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2103+1265G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668873 | ||||||
chr2:75668938
|
C | G | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2103+1200G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668938 | ||||||
chr2:75668967
|
G | A | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2103+1171C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668967 | ||||||
chr2:75669198
|
T | A | 1 | a0002c0002t0003g0116 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2103+940A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669198 | ||||||
chr2:75669343
|
A | G | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2103+795T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669343 | ||||||
chr2:75669504
|
C | A | 41 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(38): Show | 56 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.2103+634G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669504 | ||||||
chr2:75669542
|
T | A | 1 | a0002c0002t0014g0138 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2103+596A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669542 | ||||||
chr2:75669652
|
C | T | 1 | a0002c0005t0001g0235 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2103+486G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669652 | ||||||
chr2:75669775
|
C | G | 7 | a0003c0004t0002g0286a0004c0003t0002g0013a0004c0003t0002g0053others(4): Show | 9 | HG00735.hp2 HG02055.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2103+363G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669775 | ||||||
chr2:75669827
|
C | T | 1 | a0017c0022t0016g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2103+311G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669827 | ||||||
chr2:75669885
|
T | TA | 42 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.2103+252_2103+253i others(3): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669885 | ||||||
chr2:75669886
|
G | C | 42 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.2103+252C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669886 | ||||||
chr2:75669904
|
T | C | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2103+234A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669904 | ||||||
chr2:75669967
|
C | T | 2 | a0007c0007t0004g0014a0007c0007t0004g0070 | 4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2103+171G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669967 | ||||||
chr2:75670050
|
C | G | 99 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(96): Show | 140 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(137): Show |
intron_variant | MODIFIER | c.2103+88G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75670050 | ||||||
chr2:75670073
|
T | C | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2103+65A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75670073 | ||||||
chr2:75670409
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1957-125T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670409 | ||||||
chr2:75670439
|
C | A | 9 | a0002c0005t0005g0225a0003c0004t0005g0023a0003c0004t0005g0024others(6): Show | 13 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1957-155G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670439 | ||||||
chr2:75670460
|
T | C | 2 | a0003c0004t0004g0280a0003c0004t0004g0283 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1957-176A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670460 | ||||||
chr2:75670580
|
C | T | 2 | a0006c0009t0004g0273a0006c0009t0004g0274 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1957-296G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670580 | ||||||
chr2:75670590
|
C | G | 1 | a0001c0001t0001g0254 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1957-306G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670590 | ||||||
chr2:75670756
|
G | A | 2 | a0007c0007t0004g0014a0007c0007t0004g0070 | 4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-472C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670756 | ||||||
chr2:75670763
|
T | C | 3 | a0002c0002t0003g0009a0002c0002t0003g0102a0010c0027t0003g0272 | 6 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1957-479A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670763 | ||||||
chr2:75670813
|
A | C | 49 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(46): Show | 66 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1957-529T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670813 | ||||||
chr2:75670927
|
T | C | 1 | a0002c0002t0003g0104 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1957-643A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670927 | ||||||
chr2:75670939
|
T | C | 1 | a0002c0002t0003g0095 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1957-655A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670939 | ||||||
chr2:75671179
|
T | C | 3 | a0002c0002t0003g0029a0002c0002t0003g0111a0002c0002t0003g0119 | 4 | HG00621.hp1 NA18747.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1956+771A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671179 | ||||||
chr2:75671232
|
C | A | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1956+718G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671232 | ||||||
chr2:75671283
|
G | A | 1 | a0018c0021t0007g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1956+667C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671283 | ||||||
chr2:75671373
|
G | C | 1 | a0003c0004t0005g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1956+577C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671373 | ||||||
chr2:75671475
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1956+475G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671475 | ||||||
chr2:75671610
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1956+340A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671610 | ||||||
chr2:75671764
|
CATTT | C | 92 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(89): Show | 131 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.1956+182_1956+185d others(6): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671764 | ||||||
chr2:75671801
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0220a0001c0001t0001g0227others(1): Show | 10 | NA18942.hp2 NA18952.hp1 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.1956+149G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671801 | ||||||
chr2:75671802
|
G | A | 1 | a0006c0009t0004g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1956+148C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671802 | ||||||
chr2:75671870
|
A | G | 1 | a0004c0003t0004g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1956+80T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671870 | ||||||
chr2:75671902
|
C | A | 1 | a0018c0021t0007g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1956+48G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671902 | ||||||
chr2:75672177
|
A | ATTTATAA others(28): Show |
1 | a0018c0021t0007g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1890-196_1890-162d others(37): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | ||||||
chr2:75672177
|
A | ATTTATAA others(63): Show |
2 | a0013c0014t0007g0160a0017c0022t0016g0159 | 2 | HG03041.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1890-231_1890-162d others(72): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | ||||||
chr2:75672177
|
ATTTATAA others(28): Show |
A | 63 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0012g0201others(60): Show | 91 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.1890-196_1890-162d others(37): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | ||||||
chr2:75672177
|
ATTTATAA others(63): Show |
A | 212 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(209): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1890-231_1890-162d others(72): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | ||||||
chr2:75672177
|
ATTTATAA others(98): Show |
A | 5 | a0001c0001t0001g0092a0002c0002t0002g0124a0002c0002t0002g0146others(2): Show | 5 | HG01109.hp1 HG02895.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1890-266_1890-162d others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | ||||||
chr2:75672178
|
TTTATAAA others(27): Show |
T | 1 | a0002c0002t0003g0099 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1890-196_1890-163d others(36): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672178 | ||||||
chr2:75672235
|
A | AT | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1890-220dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672235 | ||||||
chr2:75672270
|
A | AT | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1890-255dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672270 | ||||||
chr2:75672287
|
TAAAATAT others(64): Show |
T | 1 | a0002c0002t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1890-342_1890-272d others(73): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672287 | ||||||
chr2:75672291
|
ATATATAT others(36): Show |
A | 1 | a0006c0009t0005g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1890-318_1890-276d others(45): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672291 | ||||||
chr2:75672305
|
A | AT | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1890-290dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672305 | ||||||
chr2:75672381
|
A | G | 5 | a0002c0002t0009g0046a0002c0002t0009g0296a0006c0009t0005g0278others(2): Show | 6 | HG02622.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1890-365T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672381 | ||||||
chr2:75672395
|
A | G | 2 | a0006c0009t0004g0273a0006c0009t0004g0274 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1890-379T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672395 | ||||||
chr2:75672570
|
A | G | 2 | a0013c0014t0007g0160a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1890-554T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672570 | ||||||
chr2:75672606
|
C | T | 87 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(84): Show | 124 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1890-590G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672606 | ||||||
chr2:75672658
|
G | A | 1 | a0004c0003t0018g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1890-642C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672658 | ||||||
chr2:75672733
|
C | T | 1 | a0002c0002t0003g0095 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1889+711G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672733 | ||||||
chr2:75672737
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(240): Show | 334 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.1889+707A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672737 | ||||||
chr2:75672784
|
T | G | 1 | a0006c0009t0004g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1889+660A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672784 | ||||||
chr2:75673002
|
T | C | 1 | a0006c0009t0005g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1889+442A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673002 | ||||||
chr2:75673037
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1889+407C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673037 | ||||||
chr2:75673038
|
C | T | 3 | a0001c0001t0001g0211a0001c0001t0012g0201a0001c0001t0012g0202 | 3 | NA18953.hp2 NA18972.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1889+406G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673038 | ||||||
chr2:75673077
|
A | G | 6 | a0001c0001t0001g0168a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 7 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1889+367T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673077 | ||||||
chr2:75673081
|
C | T | 43 | a0001c0001t0001g0172a0001c0001t0002g0214a0002c0002t0002g0002others(40): Show | 58 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1889+363G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673081 | ||||||
chr2:75673085
|
C | T | 43 | a0001c0001t0001g0172a0001c0001t0002g0214a0002c0002t0002g0002others(40): Show | 58 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1889+359G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673085 | ||||||
chr2:75673086
|
G | A | 2 | a0001c0001t0001g0241a0017c0022t0016g0159 | 2 | HG03041.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1889+358C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673086 | ||||||
chr2:75673093
|
A | G | 6 | a0001c0001t0001g0168a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1889+351T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673093 | ||||||
chr2:75673106
|
C | G | 8 | a0001c0001t0001g0168a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 9 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1889+338G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673106 | ||||||
chr2:75673111
|
C | T | 1 | a0004c0003t0018g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1889+333G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673111 | ||||||
chr2:75673113
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0195 | 2 | HG04228.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1889+331T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673113 | ||||||
chr2:75673117
|
T | C | 1 | a0018c0021t0007g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1889+327A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673117 | ||||||
chr2:75673129
|
T | C | 2 | a0004c0003t0018g0071a0009c0011t0007g0052 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1889+315A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673129 | ||||||
chr2:75673138
|
A | G | 13 | a0002c0002t0002g0094a0003c0004t0002g0286a0003c0004t0004g0044others(10): Show | 17 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1889+306T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673138 | ||||||
chr2:75673171
|
G | A | 3 | a0001c0001t0001g0223a0002c0005t0001g0035a0002c0005t0001g0231 | 4 | HG00738.hp1 HG01361.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1889+273C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673171 | ||||||
chr2:75673173
|
G | A | 1 | a0001c0001t0025g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1889+271C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673173 | ||||||
chr2:75673178
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0223a0020c0023t0024g0269 | 3 | HG01109.hp1 HG04204.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1889+266G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673178 | ||||||
chr2:75673179
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0194 | 2 | HG01496.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1889+265C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673179 | ||||||
chr2:75673182
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1889+262G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673182 | ||||||
chr2:75673183
|
G | A | 2 | a0002c0005t0001g0035a0002c0005t0001g0231 | 3 | HG00738.hp1 HG01361.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1889+261C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673183 | ||||||
chr2:75673254
|
G | T | 43 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(40): Show | 58 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1889+190C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673254 | ||||||
chr2:75673264
|
C | T | 1 | a0006c0009t0005g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1889+180G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673264 | ||||||
chr2:75673287
|
G | A | 1 | a0002c0002t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1889+157C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673287 | ||||||
chr2:75673383
|
TAAAC | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1889+57_1889+60del others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673383 | ||||||
chr2:75673392
|
C | T | 1 | a0021c0024t0003g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1889+52G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673392 | ||||||
chr2:75673574
|
C | CA | 49 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(46): Show | 66 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1813-55dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673574 | ||||||
chr2:75673631
|
G | A | 2 | a0013c0014t0007g0160a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1813-111C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673631 | ||||||
chr2:75673677
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1813-157A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673677 | ||||||
chr2:75673789
|
T | C | 97 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(94): Show | 138 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.1813-269A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673789 | ||||||
chr2:75673847
|
A | C | 1 | a0003c0004t0005g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1813-327T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673847 | ||||||
chr2:75673921
|
A | C | 1 | a0001c0001t0001g0241 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1813-401T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673921 | ||||||
chr2:75673924
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0252a0002c0002t0003g0114 | 4 | NA18966.hp1 NA18977.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1813-404G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673924 | ||||||
chr2:75673925
|
G | A | 1 | a0002c0002t0003g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1813-405C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673925 | ||||||
chr2:75673943
|
A | G | 43 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(40): Show | 58 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1813-423T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673943 | ||||||
chr2:75674011
|
T | C | 40 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(37): Show | 61 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1813-491A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674011 | ||||||
chr2:75674034
|
AATTATAG others(9): Show |
A | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1813-530_1813-515d others(18): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674034 | ||||||
chr2:75674140
|
T | C | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1813-620A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674140 | ||||||
chr2:75674391
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1813-871A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674391 | ||||||
chr2:75674437
|
C | T | 3 | a0003c0004t0004g0277a0003c0004t0004g0284a0003c0004t0004g0285 | 3 | HG02615.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1813-917G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674437 | ||||||
chr2:75674502
|
GA | G | 3 | a0003c0004t0004g0022a0003c0004t0004g0279a0003c0004t0004g0281 | 5 | HG02451.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1813-983delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674502 | ||||||
chr2:75674505
|
A | G | 3 | a0003c0004t0004g0022a0003c0004t0004g0279a0003c0004t0004g0281 | 5 | HG02451.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1813-985T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674505 | ||||||
chr2:75674542
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(267): Show | 373 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.1813-1022T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674542 | ||||||
chr2:75674562
|
G | A | 2 | a0002c0002t0002g0128a0002c0002t0002g0148 | 2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1813-1042C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674562 | ||||||
chr2:75674588
|
T | C | 5 | a0002c0002t0009g0046a0002c0002t0009g0296a0006c0009t0005g0278others(2): Show | 6 | HG02622.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1813-1068A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674588 | ||||||
chr2:75674601
|
T | G | 1 | a0002c0002t0014g0138 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1813-1081A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674601 | ||||||
chr2:75674678
|
A | T | 105 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(102): Show | 147 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.1813-1158T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674678 | ||||||
chr2:75674699
|
T | C | 1 | a0002c0002t0003g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1813-1179A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674699 | ||||||
chr2:75674720
|
T | C | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1813-1200A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674720 | ||||||
chr2:75674756
|
T | C | 1 | a0003c0004t0005g0024 | 3 | HG03195.hp2 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1813-1236A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674756 | ||||||
chr2:75675153
|
G | A | 2 | a0013c0014t0007g0160a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1813-1633C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675153 | ||||||
chr2:75675254
|
C | T | 42 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1813-1734G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675254 | ||||||
chr2:75675315
|
T | G | 1 | a0001c0001t0001g0075 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1813-1795A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675315 | ||||||
chr2:75675379
|
ATAC | A | 67 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(64): Show | 99 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(96): Show |
intron_variant | MODIFIER | c.1813-1862_1813-186 others(7): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675379 | ||||||
chr2:75675465
|
G | A | 1 | a0002c0002t0002g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1813-1945C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675465 | ||||||
chr2:75675519
|
G | T | 3 | a0006c0009t0005g0278a0006c0009t0005g0289a0015c0015t0007g0158 | 3 | HG02976.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1813-1999C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675519 | ||||||
chr2:75675576
|
C | T | 2 | a0013c0014t0007g0160a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1813-2056G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675576 | ||||||
chr2:75675741
|
C | A | 2 | a0004c0003t0018g0071a0009c0011t0007g0052 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1813-2221G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | ||||||
chr2:75675741
|
C | CA | 20 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0171others(17): Show | 21 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1813-2222dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | ||||||
chr2:75675741
|
C | CAA | 60 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(57): Show | 90 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1813-2223_1813-222 others(6): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | ||||||
chr2:75675741
|
C | CAAA | 16 | a0002c0002t0003g0099a0002c0002t0003g0112a0002c0002t0003g0118others(13): Show | 20 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1813-2224_1813-222 others(7): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | ||||||
chr2:75675741
|
CA | C | 7 | a0001c0001t0001g0184a0001c0001t0001g0186a0002c0002t0009g0046others(4): Show | 8 | HG00597.hp1 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1813-2222delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | ||||||
chr2:75675743
|
A | C | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1813-2223T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675743 | ||||||
chr2:75675755
|
AAAAC | A | 17 | a0004c0003t0004g0003a0004c0003t0004g0025a0004c0003t0004g0059others(14): Show | 24 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1813-2239_1813-223 others(8): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675755 | ||||||
chr2:75676044
|
A | G | 149 | a0001c0001t0001g0216a0001c0001t0002g0214a0002c0002t0002g0002others(146): Show | 206 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.1813-2524T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676044 | ||||||
chr2:75676289
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1813-2769G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676289 | ||||||
chr2:75676399
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1813-2879T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676399 | ||||||
chr2:75676410
|
T | C | 18 | a0004c0003t0004g0003a0004c0003t0004g0025a0004c0003t0004g0058others(15): Show | 25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1813-2890A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676410 | ||||||
chr2:75676466
|
C | CT | 9 | a0001c0001t0001g0038a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 10 | HG02155.hp1 HG02258.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.1813-2947dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676466 | ||||||
chr2:75676466
|
CT | C | 50 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(47): Show | 68 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1813-2947delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676466 | ||||||
chr2:75676484
|
C | G | 1 | a0002c0002t0002g0164 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1813-2964G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676484 | ||||||
chr2:75676535
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1813-3015G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676535 | ||||||
chr2:75676718
|
G | A | 2 | a0004c0003t0018g0071a0009c0011t0007g0052 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1813-3198C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676718 | ||||||
chr2:75676738
|
T | C | 148 | a0001c0001t0002g0214a0002c0002t0002g0002a0002c0002t0002g0006others(145): Show | 205 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.1813-3218A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676738 | ||||||
chr2:75676810
|
G | C | 2 | a0013c0014t0007g0160a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1813-3290C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676810 | ||||||
chr2:75676973
|
G | A | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1812+3220C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676973 | ||||||
chr2:75676976
|
G | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1812+3217C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676976 | ||||||
chr2:75677086
|
A | G | 1 | a0017c0022t0016g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1812+3107T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677086 | ||||||
chr2:75677484
|
G | A | 51 | a0003c0004t0002g0286a0003c0004t0004g0022a0003c0004t0004g0044others(48): Show | 71 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.1812+2709C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677484 | ||||||
chr2:75677775
|
A | G | 20 | a0001c0001t0001g0081a0002c0002t0003g0030a0004c0003t0004g0003others(17): Show | 28 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1812+2418T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677775 | ||||||
chr2:75677777
|
T | G | 20 | a0001c0001t0001g0081a0002c0002t0003g0030a0004c0003t0004g0003others(17): Show | 28 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1812+2416A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677777 | ||||||
chr2:75677805
|
C | T | 1 | a0013c0014t0007g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1812+2388G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677805 | ||||||
chr2:75677806
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1812+2387C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677806 | ||||||
chr2:75677832
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1812+2361C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677832 | ||||||
chr2:75677870
|
C | G | 18 | a0004c0003t0004g0003a0004c0003t0004g0025a0004c0003t0004g0058others(15): Show | 25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1812+2323G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677870 | ||||||
chr2:75678015
|
A | C | 1 | a0002c0002t0003g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1812+2178T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678015 | ||||||
chr2:75678018
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0249 | 2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1812+2175C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678018 | ||||||
chr2:75678048
|
A | AGGT | 39 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(36): Show | 60 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1812+2142_1812+214 others(7): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678048 | ||||||
chr2:75678048
|
A | T | 1 | a0002c0002t0003g0099 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1812+2145T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678048 | ||||||
chr2:75678143
|
C | T | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1812+2050G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678143 | ||||||
chr2:75678153
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1812+2040A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678153 | ||||||
chr2:75678240
|
T | C | 2 | a0013c0014t0007g0160a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1812+1953A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678240 | ||||||
chr2:75678403
|
G | A | 1 | a0003c0004t0004g0285 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1812+1790C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678403 | ||||||
chr2:75678593
|
C | T | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1812+1600G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678593 | ||||||
chr2:75678822
|
A | G | 1 | a0001c0016t0001g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1812+1371T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678822 | ||||||
chr2:75679020
|
G | T | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1812+1173C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679020 | ||||||
chr2:75679085
|
GTGTT | G | 94 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(91): Show | 135 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(132): Show |
intron_variant | MODIFIER | c.1812+1104_1812+110 others(8): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679085 | ||||||
chr2:75679331
|
C | T | 1 | a0002c0005t0005g0225 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1812+862G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679331 | ||||||
chr2:75679498
|
C | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(227): Show | 321 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.1812+695G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679498 | ||||||
chr2:75679793
|
A | AT | 42 | a0001c0016t0001g0173a0002c0002t0003g0005a0002c0002t0003g0007others(39): Show | 63 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.1812+399dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679793 | ||||||
chr2:75679846
|
G | A | 42 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1812+347C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679846 | ||||||
chr2:75679868
|
T | G | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1812+325A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679868 | ||||||
chr2:75679935
|
T | A | 1 | a0003c0004t0004g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1812+258A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679935 | ||||||
chr2:75680010
|
AT | A | 42 | a0001c0016t0001g0173a0002c0002t0003g0005a0002c0002t0003g0007others(39): Show | 63 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.1812+182delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75680010 | ||||||
chr2:75680079
|
C | T | 4 | a0002c0002t0003g0027a0002c0002t0003g0098a0002c0002t0003g0107others(1): Show | 5 | HG00735.hp1 HG01069.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1812+114G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75680079 | ||||||
chr2:75680091
|
T | C | 1 | a0004c0003t0004g0062 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1812+102A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75680091 | ||||||
chr2:75680172
|
C | A | 1 | a0001c0001t0001g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1812+21G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75680172 | ||||||
chr2:75680862
|
A | G | 1 | a0002c0002t0022g0145 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1691-548T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75680862 | ||||||
chr2:75681180
|
C | T | 1 | a0002c0002t0002g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1691-866G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681180 | ||||||
chr2:75681252
|
T | C | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1691-938A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681252 | ||||||
chr2:75681314
|
GGAAGCAC others(2198): Show |
G | 2 | a0004c0003t0002g0053a0004c0003t0002g0069 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1691-3205_1691-100 others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681314 | ||||||
chr2:75681339
|
T | C | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1691-1025A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681339 | ||||||
chr2:75681370
|
C | T | 2 | a0014c0019t0001g0268a0015c0015t0007g0158 | 2 | HG02293.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1691-1056G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681370 | ||||||
chr2:75681394
|
C | G | 1 | a0002c0002t0002g0153 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1691-1080G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681394 | ||||||
chr2:75681420
|
G | A | 1 | a0018c0021t0007g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1691-1106C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681420 | ||||||
chr2:75681433
|
G | A | 1 | a0006c0009t0005g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1691-1119C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681433 | ||||||
chr2:75681433
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1691-1119C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681433 | ||||||
chr2:75681501
|
G | A | 1 | a0017c0022t0016g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1691-1187C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681501 | ||||||
chr2:75681758
|
C | T | 1 | a0002c0002t0009g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1691-1444G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681758 | ||||||
chr2:75681795
|
G | A | 24 | a0003c0004t0004g0022a0003c0004t0004g0044a0003c0004t0004g0045others(21): Show | 33 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1691-1481C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681795 | ||||||
chr2:75681826
|
C | T | 6 | a0004c0003t0004g0058a0004c0003t0004g0059a0004c0003t0004g0063others(3): Show | 6 | NA18949.hp2 NA18970.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1691-1512G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681826 | ||||||
chr2:75681835
|
C | T | 3 | a0002c0002t0003g0009a0002c0002t0003g0102a0010c0027t0003g0272 | 6 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1691-1521G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681835 | ||||||
chr2:75682106
|
C | G | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1691-1792G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682106 | ||||||
chr2:75682157
|
C | G | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1691-1843G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682157 | ||||||
chr2:75682281
|
C | T | 8 | a0003c0004t0005g0023a0003c0004t0005g0024a0003c0004t0005g0290others(5): Show | 12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1691-1967G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682281 | ||||||
chr2:75682390
|
A | T | 1 | a0001c0001t0006g0049 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1691-2076T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682390 | ||||||
chr2:75682655
|
AG | A | 3 | a0003c0004t0004g0277a0003c0004t0004g0284a0003c0004t0004g0285 | 3 | HG02615.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1691-2342delC | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682655 | ||||||
chr2:75682998
|
G | T | 1 | a0002c0002t0002g0162 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1691-2684C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682998 | ||||||
chr2:75683029
|
T | G | 2 | a0003c0004t0004g0044a0003c0004t0004g0287 | 3 | HG02922.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1691-2715A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683029 | ||||||
chr2:75683081
|
G | A | 1 | a0002c0002t0002g0150 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1691-2767C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683081 | ||||||
chr2:75683239
|
G | A | 1 | a0004c0003t0018g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1691-2925C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683239 | ||||||
chr2:75683381
|
G | A | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1691-3067C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683381 | ||||||
chr2:75683384
|
A | T | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1691-3070T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683384 | ||||||
chr2:75683530
|
C | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1691-3216G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683530 | ||||||
chr2:75683666
|
C | G | 1 | a0002c0002t0003g0112 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1691-3352G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683666 | ||||||
chr2:75683690
|
C | T | 1 | a0017c0022t0016g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1691-3376G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683690 | ||||||
chr2:75683771
|
C | CA | 37 | a0001c0001t0001g0012a0001c0001t0001g0189a0001c0001t0001g0220others(34): Show | 51 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(48): Show |
intron_variant | MODIFIER | c.1691-3458dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683771 | ||||||
chr2:75683771
|
CA | C | 23 | a0001c0001t0001g0262a0002c0002t0003g0101a0002c0002t0003g0110others(20): Show | 30 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1691-3458delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683771 | ||||||
chr2:75683786
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1691-3472T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683786 | ||||||
chr2:75683920
|
C | G | 42 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1691-3606G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683920 | ||||||
chr2:75683941
|
G | A | 2 | a0004c0003t0026g0055a0006c0009t0005g0278 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1691-3627C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683941 | ||||||
chr2:75684050
|
G | A | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1691-3736C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684050 | ||||||
chr2:75684141
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1690+3686A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684141 | ||||||
chr2:75684142
|
A | G | 1 | a0002c0002t0003g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1690+3685T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684142 | ||||||
chr2:75684229
|
G | A | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1690+3598C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684229 | ||||||
chr2:75684259
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(267): Show | 373 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.1690+3568A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684259 | ||||||
chr2:75684380
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1690+3447G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684380 | ||||||
chr2:75684447
|
C | G | 1 | a0002c0002t0003g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1690+3380G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684447 | ||||||
chr2:75684523
|
G | A | 2 | a0002c0005t0001g0234a0002c0005t0001g0235 | 2 | NA19005.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1690+3304C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684523 | ||||||
chr2:75684645
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1690+3182C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684645 | ||||||
chr2:75684651
|
T | C | 1 | a0001c0001t0001g0041 | 2 | NA18945.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1690+3176A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684651 | ||||||
chr2:75684724
|
T | C | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1690+3103A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684724 | ||||||
chr2:75684766
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1690+3061A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684766 | ||||||
chr2:75684851
|
G | A | 143 | a0001c0016t0001g0173a0002c0002t0002g0002a0002c0002t0002g0006others(140): Show | 200 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.1690+2976C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684851 | ||||||
chr2:75684859
|
T | C | 143 | a0001c0016t0001g0173a0002c0002t0002g0002a0002c0002t0002g0006others(140): Show | 200 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.1690+2968A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684859 | ||||||
chr2:75684955
|
C | T | 1 | a0007c0007t0004g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1690+2872G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684955 | ||||||
chr2:75685063
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0188 | 2 | NA18955.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1690+2764C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685063 | ||||||
chr2:75685237
|
C | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1690+2590G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685237 | ||||||
chr2:75685358
|
A | G | 1 | a0006c0009t0004g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1690+2469T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685358 | ||||||
chr2:75685482
|
T | C | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1690+2345A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685482 | ||||||
chr2:75685686
|
C | T | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1690+2141G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685686 | ||||||
chr2:75685732
|
T | C | 41 | a0001c0016t0001g0173a0002c0002t0003g0005a0002c0002t0003g0007others(38): Show | 62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1690+2095A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685732 | ||||||
chr2:75685753
|
CCTTTAAG others(5): Show |
C | 54 | a0003c0004t0002g0286a0003c0004t0004g0022a0003c0004t0004g0044others(51): Show | 74 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.1690+2062_1690+207 others(16): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685753 | ||||||
chr2:75685766
|
T | A | 54 | a0003c0004t0002g0286a0003c0004t0004g0022a0003c0004t0004g0044others(51): Show | 74 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.1690+2061A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685766 | ||||||
chr2:75685769
|
A | G | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1690+2058T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685769 | ||||||
chr2:75685844
|
T | C | 2 | a0002c0002t0003g0117a0002c0002t0003g0118 | 2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1690+1983A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685844 | ||||||
chr2:75685978
|
T | C | 1 | a0002c0002t0003g0119 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1690+1849A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685978 | ||||||
chr2:75686165
|
T | C | 1 | a0006c0009t0004g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1690+1662A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686165 | ||||||
chr2:75686170
|
T | G | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1690+1657A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686170 | ||||||
chr2:75686206
|
A | T | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1690+1621T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686206 | ||||||
chr2:75686345
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(238): Show | 332 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.1690+1482A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686345 | ||||||
chr2:75686347
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(238): Show | 332 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.1690+1480A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686347 | ||||||
chr2:75686348
|
G | A | 1 | a0002c0002t0003g0103 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1690+1479C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686348 | ||||||
chr2:75686391
|
C | G | 148 | a0001c0016t0001g0173a0002c0002t0002g0002a0002c0002t0002g0006others(145): Show | 205 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.1690+1436G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686391 | ||||||
chr2:75686469
|
A | G | 48 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(45): Show | 65 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1690+1358T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686469 | ||||||
chr2:75686515
|
A | T | 18 | a0004c0003t0004g0003a0004c0003t0004g0025a0004c0003t0004g0058others(15): Show | 25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+1312T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686515 | ||||||
chr2:75686615
|
G | A | 1 | a0002c0002t0003g0005 | 6 | NA18947.hp1 NA18979.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1690+1212C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686615 | ||||||
chr2:75686703
|
C | T | 2 | a0003c0004t0004g0284a0003c0004t0004g0285 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1690+1124G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686703 | ||||||
chr2:75686723
|
G | A | 1 | a0002c0002t0002g0142 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1690+1104C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686723 | ||||||
chr2:75686775
|
T | A | 8 | a0003c0004t0005g0023a0003c0004t0005g0024a0003c0004t0005g0290others(5): Show | 12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1690+1052A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686775 | ||||||
chr2:75686780
|
C | T | 1 | a0002c0002t0014g0138 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1690+1047G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686780 | ||||||
chr2:75686898
|
C | T | 1 | a0017c0022t0016g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1690+929G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686898 | ||||||
chr2:75686918
|
A | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(69): Show | 103 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1690+909T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686918 | ||||||
chr2:75686937
|
A | AT | 145 | a0001c0001t0001g0198a0001c0016t0001g0173a0002c0002t0002g0002others(142): Show | 202 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.1690+889dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686937 | ||||||
chr2:75686956
|
C | T | 1 | a0001c0025t0001g0264 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1690+871G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686956 | ||||||
chr2:75687004
|
G | A | 42 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1690+823C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687004 | ||||||
chr2:75687010
|
C | T | 41 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(38): Show | 56 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1690+817G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687010 | ||||||
chr2:75687011
|
C | T | 1 | a0006c0009t0004g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1690+816G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687011 | ||||||
chr2:75687036
|
G | A | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1690+791C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687036 | ||||||
chr2:75687037
|
C | A | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1690+790G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687037 | ||||||
chr2:75687067
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1690+760A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687067 | ||||||
chr2:75687069
|
G | C | 1 | a0001c0001t0006g0051 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1690+758C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687069 | ||||||
chr2:75687248
|
T | A | 24 | a0003c0004t0004g0022a0003c0004t0004g0044a0003c0004t0004g0045others(21): Show | 33 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1690+579A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687248 | ||||||
chr2:75687250
|
A | T | 1 | a0002c0002t0003g0104 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1690+577T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687250 | ||||||
chr2:75687310
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1690+517A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687310 | ||||||
chr2:75687514
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1690+313C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687514 | ||||||
chr2:75687573
|
C | G | 1 | a0004c0003t0004g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1690+254G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687573 | ||||||
chr2:75687589
|
T | A | 3 | a0004c0003t0004g0058a0004c0003t0004g0059a0004c0003t0004g0067 | 3 | NA18949.hp2 NA18970.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1690+238A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687589 | ||||||
chr2:75687684
|
T | G | 1 | a0002c0002t0003g0104 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1690+143A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687684 | ||||||
chr2:75687743
|
A | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0198a0001c0001t0011g0197others(1): Show | 4 | HG02451.hp1 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+84T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687743 | ||||||
chr2:75687749
|
G | T | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1690+78C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687749 | ||||||
chr2:75688126
|
G | A | 1 | a0002c0002t0002g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1540-149C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688126 | ||||||
chr2:75688243
|
G | A | 41 | a0001c0016t0001g0173a0002c0002t0003g0005a0002c0002t0003g0007others(38): Show | 62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1540-266C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688243 | ||||||
chr2:75688244
|
C | A | 24 | a0003c0004t0004g0022a0003c0004t0004g0044a0003c0004t0004g0045others(21): Show | 33 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1540-267G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688244 | ||||||
chr2:75688255
|
T | C | 1 | a0017c0022t0016g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1540-278A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688255 | ||||||
chr2:75688323
|
T | C | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1540-346A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688323 | ||||||
chr2:75688335
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1540-358T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688335 | ||||||
chr2:75688466
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1540-489A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688466 | ||||||
chr2:75688605
|
C | T | 5 | a0001c0001t0001g0168a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+421G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688605 | ||||||
chr2:75688729
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1539+297G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688729 | ||||||
chr2:75688794
|
TA | T | 42 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1539+231delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688794 | ||||||
chr2:75688796
|
A | T | 1 | a0002c0002t0003g0104 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1539+230T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688796 | ||||||
chr2:75688963
|
T | C | 1 | a0002c0005t0001g0177 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1539+63A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688963 | ||||||
chr2:75688968
|
A | C | 2 | a0004c0003t0002g0053a0004c0003t0002g0069 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1539+58T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688968 | ||||||
chr2:75689247
|
TTATGCAT others(12): Show |
T | 1 | a0002c0002t0003g0104 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1340-41_1340-23del others(19): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689247 | ||||||
chr2:75689254
|
T | A | 1 | a0001c0001t0013g0026 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1340-29A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689254 | ||||||
chr2:75689308
|
G | A | 1 | a0002c0002t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1340-83C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689308 | ||||||
chr2:75689452
|
C | T | 2 | a0017c0022t0016g0159a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1340-227G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689452 | ||||||
chr2:75689457
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1340-232C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689457 | ||||||
chr2:75689799
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0205a0001c0001t0001g0253others(2): Show | 8 | HG01192.hp1 HG01346.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339+170G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689799 | ||||||
chr2:75689862
|
C | A | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1339+107G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689862 | ||||||
chr2:75690159
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1227-78G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 8/16 | chr2 | 75690159 | ||||||
chr2:75690361
|
A | G | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1226+277T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 8/16 | chr2 | 75690361 | ||||||
chr2:75690401
|
A | G | 1 | a0004c0003t0004g0063 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1226+237T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 8/16 | chr2 | 75690401 | ||||||
chr2:75690486
|
G | A | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1226+152C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 8/16 | chr2 | 75690486 | ||||||
chr2:75690763
|
G | T | 41 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(38): Show | 62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1145-44C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75690763 | ||||||
chr2:75690846
|
A | G | 1 | a0006c0009t0005g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1145-127T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75690846 | ||||||
chr2:75690944
|
T | G | 66 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(63): Show | 90 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1145-225A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75690944 | ||||||
chr2:75690960
|
T | C | 15 | a0004c0003t0004g0003a0004c0003t0004g0025a0004c0003t0004g0058others(12): Show | 22 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1145-241A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75690960 | ||||||
chr2:75691200
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1145-481A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691200 | ||||||
chr2:75691306
|
T | C | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1145-587A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691306 | ||||||
chr2:75691416
|
C | T | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1144+561G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691416 | ||||||
chr2:75691445
|
G | C | 2 | a0002c0002t0002g0034a0002c0002t0002g0149 | 3 | HG00323.hp2 HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1144+532C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691445 | ||||||
chr2:75691522
|
T | C | 41 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(38): Show | 62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1144+455A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691522 | ||||||
chr2:75691757
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1144+220A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691757 | ||||||
chr2:75691860
|
T | TAA | 41 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(38): Show | 56 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1144+115_1144+116d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691860 | ||||||
chr2:75692146
|
A | AAT | 23 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0077others(20): Show | 33 | HG00140.hp1 HG00609.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.1021-48_1021-47dup others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692146 | ||||||
chr2:75692146
|
AAT | A | 8 | a0001c0001t0001g0086a0001c0001t0001g0217a0001c0001t0001g0226others(5): Show | 8 | HG00621.hp2 HG01099.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-48_1021-47del others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692146 | ||||||
chr2:75692146
|
AATAT | A | 140 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(137): Show | 196 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.1021-50_1021-47del others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692146 | ||||||
chr2:75692146
|
AATATATA others(1): Show |
A | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1021-54_1021-47del others(8): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692146 | ||||||
chr2:75692166
|
T | C | 41 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(38): Show | 56 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1021-66A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692166 | ||||||
chr2:75692168
|
T | C | 143 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(140): Show | 199 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.1021-68A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692168 | ||||||
chr2:75692170
|
T | C | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1021-70A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692170 | ||||||
chr2:75692171
|
A | G | 1 | a0006c0009t0004g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1021-71T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692171 | ||||||
chr2:75692228
|
A | G | 1 | a0013c0014t0007g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1021-128T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692228 | ||||||
chr2:75692353
|
T | C | 3 | a0002c0002t0003g0131a0013c0014t0007g0160a0018c0021t0007g0161 | 3 | HG00735.hp1 HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1021-253A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692353 | ||||||
chr2:75692361
|
C | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1021-261G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692361 | ||||||
chr2:75692374
|
AG | A | 144 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(141): Show | 201 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.1021-275delC | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692374 | ||||||
chr2:75692522
|
C | G | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1021-422G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692522 | ||||||
chr2:75692827
|
G | A | 1 | a0002c0005t0005g0225 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1021-727C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692827 | ||||||
chr2:75692879
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0258 | 2 | NA18972.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1021-779G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692879 | ||||||
chr2:75692891
|
T | G | 1 | a0001c0001t0001g0262 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1021-791A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692891 | ||||||
chr2:75692900
|
T | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0208a0001c0001t0001g0210others(3): Show | 8 | HG00609.hp1 HG01934.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021-800A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692900 | ||||||
chr2:75693355
|
G | A | 1 | a0003c0004t0002g0286 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1020+886C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693355 | ||||||
chr2:75693400
|
A | G | 1 | a0004c0003t0004g0062 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1020+841T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693400 | ||||||
chr2:75693426
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1020+815G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693426 | ||||||
chr2:75693525
|
A | C | 1 | a0002c0002t0002g0144 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1020+716T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693525 | ||||||
chr2:75693640
|
T | G | 2 | a0013c0014t0007g0160a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1020+601A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693640 | ||||||
chr2:75693735
|
A | G | 1 | a0002c0002t0003g0005 | 6 | NA18947.hp1 NA18979.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+506T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693735 | ||||||
chr2:75693993
|
T | A | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1020+248A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693993 | ||||||
chr2:75694106
|
G | GCTTA | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1020+134_1020+135i others(6): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75694106 | ||||||
chr2:75694133
|
G | C | 1 | a0001c0001t0001g0253 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1020+108C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75694133 | ||||||
chr2:75694553
|
T | C | 1 | a0004c0003t0004g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.834-126A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75694553 | ||||||
chr2:75694841
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0189 | 4 | NA18949.hp1 NA18953.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.834-414C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75694841 | ||||||
chr2:75694997
|
TGA | T | 2 | a0002c0002t0003g0009a0010c0027t0003g0272 | 5 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.834-572_834-571del others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75694997 | ||||||
chr2:75695083
|
C | T | 3 | a0004c0003t0004g0058a0004c0003t0004g0059a0004c0003t0004g0067 | 3 | NA18949.hp2 NA18970.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.834-656G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695083 | ||||||
chr2:75695124
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.834-697G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695124 | ||||||
chr2:75695167
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.834-740G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695167 | ||||||
chr2:75695196
|
T | C | 2 | a0004c0003t0018g0071a0009c0011t0007g0052 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.834-769A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695196 | ||||||
chr2:75695314
|
ATCCAG | A | 3 | a0006c0009t0004g0273a0006c0009t0004g0274a0015c0015t0007g0158 | 3 | HG02818.hp2 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.833+881_833+885del others(5): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695314 | ||||||
chr2:75695485
|
T | C | 15 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0182others(12): Show | 18 | HG00423.hp1 HG00609.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.833+715A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695485 | ||||||
chr2:75695522
|
C | T | 2 | a0001c0001t0001g0211a0002c0002t0017g0137 | 2 | HG02129.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.833+678G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695522 | ||||||
chr2:75695556
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0198 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.833+644G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695556 | ||||||
chr2:75695714
|
T | C | 1 | a0002c0002t0002g0128 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.833+486A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695714 | ||||||
chr2:75695901
|
G | A | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.833+299C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695901 | ||||||
chr2:75695926
|
G | T | 2 | a0006c0009t0004g0273a0006c0009t0004g0274 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.833+274C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695926 | ||||||
chr2:75695982
|
C | T | 1 | a0002c0002t0003g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.833+218G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695982 | ||||||
chr2:75696172
|
T | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0261 | 3 | HG03491.hp2 HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.833+28A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75696172 | ||||||
chr2:75696430
|
T | C | 1 | a0002c0005t0001g0177 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.718-115A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696430 | ||||||
chr2:75696600
|
G | C | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.718-285C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696600 | ||||||
chr2:75696606
|
T | A | 24 | a0003c0004t0004g0022a0003c0004t0004g0044a0003c0004t0004g0045others(21): Show | 33 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.718-291A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696606 | ||||||
chr2:75696694
|
C | A | 1 | a0004c0003t0018g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.718-379G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696694 | ||||||
chr2:75696696
|
T | A | 1 | a0017c0022t0016g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.718-381A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696696 | ||||||
chr2:75696778
|
T | C | 1 | a0002c0002t0002g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.718-463A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696778 | ||||||
chr2:75696849
|
A | C | 7 | a0003c0004t0002g0286a0004c0003t0002g0013a0004c0003t0002g0053others(4): Show | 9 | HG00735.hp2 HG02055.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-534T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696849 | ||||||
chr2:75696886
|
C | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.718-571G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696886 | ||||||
chr2:75697496
|
C | T | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.718-1181G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697496 | ||||||
chr2:75697534
|
A | T | 1 | a0002c0002t0002g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.718-1219T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697534 | ||||||
chr2:75697624
|
C | T | 1 | a0006c0009t0005g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.718-1309G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697624 | ||||||
chr2:75697690
|
A | G | 19 | a0002c0005t0001g0021a0002c0005t0001g0035a0002c0005t0001g0165others(16): Show | 22 | HG00408.hp1 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.718-1375T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697690 | ||||||
chr2:75697726
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.718-1411G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697726 | ||||||
chr2:75697739
|
G | A | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.718-1424C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697739 | ||||||
chr2:75697787
|
T | G | 53 | a0003c0004t0002g0286a0003c0004t0004g0022a0003c0004t0004g0044others(50): Show | 73 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.718-1472A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697787 | ||||||
chr2:75698407
|
G | C | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.718-2092C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698407 | ||||||
chr2:75698508
|
G | T | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.718-2193C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698508 | ||||||
chr2:75698518
|
CAA | C | 2 | a0003c0004t0004g0044a0003c0004t0004g0287 | 3 | HG02922.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.718-2205_718-2204d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698518 | ||||||
chr2:75698619
|
T | G | 1 | a0002c0002t0002g0127 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.718-2304A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698619 | ||||||
chr2:75698871
|
G | C | 1 | a0006c0009t0005g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.717+2319C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698871 | ||||||
chr2:75698887
|
G | A | 7 | a0003c0004t0002g0286a0004c0003t0002g0013a0004c0003t0002g0053others(4): Show | 9 | HG00735.hp2 HG02055.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.717+2303C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698887 | ||||||
chr2:75698991
|
G | A | 18 | a0002c0005t0001g0021a0002c0005t0001g0035a0002c0005t0001g0165others(15): Show | 21 | HG00408.hp1 HG00738.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.717+2199C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698991 | ||||||
chr2:75699011
|
C | CA | 43 | a0001c0001t0001g0255a0002c0002t0003g0005a0002c0002t0003g0007others(40): Show | 65 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.717+2178dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699011 | ||||||
chr2:75699032
|
T | C | 1 | a0006c0009t0004g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.717+2158A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699032 | ||||||
chr2:75699112
|
G | C | 95 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(92): Show | 136 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.717+2078C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699112 | ||||||
chr2:75699118
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.717+2072G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699118 | ||||||
chr2:75699417
|
G | A | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.717+1773C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699417 | ||||||
chr2:75699439
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(69): Show | 103 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.717+1751A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699439 | ||||||
chr2:75699562
|
A | ATATT | 5 | a0003c0004t0005g0024a0003c0004t0005g0291a0003c0004t0005g0293others(2): Show | 7 | HG01891.hp2 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1627_717+1628i others(6): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699562 | ||||||
chr2:75699563
|
C | T | 21 | a0003c0004t0004g0022a0003c0004t0004g0044a0003c0004t0004g0045others(18): Show | 28 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.717+1627G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699563 | ||||||
chr2:75699608
|
ACT | A | 3 | a0006c0009t0004g0273a0006c0009t0004g0274a0015c0015t0007g0158 | 3 | HG02818.hp2 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.717+1580_717+1581d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699608 | ||||||
chr2:75699710
|
G | C | 5 | a0003c0004t0005g0024a0003c0004t0005g0291a0003c0004t0005g0293others(2): Show | 7 | HG01891.hp2 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1480C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699710 | ||||||
chr2:75699724
|
C | T | 1 | a0003c0004t0004g0282 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.717+1466G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699724 | ||||||
chr2:75699746
|
T | C | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.717+1444A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699746 | ||||||
chr2:75699805
|
G | C | 1 | a0004c0003t0004g0065 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.717+1385C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699805 | ||||||
chr2:75699807
|
G | C | 3 | a0004c0003t0018g0071a0007c0007t0004g0014a0007c0007t0004g0070 | 5 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+1383C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699807 | ||||||
chr2:75699896
|
G | GT | 11 | a0001c0001t0001g0239a0002c0002t0002g0124a0002c0002t0002g0135others(8): Show | 12 | HG01891.hp1 HG02015.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.717+1293dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699896 | ||||||
chr2:75700027
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.717+1163T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700027 | ||||||
chr2:75700027
|
A | T | 10 | a0002c0002t0003g0009a0002c0002t0003g0017a0002c0002t0003g0095others(7): Show | 15 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(12): Show |
intron_variant | MODIFIER | c.717+1163T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700027 | ||||||
chr2:75700219
|
C | T | 1 | a0006c0009t0005g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+971G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700219 | ||||||
chr2:75700306
|
A | G | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.717+884T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700306 | ||||||
chr2:75700391
|
C | A | 29 | a0003c0004t0002g0286a0004c0003t0002g0013a0004c0003t0002g0053others(26): Show | 40 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.717+799G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700391 | ||||||
chr2:75700393
|
CATA | C | 3 | a0003c0004t0004g0277a0003c0004t0004g0284a0003c0004t0004g0285 | 3 | HG02615.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.717+794_717+796del others(3): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700393 | ||||||
chr2:75700410
|
T | C | 42 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.717+780A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700410 | ||||||
chr2:75700509
|
G | A | 41 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0009others(38): Show | 62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.717+681C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700509 | ||||||
chr2:75700514
|
G | T | 1 | a0001c0001t0011g0197 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.717+676C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700514 | ||||||
chr2:75700524
|
C | A | 2 | a0007c0007t0004g0014a0007c0007t0004g0070 | 4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+666G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700524 | ||||||
chr2:75700572
|
G | A | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.717+618C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700572 | ||||||
chr2:75700632
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.717+558A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700632 | ||||||
chr2:75700757
|
T | C | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.717+433A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700757 | ||||||
chr2:75700780
|
T | C | 18 | a0004c0003t0004g0003a0004c0003t0004g0025a0004c0003t0004g0058others(15): Show | 25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.717+410A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700780 | ||||||
chr2:75700846
|
T | C | 3 | a0004c0003t0004g0072a0004c0003t0004g0073a0004c0003t0004g0074 | 3 | HG02809.hp1 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.717+344A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700846 | ||||||
chr2:75700980
|
C | T | 1 | a0006c0009t0005g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.717+210G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700980 | ||||||
chr2:75700996
|
G | C | 20 | a0002c0002t0002g0002a0002c0002t0002g0032a0002c0002t0002g0033others(17): Show | 30 | HG00323.hp2 HG00639.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.717+194C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700996 | ||||||
chr2:75701107
|
G | A | 2 | a0002c0005t0001g0178a0002c0005t0005g0225 | 2 | HG01257.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.717+83C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75701107 | ||||||
chr2:75701174
|
G | T | 146 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(143): Show | 203 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.717+16C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75701174 | ||||||
chr2:75701648
|
T | C | 1 | a0004c0003t0026g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.620-361A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75701648 | ||||||
chr2:75701692
|
C | T | 1 | a0006c0009t0005g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.620-405G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75701692 | ||||||
chr2:75701719
|
T | C | 1 | a0003c0004t0004g0279 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.620-432A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75701719 | ||||||
chr2:75701821
|
A | G | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.619+378T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75701821 | ||||||
chr2:75702004
|
C | A | 113 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(110): Show | 160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.619+195G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75702004 | ||||||
chr2:75702112
|
C | A | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.619+87G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75702112 | ||||||
chr2:75702196
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19080.hp1 | splice_region_variant&intron_variant | LOW | c.619+3A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75702196 | ||||||
chr2:75702539
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.395-116A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702539 | ||||||
chr2:75702645
|
A | C | 25 | a0003c0004t0002g0286a0003c0004t0004g0022a0003c0004t0004g0044others(22): Show | 34 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.395-222T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702645 | ||||||
chr2:75702682
|
C | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.395-259G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702682 | ||||||
chr2:75702760
|
G | A | 3 | a0002c0002t0002g0130a0002c0002t0002g0150a0002c0002t0002g0155 | 3 | HG02027.hp1 NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.395-337C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702760 | ||||||
chr2:75702922
|
C | G | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.395-499G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702922 | ||||||
chr2:75702969
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.395-546C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702969 | ||||||
chr2:75702979
|
T | C | 2 | a0004c0003t0018g0071a0009c0011t0007g0052 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.395-556A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702979 | ||||||
chr2:75703016
|
G | A | 1 | a0002c0002t0003g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.395-593C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703016 | ||||||
chr2:75703095
|
C | A | 30 | a0002c0002t0003g0005a0002c0002t0003g0007a0002c0002t0003g0018others(27): Show | 46 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.395-672G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703095 | ||||||
chr2:75703211
|
G | C | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.395-788C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703211 | ||||||
chr2:75703262
|
A | C | 1 | a0005c0006t0001g0085 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.395-839T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703262 | ||||||
chr2:75703464
|
T | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0258 | 2 | NA18972.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.395-1041A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703464 | ||||||
chr2:75703686
|
C | A | 1 | a0006c0009t0005g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.395-1263G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703686 | ||||||
chr2:75703854
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0180a0001c0001t0001g0226 | 6 | HG00621.hp2 HG01175.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-1431C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703854 | ||||||
chr2:75704002
|
C | T | 41 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(38): Show | 56 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.395-1579G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704002 | ||||||
chr2:75704049
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.395-1626C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704049 | ||||||
chr2:75704077
|
C | T | 1 | a0003c0004t0004g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.395-1654G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704077 | ||||||
chr2:75704080
|
G | A | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.395-1657C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704080 | ||||||
chr2:75704086
|
G | A | 27 | a0003c0004t0002g0286a0003c0004t0004g0022a0003c0004t0004g0044others(24): Show | 36 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.395-1663C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704086 | ||||||
chr2:75704223
|
T | C | 1 | a0003c0004t0005g0295 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.395-1800A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704223 | ||||||
chr2:75704231
|
T | C | 2 | a0001c0001t0001g0213a0001c0001t0002g0214 | 2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.395-1808A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704231 | ||||||
chr2:75704393
|
A | G | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.395-1970T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704393 | ||||||
chr2:75704403
|
C | T | 1 | a0016c0017t0001g0230 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.395-1980G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704403 | ||||||
chr2:75704432
|
G | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG00597.hp2 HG02155.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-2009C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704432 | ||||||
chr2:75704463
|
T | A | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.395-2040A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704463 | ||||||
chr2:75704470
|
G | A | 2 | a0001c0001t0006g0050a0001c0001t0006g0051 | 2 | NA18987.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.395-2047C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704470 | ||||||
chr2:75704474
|
T | G | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.394+2049A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704474 | ||||||
chr2:75704927
|
C | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(62): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.394+1596G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704927 | ||||||
chr2:75704936
|
A | G | 42 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.394+1587T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704936 | ||||||
chr2:75705193
|
G | A | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.394+1330C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705193 | ||||||
chr2:75705238
|
C | T | 1 | a0017c0022t0016g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394+1285G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705238 | ||||||
chr2:75705292
|
A | C | 5 | a0006c0009t0004g0273a0006c0009t0004g0274a0013c0014t0007g0160others(2): Show | 5 | HG02683.hp2 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+1231T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705292 | ||||||
chr2:75705345
|
C | T | 2 | a0006c0009t0004g0273a0006c0009t0004g0274 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.394+1178G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705345 | ||||||
chr2:75705361
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(69): Show | 103 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.394+1162G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705361 | ||||||
chr2:75705439
|
C | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0184others(5): Show | 11 | HG00597.hp1 NA18944.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.394+1084G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705439 | ||||||
chr2:75705501
|
T | C | 43 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(40): Show | 58 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.394+1022A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705501 | ||||||
chr2:75705515
|
GCTAAGGC others(62): Show |
G | 18 | a0004c0003t0004g0003a0004c0003t0004g0025a0004c0003t0004g0058others(15): Show | 25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.394+939_394+1007de others(70): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705515 | ||||||
chr2:75705616
|
C | CA | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.394+906dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | ||||||
chr2:75705616
|
C | CAA | 42 | a0001c0001t0001g0082a0001c0001t0001g0183a0001c0001t0001g0262others(39): Show | 56 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.394+905_394+906dup others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | ||||||
chr2:75705616
|
C | CAAA | 12 | a0002c0002t0002g0124a0002c0002t0002g0134a0003c0010t0004g0275others(9): Show | 13 | HG00438.hp2 HG02015.hp1 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.394+904_394+906dup others(3): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | ||||||
chr2:75705616
|
C | CAAAA | 33 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0033others(30): Show | 47 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.394+903_394+906dup others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | ||||||
chr2:75705616
|
C | CAAAAA | 8 | a0002c0002t0002g0032a0002c0002t0002g0129a0002c0002t0002g0130others(5): Show | 9 | HG00735.hp1 HG01256.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+902_394+906dup others(5): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | ||||||
chr2:75705720
|
C | T | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.394+803G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705720 | ||||||
chr2:75705815
|
C | T | 2 | a0002c0002t0002g0032a0002c0002t0002g0154 | 3 | HG01256.hp1 HG01515.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.394+708G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705815 | ||||||
chr2:75705825
|
C | T | 1 | a0006c0009t0004g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394+698G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705825 | ||||||
chr2:75705938
|
T | C | 1 | a0004c0003t0004g0074 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.394+585A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705938 | ||||||
chr2:75706004
|
G | A | 43 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(40): Show | 58 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.394+519C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706004 | ||||||
chr2:75706004
|
G | C | 1 | a0002c0005t0001g0236 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.394+519C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706004 | ||||||
chr2:75706252
|
G | A | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.394+271C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706252 | ||||||
chr2:75706252
|
G | GT | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0008g0167 | 3 | NA18969.hp2 NA19081.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.394+270dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706252 | ||||||
chr2:75706315
|
T | G | 27 | a0003c0004t0002g0286a0003c0004t0004g0022a0003c0004t0004g0044others(24): Show | 36 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.394+208A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706315 | ||||||
chr2:75706464
|
A | G | 28 | a0004c0003t0002g0013a0004c0003t0002g0053a0004c0003t0002g0054others(25): Show | 39 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.394+59T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706464 | ||||||
chr2:75706655
|
A | G | 1 | a0013c0014t0007g0160 | 1 | HG03239.hp1 | splice_region_variant&intron_variant | LOW | c.266-4T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706655 | ||||||
chr2:75706704
|
T | A | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.266-53A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706704 | ||||||
chr2:75706732
|
A | G | 4 | a0004c0003t0004g0003a0004c0003t0004g0060a0004c0003t0004g0061others(1): Show | 10 | HG00639.hp1 HG01261.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.266-81T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706732 | ||||||
chr2:75706856
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.266-205A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706856 | ||||||
chr2:75706927
|
A | G | 21 | a0003c0004t0004g0022a0003c0004t0004g0044a0003c0004t0004g0045others(18): Show | 30 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.266-276T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706927 | ||||||
chr2:75707035
|
T | C | 6 | a0004c0003t0002g0013a0004c0003t0002g0053a0004c0003t0002g0054others(3): Show | 8 | HG02055.hp2 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.266-384A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707035 | ||||||
chr2:75707050
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.266-399G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707050 | ||||||
chr2:75707229
|
C | T | 1 | a0015c0015t0007g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.266-578G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707229 | ||||||
chr2:75707295
|
G | A | 1 | a0002c0002t0020g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.266-644C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707295 | ||||||
chr2:75707357
|
T | C | 2 | a0004c0003t0018g0071a0009c0011t0007g0052 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.266-706A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707357 | ||||||
chr2:75707447
|
G | C | 1 | a0006c0009t0005g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.266-796C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707447 | ||||||
chr2:75707562
|
T | TA | 115 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(112): Show | 162 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.266-912dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707562 | ||||||
chr2:75707679
|
A | G | 2 | a0007c0007t0004g0014a0007c0007t0004g0070 | 4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-1028T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707679 | ||||||
chr2:75707742
|
T | TAACATGT others(12): Show |
42 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(39): Show | 57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.266-1092_266-1091i others(21): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707742 | ||||||
chr2:75707912
|
C | G | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.266-1261G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707912 | ||||||
chr2:75707958
|
CAT | C | 3 | a0002c0002t0003g0157a0006c0009t0004g0273a0006c0009t0004g0274 | 3 | HG02818.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.266-1309_266-1308d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707958 | ||||||
chr2:75708050
|
T | C | 7 | a0002c0005t0001g0165a0002c0005t0001g0179a0002c0005t0001g0232others(4): Show | 7 | HG00408.hp1 HG02056.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-1399A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708050 | ||||||
chr2:75708079
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0180 | 5 | HG01175.hp1 HG01433.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1428G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708079 | ||||||
chr2:75708156
|
A | G | 1 | a0002c0002t0002g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.266-1505T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708156 | ||||||
chr2:75708171
|
A | C | 1 | a0002c0002t0002g0132 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.266-1520T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708171 | ||||||
chr2:75708201
|
T | G | 2 | a0002c0002t0002g0152a0002c0002t0002g0153 | 2 | NA18939.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.266-1550A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708201 | ||||||
chr2:75708303
|
C | G | 2 | a0006c0009t0005g0278a0006c0009t0005g0289 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.266-1652G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708303 | ||||||
chr2:75708405
|
G | A | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.266-1754C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708405 | ||||||
chr2:75708463
|
C | A | 1 | a0001c0001t0001g0041 | 2 | NA18945.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.266-1812G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708463 | ||||||
chr2:75708488
|
A | T | 117 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(114): Show | 165 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.266-1837T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708488 | ||||||
chr2:75708501
|
C | CT | 57 | a0001c0001t0001g0075a0001c0001t0001g0086a0001c0001t0001g0168others(54): Show | 75 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.266-1851dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | ||||||
chr2:75708501
|
C | CTT | 16 | a0002c0002t0002g0122a0002c0002t0002g0124a0002c0002t0002g0125others(13): Show | 18 | HG00735.hp1 HG01433.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.266-1852_266-1851d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | ||||||
chr2:75708501
|
CT | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(60): Show | 99 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.266-1851delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | ||||||
chr2:75708501
|
CTT | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0267a0001c0001t0019g0265others(4): Show | 8 | HG00323.hp1 HG02055.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-1852_266-1851d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | ||||||
chr2:75708501
|
CTTTTTTT others(1): Show |
C | 33 | a0002c0002t0003g0007a0002c0002t0003g0009a0002c0002t0003g0017others(30): Show | 48 | HG00621.hp1 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.266-1858_266-1851d others(10): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | ||||||
chr2:75708501
|
CTTTTTTT others(2): Show |
C | 3 | a0002c0002t0003g0005a0002c0002t0003g0031a0002c0002t0023g0121 | 9 | HG03041.hp1 NA18947.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.266-1859_266-1851d others(11): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | ||||||
chr2:75708501
|
CTTTTTTT others(9): Show |
C | 1 | a0006c0009t0005g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.266-1866_266-1851d others(18): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | ||||||
chr2:75708604
|
C | T | 40 | a0002c0002t0002g0094a0002c0002t0003g0005a0002c0002t0003g0007others(37): Show | 61 | HG00621.hp1 HG01069.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.266-1953G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708604 | ||||||
chr2:75708760
|
C | T | 10 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(7): Show | 10 | HG00423.hp2 HG00597.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.265+1831G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708760 | ||||||
chr2:75708762
|
G | A | 2 | a0013c0014t0007g0160a0018c0021t0007g0161 | 2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.265+1829C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708762 | ||||||
chr2:75708768
|
T | C | 147 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(144): Show | 204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.265+1823A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708768 | ||||||
chr2:75708774
|
G | A | 1 | a0002c0002t0002g0162 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.265+1817C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708774 | ||||||
chr2:75708911
|
T | C | 1 | a0014c0019t0001g0268 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.265+1680A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708911 | ||||||
chr2:75708970
|
C | A | 2 | a0007c0007t0004g0014a0007c0007t0004g0070 | 4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+1621G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708970 | ||||||
chr2:75709200
|
A | T | 1 | a0002c0002t0015g0093 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.265+1391T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709200 | ||||||
chr2:75709212
|
GA | G | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.265+1378delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709212 | ||||||
chr2:75709215
|
T | G | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.265+1376A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709215 | ||||||
chr2:75709217
|
C | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.265+1374G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709217 | ||||||
chr2:75709345
|
T | G | 1 | a0002c0002t0002g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.265+1246A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709345 | ||||||
chr2:75709347
|
T | C | 27 | a0003c0004t0002g0286a0003c0004t0004g0022a0003c0004t0004g0044others(24): Show | 36 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.265+1244A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709347 | ||||||
chr2:75709501
|
G | T | 8 | a0003c0004t0005g0023a0003c0004t0005g0024a0003c0004t0005g0290others(5): Show | 12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.265+1090C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709501 | ||||||
chr2:75709526
|
G | C | 8 | a0003c0004t0005g0023a0003c0004t0005g0024a0003c0004t0005g0290others(5): Show | 12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.265+1065C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709526 | ||||||
chr2:75709563
|
A | T | 2 | a0002c0002t0009g0046a0002c0002t0009g0296 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.265+1028T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709563 | ||||||
chr2:75709621
|
C | G | 1 | a0002c0002t0002g0164 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.265+970G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709621 | ||||||
chr2:75709629
|
C | T | 1 | a0002c0005t0001g0165 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.265+962G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709629 | ||||||
chr2:75709635
|
G | A | 1 | a0002c0002t0002g0164 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.265+956C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709635 | ||||||
chr2:75709809
|
T | A | 120 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(117): Show | 168 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.265+782A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709809 | ||||||
chr2:75709850
|
C | G | 145 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0032others(142): Show | 201 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.265+741G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709850 | ||||||
chr2:75709920
|
T | C | 27 | a0003c0004t0002g0286a0003c0004t0004g0022a0003c0004t0004g0044others(24): Show | 36 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.265+671A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709920 | ||||||
chr2:75709963
|
G | A | 1 | a0020c0023t0024g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.265+628C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709963 | ||||||
chr2:75710030
|
T | C | 1 | a0004c0003t0018g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.265+561A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710030 | ||||||
chr2:75710129
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.265+462T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710129 | ||||||
chr2:75710248
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.265+343T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710248 | ||||||
chr2:75710261
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(273): Show | 379 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(376): Show |
intron_variant | MODIFIER | c.265+330A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710261 | ||||||
chr2:75710274
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.265+317A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710274 | ||||||
chr2:75710482
|
T | C | 3 | a0004c0003t0004g0072a0004c0003t0004g0073a0004c0003t0004g0074 | 3 | HG02809.hp1 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.265+109A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710482 |