Item | Value |
---|---|
geneid | 2926 |
ensemblid | ENSG00000132463.15 |
hgncid | 4610 |
symbol | GRSF1 |
name | G-rich RNA sequence binding factor 1 |
refseq_nuc | NM_002092.4 |
refseq_prot | NP_002083.4 |
ensembl_nuc | ENST00000254799.11 |
ensembl_prot | ENSP00000254799.6 |
mane_status | MANE Select |
chr | chr4 |
start | 70815783 |
end | 70839890 |
strand | - |
ver | v1.2 |
region | chr4:70815783-70839890 |
region5000 | chr4:70810783-70844890 |
regionname0 | GRSF1_chr4_70815783_70839890 |
regionname5000 | GRSF1_chr4_70810783_70844890 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 480 | 321 | 84 | 53 | 137 | 10 | 36 | 103 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0002 | 1/0 | 480 | 4 | 3 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0003 | 0/0 | 480 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0004 | 0/0 | 480 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0005 | 0/0 | 480 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1443 | 315 | 79 | 52 | 137 | 10 | 36 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
c0002 | 1/0 | 1443 | 4 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
c0003 | 0/0 | 1443 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
c0004 | 0/0 | 1443 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
c0005 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
c0006 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
c0007 | 0/0 | 1443 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
c0008 | 0/0 | 1443 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
c0009 | 0/0 | 1443 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 5167 | 168 | 31 | 43 | 65 | 7 | 21 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0002 | 0/0 | 5168 | 43 | 1 | 4 | 36 | 0 | 2 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0003 | 0/0 | 5168 | 15 | 15 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0004 | 0/0 | 5168 | 12 | 2 | 1 | 5 | 0 | 4 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0005 | 0/0 | 5167 | 12 | 0 | 0 | 12 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0006 | 0/0 | 5169 | 11 | 8 | 0 | 0 | 0 | 3 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0007 | 0/0 | 5167 | 10 | 0 | 1 | 6 | 0 | 3 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0008 | 0/0 | 5167 | 6 | 0 | 0 | 6 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0009 | 0/0 | 5168 | 6 | 6 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0010 | 0/0 | 5168 | 3 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0011 | 0/0 | 5169 | 3 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0012 | 0/0 | 5168 | 3 | 0 | 0 | 0 | 3 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0013 | 0/0 | 5167 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0014 | 0/0 | 5168 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0015 | 0/0 | 5162 | 2 | 1 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0016 | 0/0 | 5169 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0017 | 0/0 | 5168 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0018 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0019 | 0/0 | 5168 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0020 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0021 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0022 | 0/0 | 5168 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0023 | 0/0 | 5167 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0024 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0025 | 0/0 | 5167 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0026 | 0/0 | 5169 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0027 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0028 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0029 | 0/0 | 5167 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0030 | 0/0 | 5168 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0031 | 0/0 | 5168 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0032 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0033 | 0/0 | 5168 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0034 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0035 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0036 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0037 | 0/0 | 5167 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0038 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0039 | 0/0 | 5164 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0040 | 0/0 | 5169 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0041 | 1/0 | 5168 | 1 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0042 | 0/0 | 5168 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0043 | 0/0 | 5168 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
t0044 | 0/0 | 5168 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 22 | 7 | 1 | 12 | 0 | 2 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0002 | 0/0 | 15 | 0 | 3 | 11 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0003 | 0/0 | 8 | 0 | 1 | 1 | 2 | 4 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0004 | 0/0 | 6 | 2 | 2 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0007 | 0/1 | 4 | 0 | 1 | 1 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0013 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1443 | 315 | 79 | 52 | 137 | 10 | 36 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0003 | 0/0 | 1443 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0004 | 0/0 | 1443 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0005 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0009 | 0/0 | 1443 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0002c0002 | 1/0 | 1443 | 4 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0003c0006 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0004c0007 | 0/0 | 1443 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0005c0008 | 0/0 | 1443 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6609 | 162 | 28 | 41 | 64 | 7 | 21 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0002 | 0/0 | 6610 | 43 | 1 | 4 | 36 | 0 | 2 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0003 | 0/0 | 6610 | 13 | 13 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0004 | 0/0 | 6610 | 12 | 2 | 1 | 5 | 0 | 4 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0005 | 0/0 | 6609 | 12 | 0 | 0 | 12 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0006 | 0/0 | 6611 | 11 | 8 | 0 | 0 | 0 | 3 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0007 | 0/0 | 6609 | 10 | 0 | 1 | 6 | 0 | 3 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0008 | 0/0 | 6609 | 6 | 0 | 0 | 6 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0009 | 0/0 | 6610 | 6 | 6 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0011 | 0/0 | 6611 | 3 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0012 | 0/0 | 6610 | 3 | 0 | 0 | 0 | 3 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0013 | 0/0 | 6609 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0014 | 0/0 | 6610 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0015 | 0/0 | 6604 | 2 | 1 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0016 | 0/0 | 6611 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0017 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0018 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0019 | 0/0 | 6610 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0020 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0021 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0022 | 0/0 | 6610 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0023 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0024 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0025 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0026 | 0/0 | 6611 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0027 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0028 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0029 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0030 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0031 | 0/0 | 6610 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0032 | 0/0 | 6609 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0033 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0034 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0035 | 0/0 | 6609 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0036 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0037 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0038 | 0/0 | 6604 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0039 | 0/0 | 6606 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0040 | 0/0 | 6611 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0042 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0001t0044 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0003t0001 | 0/0 | 6609 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0004t0003 | 0/0 | 6610 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0005t0001 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0001c0009t0001 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0002c0002t0010 | 0/0 | 6610 | 3 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0002c0002t0041 | 1/0 | 6610 | 1 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0003c0006t0043 | 0/0 | 6610 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0004c0007t0001 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
a0005c0008t0001 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | copy fasta | chr4 | 70810783 | 70844890 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 22 | 7 | 1 | 12 | 0 | 2 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 1 | 2 | 4 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0004 | 0/0 | 6 | 2 | 2 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0007 | 0/1 | 4 | 0 | 1 | 1 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0013 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0002 | 0/0 | 15 | 0 | 3 | 11 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0006g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0007g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0008g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0009g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0009g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0011g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0012g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0012g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0014g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0015g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0015g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0016g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0017g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0018g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0019g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0020g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0021g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0022g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0023g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0024g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0025g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0026g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0027g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0028g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0029g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0030g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0031g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0032g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0033g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0034g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0035g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0036g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0037g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0038g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0039g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0040g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0042g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0001t0044g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0003t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0004t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0001c0009t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0002c0002t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0002c0002t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0002c0002t0010g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0002c0002t0041g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0003c0006t0043g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0004c0007t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
a0005c0008t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00323 | hp1 | a0001 | c0001 | t0012 | g0056 | EUR | FIN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00597 | hp1 | a0001 | c0001 | t0027 | g0168 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00609 | hp1 | a0001 | c0001 | t0008 | g0165 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00639 | hp2 | a0004 | c0007 | t0001 | g0118 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00673 | hp2 | a0001 | c0001 | t0018 | g0157 | EAS | CHS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01106 | hp1 | a0001 | c0001 | t0023 | g0096 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01167 | hp2 | a0001 | c0001 | t0015 | g0073 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01361 | hp1 | a0001 | c0001 | t0029 | g0187 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01515 | hp2 | a0001 | c0001 | t0012 | g0055 | EUR | IBS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01517 | hp1 | a0001 | c0001 | t0012 | g0054 | EUR | IBS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01884 | hp1 | a0001 | c0001 | t0017 | g0046 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01975 | hp2 | a0001 | c0009 | t0001 | g0222 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02027 | hp1 | a0001 | c0001 | t0008 | g0164 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02040 | hp1 | a0001 | c0001 | t0036 | g0053 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02056 | hp2 | a0001 | c0001 | t0008 | g0172 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02080 | hp1 | a0001 | c0001 | t0008 | g0036 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02148 | hp2 | a0001 | c0001 | t0025 | g0137 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02155 | hp2 | a0001 | c0001 | t0022 | g0202 | EAS | CDX | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02257 | hp1 | a0001 | c0001 | t0020 | g0135 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02258 | hp1 | a0001 | c0001 | t0042 | g0196 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0103 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02280 | hp2 | a0001 | c0001 | t0038 | g0075 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02300 | hp1 | a0001 | c0001 | t0037 | g0084 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02451 | hp1 | a0001 | c0001 | t0021 | g0166 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02572 | hp2 | a0001 | c0001 | t0044 | g0058 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0069 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0019 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0105 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0016 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02723 | hp1 | a0001 | c0001 | t0028 | g0175 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02723 | hp2 | a0001 | c0001 | t0039 | g0195 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0220 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0051 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0016 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02818 | hp1 | a0001 | c0001 | t0016 | g0018 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02818 | hp2 | a0001 | c0001 | t0015 | g0074 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02886 | hp2 | a0001 | c0001 | t0014 | g0042 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02922 | hp1 | a0002 | c0002 | t0010 | g0224 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02965 | hp1 | a0001 | c0001 | t0033 | g0111 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0072 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03130 | hp1 | a0001 | c0001 | t0030 | g0154 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03130 | hp2 | a0003 | c0006 | t0043 | g0194 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03139 | hp2 | a0001 | c0001 | t0016 | g0018 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03195 | hp1 | a0001 | c0001 | t0011 | g0066 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0019 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0179 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03453 | hp2 | a0001 | c0001 | t0040 | g0064 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03486 | hp1 | a0001 | c0005 | t0001 | g0141 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | ESN | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03540 | hp2 | a0001 | c0004 | t0003 | g0039 | AFR | GWD | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0037 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03654 | hp2 | a0001 | c0001 | t0032 | g0182 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03669 | hp2 | a0001 | c0001 | t0031 | g0192 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03688 | hp2 | a0001 | c0001 | t0006 | g0071 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0156 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03831 | hp1 | a0001 | c0001 | t0007 | g0050 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03834 | hp2 | a0001 | c0001 | t0007 | g0012 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0178 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18522 | hp2 | a0001 | c0004 | t0003 | g0039 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18747 | hp1 | a0001 | c0001 | t0034 | g0087 | EAS | CHB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0059 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18906 | hp2 | a0002 | c0002 | t0010 | g0226 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18941 | hp1 | a0001 | c0001 | t0007 | g0127 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18956 | hp1 | a0005 | c0008 | t0001 | g0221 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18961 | hp2 | a0001 | c0001 | t0007 | g0150 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18962 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18986 | hp2 | a0001 | c0001 | t0026 | g0204 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18987 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18987 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18995 | hp2 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18997 | hp1 | a0001 | c0001 | t0019 | g0176 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19005 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19009 | hp2 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19063 | hp2 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19077 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19080 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19081 | hp2 | a0001 | c0001 | t0024 | g0100 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19086 | hp2 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA19240 | hp2 | a0001 | c0001 | t0014 | g0042 | AFR | YRI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ASW | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | GIH | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA20905 | hp2 | a0001 | c0001 | t0035 | g0140 | SAS | GIH | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01123 | hp1 | a0001 | c0001 | t0007 | g0158 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG03471 | hp2 | a0002 | c0002 | t0010 | g0225 | AFR | MSL | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | USA | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0041 | g0223 | REF | REF | GRSF1_chr4_70810783_70844890 | GRSF1 | chr4 | 70810783 | 70844890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:70836188
|
T | A | 1 | a0003 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.484A>T | p.Thr162Ser | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/10 | 547/6610 | 484/1443 | 162/480 | chr4 | 70836188 | ||
chr4:70836307
|
T | C | 1 | a0004 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.365A>G | p.Lys122Arg | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/10 | 428/6610 | 365/1443 | 122/480 | chr4 | 70836307 | ||
chr4:70839521
|
G | A | 1 | a0005 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.307C>T | p.Pro103Ser | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/10 | 370/6610 | 307/1443 | 103/480 | chr4 | 70839521 | ||
chr4:70839545
|
A | G | 4 | a0001a0003a0004others(1): Show | 324 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(321): Show |
missense_variant | MODERATE | c.283T>C | p.Ser95Pro | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/10 | 346/6610 | 283/1443 | 95/480 | chr4 | 70839545 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:70825327
|
A | G | 1 | a0001c0003 | 2 | HG02630.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.1362T>C | p.Val454Val | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/10 | 1425/6610 | 1362/1443 | 454/480 | chr4 | 70825327 | ||
chr4:70826183
|
G | A | 1 | a0001c0004 | 2 | HG03540.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.1198C>T | p.Leu400Leu | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/10 | 1261/6610 | 1198/1443 | 400/480 | chr4 | 70826183 | ||
chr4:70827946
|
A | C | 1 | a0001c0005 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1041T>G | p.Ala347Ala | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/10 | 1104/6610 | 1041/1443 | 347/480 | chr4 | 70827946 | ||
chr4:70839537
|
G | A | 1 | a0001c0009 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.291C>T | p.Leu97Leu | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/10 | 354/6610 | 291/1443 | 97/480 | chr4 | 70839537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:70816075
|
G | C | 2 | a0001c0001t0009a0001c0001t0044 | 7 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4812C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 8244 | chr4 | 70816075 | |||||
chr4:70816346
|
CA | C | 27 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(24): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*4540delT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7972 | chr4 | 70816346 | |||||
chr4:70816366
|
G | A | 1 | a0001c0001t0031 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4521C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7953 | chr4 | 70816366 | |||||
chr4:70816367
|
A | G | 1 | a0001c0001t0030 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4520T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7952 | chr4 | 70816367 | |||||
chr4:70816437
|
A | G | 1 | a0001c0001t0029 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4450T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7882 | chr4 | 70816437 | |||||
chr4:70816675
|
G | A | 3 | a0001c0001t0009a0001c0001t0012a0001c0001t0044 | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4212C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7644 | chr4 | 70816675 | |||||
chr4:70816687
|
A | G | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(37): Show | 290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*4200T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7632 | chr4 | 70816687 | |||||
chr4:70816711
|
C | T | 3 | a0001c0001t0015a0001c0001t0038a0001c0001t0039 | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4176G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7608 | chr4 | 70816711 | |||||
chr4:70816735
|
A | G | 1 | a0001c0001t0012 | 3 | HG00323.hp1 HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4152T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7584 | chr4 | 70816735 | |||||
chr4:70816810
|
T | C | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(33): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*4077A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7509 | chr4 | 70816810 | |||||
chr4:70816852
|
G | A | 1 | a0001c0001t0005 | 12 | NA18963.hp1 NA18963.hp2 NA18969.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4035C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7467 | chr4 | 70816852 | |||||
chr4:70816941
|
T | C | 1 | a0001c0001t0012 | 3 | HG00323.hp1 HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3946A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7378 | chr4 | 70816941 | |||||
chr4:70817023
|
CCACT | C | 3 | a0001c0001t0015a0001c0001t0038a0001c0001t0039 | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3860_*3863delAGTG | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7292 | chr4 | 70817023 | |||||
chr4:70817081
|
A | T | 1 | a0001c0001t0028 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3806T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7238 | chr4 | 70817081 | |||||
chr4:70817101
|
T | C | 1 | a0001c0001t0011 | 3 | HG02622.hp2 HG03195.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3786A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7218 | chr4 | 70817101 | |||||
chr4:70817151
|
G | C | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 327 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*3736C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7168 | chr4 | 70817151 | |||||
chr4:70817167
|
G | C | 33 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(30): Show | 275 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*3720C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7152 | chr4 | 70817167 | |||||
chr4:70817214
|
TGC | T | 2 | a0001c0001t0015a0001c0001t0038 | 3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3671_*3672delGC | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7103 | chr4 | 70817214 | |||||
chr4:70817216
|
C | CT | 5 | a0001c0001t0006a0001c0001t0011a0001c0001t0016others(2): Show | 18 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3670dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7102 | chr4 | 70817216 | |||||
chr4:70817269
|
C | T | 2 | a0001c0001t0015a0001c0001t0038 | 3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3618G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7050 | chr4 | 70817269 | |||||
chr4:70817287
|
G | A | 1 | a0001c0001t0044 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3600C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 7032 | chr4 | 70817287 | |||||
chr4:70817471
|
T | G | 1 | a0001c0001t0032 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3416A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6848 | chr4 | 70817471 | |||||
chr4:70817522
|
A | G | 1 | a0001c0001t0027 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3365T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6797 | chr4 | 70817522 | |||||
chr4:70817615
|
T | C | 2 | a0001c0001t0013a0001c0001t0033 | 3 | HG02258.hp2 HG02630.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3272A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6704 | chr4 | 70817615 | |||||
chr4:70817888
|
G | A | 2 | a0001c0001t0015a0001c0001t0038 | 3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2999C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6431 | chr4 | 70817888 | |||||
chr4:70817912
|
G | A | 1 | a0001c0001t0039 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2975C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6407 | chr4 | 70817912 | |||||
chr4:70817966
|
T | C | 2 | a0001c0001t0017a0001c0001t0034 | 2 | HG01884.hp1 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2921A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6353 | chr4 | 70817966 | |||||
chr4:70818118
|
A | G | 4 | a0001c0001t0002a0001c0001t0014a0001c0001t0022others(1): Show | 47 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2769T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6201 | chr4 | 70818118 | |||||
chr4:70818142
|
G | A | 1 | a0001c0001t0014 | 2 | HG02886.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2745C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6177 | chr4 | 70818142 | |||||
chr4:70818152
|
C | T | 1 | a0001c0001t0025 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2735G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6167 | chr4 | 70818152 | |||||
chr4:70818163
|
C | T | 1 | a0001c0001t0018 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2724G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6156 | chr4 | 70818163 | |||||
chr4:70818273
|
T | G | 1 | a0001c0001t0019 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2614A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 6046 | chr4 | 70818273 | |||||
chr4:70818644
|
C | G | 1 | a0001c0001t0015 | 2 | HG01167.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2243G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5675 | chr4 | 70818644 | |||||
chr4:70818694
|
G | A | 4 | a0001c0001t0006a0001c0001t0011a0001c0001t0016others(1): Show | 17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2193C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5625 | chr4 | 70818694 | |||||
chr4:70818699
|
C | A | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(37): Show | 290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*2188G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5620 | chr4 | 70818699 | |||||
chr4:70818741
|
G | A | 48 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | 324 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*2146C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5578 | chr4 | 70818741 | |||||
chr4:70818885
|
G | A | 1 | a0001c0001t0009 | 6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2002C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5434 | chr4 | 70818885 | |||||
chr4:70818904
|
A | G | 1 | a0001c0001t0009 | 6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1983T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5415 | chr4 | 70818904 | |||||
chr4:70819095
|
G | T | 1 | a0001c0001t0023 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1792C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5224 | chr4 | 70819095 | |||||
chr4:70819255
|
C | G | 1 | a0001c0001t0022 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1632G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 5064 | chr4 | 70819255 | |||||
chr4:70819321
|
T | C | 1 | a0001c0001t0008 | 6 | HG00609.hp1 HG02027.hp1 HG02056.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1566A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4998 | chr4 | 70819321 | |||||
chr4:70819375
|
C | A | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(33): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1512G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4944 | chr4 | 70819375 | |||||
chr4:70819430
|
C | T | 1 | a0001c0001t0016 | 2 | HG02818.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1457G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4889 | chr4 | 70819430 | |||||
chr4:70819486
|
T | C | 1 | a0001c0001t0035 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1401A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4833 | chr4 | 70819486 | |||||
chr4:70819619
|
A | G | 1 | a0001c0001t0021 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1268T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4700 | chr4 | 70819619 | |||||
chr4:70819663
|
T | C | 1 | a0003c0006t0043 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1224A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4656 | chr4 | 70819663 | |||||
chr4:70819811
|
A | G | 1 | a0001c0001t0040 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1076T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4508 | chr4 | 70819811 | |||||
chr4:70819830
|
T | C | 1 | a0001c0001t0036 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1057A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4489 | chr4 | 70819830 | |||||
chr4:70819863
|
G | GA | 3 | a0001c0001t0009a0001c0001t0012a0001c0001t0044 | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1023dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4455 | chr4 | 70819863 | |||||
chr4:70819924
|
A | C | 1 | a0001c0001t0020 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4395 | chr4 | 70819924 | |||||
chr4:70819982
|
G | A | 2 | a0001c0001t0009a0001c0001t0044 | 7 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*905C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4337 | chr4 | 70819982 | |||||
chr4:70820108
|
T | C | 1 | a0001c0001t0037 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*779A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4211 | chr4 | 70820108 | |||||
chr4:70820129
|
A | T | 3 | a0001c0001t0007a0001c0001t0018a0001c0001t0019 | 12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*758T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4190 | chr4 | 70820129 | |||||
chr4:70820169
|
T | C | 3 | a0001c0001t0015a0001c0001t0038a0001c0001t0039 | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*718A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 4150 | chr4 | 70820169 | |||||
chr4:70820529
|
C | G | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(36): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*358G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 3790 | chr4 | 70820529 | |||||
chr4:70820733
|
T | C | 3 | a0001c0001t0009a0001c0001t0012a0001c0001t0044 | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*154A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 10/10 | 3586 | chr4 | 70820733 | |||||
chr4:70839850
|
C | G | 1 | a0001c0001t0017 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/10 | 23 | chr4 | 70839850 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:70820883
|
T | C | 1 | a0001c0001t0007g0158 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.*26-22A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70820883 | ||||||
chr4:70821109
|
T | C | 1 | a0001c0001t0007g0050 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*26-248A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821109 | ||||||
chr4:70821164
|
C | T | 10 | a0001c0001t0007g0012a0001c0001t0007g0050a0001c0001t0007g0127others(7): Show | 12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.*26-303G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821164 | ||||||
chr4:70821235
|
C | T | 3 | a0001c0001t0012g0054a0001c0001t0012g0055a0001c0001t0012g0056 | 3 | HG00323.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.*26-374G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821235 | ||||||
chr4:70821407
|
G | A | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075 | 3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.*26-546C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821407 | ||||||
chr4:70821426
|
A | AAAAT | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.*26-569_*26-566dup others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821426 | ||||||
chr4:70821463
|
G | A | 2 | a0001c0001t0003g0217a0001c0001t0003g0218 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.*26-602C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821463 | ||||||
chr4:70821478
|
C | T | 1 | a0001c0001t0009g0016 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.*26-617G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821478 | ||||||
chr4:70821553
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.*26-692G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821553 | ||||||
chr4:70821566
|
A | G | 4 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(1): Show | 6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.*26-705T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821566 | ||||||
chr4:70821598
|
TC | T | 4 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075others(1): Show | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.*26-738delG | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821598 | ||||||
chr4:70821601
|
G | A | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*26-740C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821601 | ||||||
chr4:70821607
|
C | CA | 16 | a0001c0001t0001g0052a0001c0001t0001g0086a0001c0001t0001g0088others(13): Show | 16 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.*26-747dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821607 | ||||||
chr4:70821673
|
C | CT | 5 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0006g0067others(2): Show | 6 | HG02615.hp2 HG03209.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.*26-813dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821673 | ||||||
chr4:70821673
|
CT | C | 11 | a0001c0001t0001g0101a0001c0001t0001g0106a0001c0001t0001g0144others(8): Show | 11 | HG01167.hp2 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.*26-813delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821673 | ||||||
chr4:70821673
|
CTT | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 279 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.*26-814_*26-813del others(2): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821673 | ||||||
chr4:70821831
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.*26-970T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821831 | ||||||
chr4:70821962
|
C | T | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*26-1101G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70821962 | ||||||
chr4:70822110
|
C | T | 1 | a0001c0001t0006g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*26-1249G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822110 | ||||||
chr4:70822149
|
G | A | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*26-1288C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822149 | ||||||
chr4:70822149
|
G | C | 1 | a0001c0001t0012g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.*26-1288C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822149 | ||||||
chr4:70822312
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0028g0175 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.*26-1451C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822312 | ||||||
chr4:70822358
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.*26-1497C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822358 | ||||||
chr4:70822475
|
T | C | 1 | a0001c0001t0013g0105 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.*26-1614A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822475 | ||||||
chr4:70822482
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.*26-1621G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822482 | ||||||
chr4:70822542
|
C | T | 4 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075others(1): Show | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.*26-1681G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822542 | ||||||
chr4:70822583
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.*25+1703_*25+1710d others(10): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822583 | ||||||
chr4:70822593
|
AAAAAAAA others(6): Show |
A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 275 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.*25+1688_*25+1700d others(15): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822593 | ||||||
chr4:70822604
|
AAC | A | 22 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(19): Show | 30 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(27): Show |
intron_variant | MODIFIER | c.*25+1688_*25+1689d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822604 | ||||||
chr4:70822699
|
G | A | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075 | 3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.*25+1595C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822699 | ||||||
chr4:70822758
|
T | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0025others(26): Show | 43 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.*25+1536A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822758 | ||||||
chr4:70822767
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.*25+1527C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70822767 | ||||||
chr4:70823065
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.*25+1229G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823065 | ||||||
chr4:70823136
|
C | T | 3 | a0001c0001t0003g0045a0001c0001t0003g0216a0001c0001t0003g0219 | 4 | HG02717.hp1 NA19030.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.*25+1158G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823136 | ||||||
chr4:70823172
|
G | C | 13 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(10): Show | 17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.*25+1122C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823172 | ||||||
chr4:70823247
|
A | T | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075 | 3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.*25+1047T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823247 | ||||||
chr4:70823249
|
T | C | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*25+1045A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823249 | ||||||
chr4:70823264
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*25+1030C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823264 | ||||||
chr4:70823431
|
A | T | 2 | a0001c0001t0001g0097a0001c0001t0004g0092 | 2 | NA19004.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.*25+863T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823431 | ||||||
chr4:70823481
|
CT | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.*25+812delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823481 | ||||||
chr4:70823700
|
T | C | 10 | a0001c0001t0007g0012a0001c0001t0007g0050a0001c0001t0007g0127others(7): Show | 12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.*25+594A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823700 | ||||||
chr4:70823754
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0142 | 2 | NA18971.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.*25+540G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823754 | ||||||
chr4:70823809
|
G | A | 1 | a0001c0001t0001g0035 | 2 | NA18969.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.*25+485C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823809 | ||||||
chr4:70823812
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.*25+482C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823812 | ||||||
chr4:70823903
|
C | T | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.*25+391G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823903 | ||||||
chr4:70823968
|
A | C | 1 | a0001c0001t0038g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.*25+326T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823968 | ||||||
chr4:70823968
|
ATC | A | 2 | a0001c0001t0002g0211a0001c0001t0014g0042 | 3 | HG02809.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*25+324_*25+325del others(2): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823968 | ||||||
chr4:70823974
|
C | CT | 10 | a0001c0001t0006g0065a0001c0001t0009g0016a0001c0001t0009g0017others(7): Show | 12 | HG01517.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.*25+319dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823974 | ||||||
chr4:70823974
|
C | CTTT | 23 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0122others(20): Show | 28 | HG00673.hp2 HG01123.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.*25+319_*25+320ins others(3): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823974 | ||||||
chr4:70823974
|
C | CTTTT | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.*25+319_*25+320ins others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823974 | ||||||
chr4:70823974
|
C | CTTTTT | 27 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0091others(24): Show | 49 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.*25+319_*25+320ins others(5): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823974 | ||||||
chr4:70823976
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 319 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.*25+318G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70823976 | ||||||
chr4:70824002
|
G | A | 27 | a0001c0001t0001g0190a0001c0001t0002g0002a0001c0001t0002g0008others(24): Show | 49 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.*25+292C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824002 | ||||||
chr4:70824054
|
G | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.*25+240C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824054 | ||||||
chr4:70824066
|
G | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.*25+228C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824066 | ||||||
chr4:70824124
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*25+170A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824124 | ||||||
chr4:70824205
|
G | C | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*25+89C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824205 | ||||||
chr4:70824273
|
A | T | 1 | a0001c0001t0039g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.*25+21T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 9/9 | chr4 | 70824273 | ||||||
chr4:70824504
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.1394-136T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824504 | ||||||
chr4:70824539
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1394-171G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824539 | ||||||
chr4:70824647
|
G | C | 4 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075others(1): Show | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394-279C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824647 | ||||||
chr4:70824651
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 324 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.1394-283A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824651 | ||||||
chr4:70824675
|
C | T | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394-307G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824675 | ||||||
chr4:70824714
|
C | T | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394-346G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824714 | ||||||
chr4:70824729
|
G | A | 1 | a0001c0001t0036g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1394-361C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824729 | ||||||
chr4:70824762
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1394-394C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824762 | ||||||
chr4:70824859
|
T | G | 11 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(8): Show | 15 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1393+437A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824859 | ||||||
chr4:70824945
|
T | C | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1393+351A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824945 | ||||||
chr4:70824965
|
G | A | 13 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(10): Show | 17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1393+331C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824965 | ||||||
chr4:70824984
|
C | T | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075 | 3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1393+312G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824984 | ||||||
chr4:70824991
|
A | G | 1 | a0001c0001t0002g0200 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1393+305T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70824991 | ||||||
chr4:70825025
|
A | G | 1 | a0001c0001t0038g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1393+271T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70825025 | ||||||
chr4:70825111
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1393+185T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70825111 | ||||||
chr4:70825143
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1393+153A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70825143 | ||||||
chr4:70825197
|
T | C | 24 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(21): Show | 32 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.1393+99A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 8/9 | chr4 | 70825197 | ||||||
chr4:70825438
|
GACAA | G | 4 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075others(1): Show | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1258-11_1258-8delT others(3): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825438 | ||||||
chr4:70825565
|
G | T | 13 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(10): Show | 17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1258-134C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825565 | ||||||
chr4:70825566
|
C | T | 13 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(10): Show | 17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1258-135G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825566 | ||||||
chr4:70825822
|
C | G | 4 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(1): Show | 6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1257+302G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825822 | ||||||
chr4:70825823
|
T | G | 1 | a0001c0001t0005g0124 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1257+301A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825823 | ||||||
chr4:70825918
|
C | T | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1257+206G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825918 | ||||||
chr4:70825931
|
C | CA | 24 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(21): Show | 32 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257+192dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70825931 | ||||||
chr4:70826026
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1257+98G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70826026 | ||||||
chr4:70826068
|
C | A | 2 | a0001c0001t0001g0190a0001c0001t0028g0175 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1257+56G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70826068 | ||||||
chr4:70826113
|
C | T | 1 | a0001c0001t0040g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1257+11G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 7/9 | chr4 | 70826113 | ||||||
chr4:70826258
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0062a0001c0001t0001g0088others(6): Show | 12 | HG00639.hp2 HG01106.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1136-13T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826258 | ||||||
chr4:70826278
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0189 | 2 | HG02622.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1136-33T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826278 | ||||||
chr4:70826287
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1136-42A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826287 | ||||||
chr4:70826346
|
T | C | 1 | a0001c0001t0030g0154 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1136-101A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826346 | ||||||
chr4:70826457
|
G | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.1136-212C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826457 | ||||||
chr4:70826457
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1136-212C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826457 | ||||||
chr4:70826496
|
G | GA | 4 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075others(1): Show | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-252dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826496 | ||||||
chr4:70826521
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0029others(7): Show | 15 | HG01934.hp2 HG01978.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.1136-276A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826521 | ||||||
chr4:70826528
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 324 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.1136-283A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826528 | ||||||
chr4:70826536
|
G | GA | 14 | a0001c0001t0003g0045a0001c0001t0003g0061a0001c0001t0003g0216others(11): Show | 17 | HG00673.hp2 HG01123.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136-292dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826536 | ||||||
chr4:70826566
|
G | A | 5 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(2): Show | 7 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1136-321C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826566 | ||||||
chr4:70826592
|
C | A | 1 | a0001c0001t0009g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1136-347G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826592 | ||||||
chr4:70826672
|
T | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0142 | 2 | NA18971.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1136-427A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826672 | ||||||
chr4:70826753
|
T | A | 2 | a0001c0001t0004g0179a0001c0001t0031g0192 | 2 | HG03239.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1136-508A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826753 | ||||||
chr4:70826787
|
G | A | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1136-542C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70826787 | ||||||
chr4:70827181
|
G | A | 10 | a0001c0001t0007g0012a0001c0001t0007g0050a0001c0001t0007g0127others(7): Show | 12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.1135+671C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827181 | ||||||
chr4:70827196
|
G | T | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1135+656C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827196 | ||||||
chr4:70827203
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1135+649C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827203 | ||||||
chr4:70827220
|
G | A | 1 | a0001c0001t0038g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1135+632C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827220 | ||||||
chr4:70827235
|
C | G | 1 | a0001c0001t0005g0124 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1135+617G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827235 | ||||||
chr4:70827250
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1135+602A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827250 | ||||||
chr4:70827287
|
C | CA | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.1135+564dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827287 | ||||||
chr4:70827287
|
C | CAA | 8 | a0001c0001t0001g0062a0001c0001t0001g0109a0001c0001t0001g0112others(5): Show | 8 | HG00609.hp1 HG01952.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1135+563_1135+564d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827287 | ||||||
chr4:70827505
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0027others(6): Show | 13 | HG00609.hp2 HG01255.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1135+347G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827505 | ||||||
chr4:70827598
|
C | G | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1135+254G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827598 | ||||||
chr4:70827607
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1135+245T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827607 | ||||||
chr4:70827636
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1135+216G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827636 | ||||||
chr4:70827643
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0161 | 2 | HG01106.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1135+209G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827643 | ||||||
chr4:70827697
|
T | A | 3 | a0001c0001t0012g0054a0001c0001t0012g0055a0001c0001t0012g0056 | 3 | HG00323.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1135+155A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 6/9 | chr4 | 70827697 | ||||||
chr4:70828082
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0028g0175 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.951-46A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828082 | ||||||
chr4:70828542
|
G | GGACT | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.951-510_951-507dup others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828542 | ||||||
chr4:70828736
|
A | AT | 94 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 138 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.951-701dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828736 | ||||||
chr4:70828736
|
A | ATT | 5 | a0001c0001t0001g0021a0001c0001t0001g0088a0001c0001t0001g0121others(2): Show | 6 | HG01123.hp2 HG01978.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.951-702_951-701dup others(2): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828736 | ||||||
chr4:70828736
|
AT | A | 8 | a0001c0001t0001g0190a0001c0001t0003g0043a0001c0001t0003g0044others(5): Show | 10 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.951-701delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828736 | ||||||
chr4:70828746
|
T | G | 2 | a0001c0001t0001g0190a0001c0001t0028g0175 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.951-710A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828746 | ||||||
chr4:70828749
|
T | G | 2 | a0001c0001t0001g0190a0001c0001t0028g0175 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.951-713A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828749 | ||||||
chr4:70828763
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 275 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.951-727C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828763 | ||||||
chr4:70828803
|
T | C | 1 | a0001c0001t0004g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.951-767A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828803 | ||||||
chr4:70828874
|
A | G | 2 | a0001c0001t0011g0019a0001c0001t0011g0066 | 3 | HG02622.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.951-838T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828874 | ||||||
chr4:70828883
|
G | A | 2 | a0001c0001t0015g0073a0001c0001t0015g0074 | 2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.951-847C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828883 | ||||||
chr4:70828887
|
G | A | 4 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075others(1): Show | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.951-851C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828887 | ||||||
chr4:70828987
|
C | T | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075 | 3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.951-951G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70828987 | ||||||
chr4:70829014
|
T | C | 1 | a0001c0001t0001g0023 | 2 | HG02132.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.951-978A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829014 | ||||||
chr4:70829053
|
T | C | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.951-1017A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829053 | ||||||
chr4:70829131
|
T | C | 1 | a0001c0001t0032g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.951-1095A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829131 | ||||||
chr4:70829184
|
C | T | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.951-1148G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829184 | ||||||
chr4:70829350
|
GT | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.951-1315delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829350 | ||||||
chr4:70829360
|
T | C | 1 | a0001c0001t0034g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.951-1324A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829360 | ||||||
chr4:70829426
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.951-1390G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829426 | ||||||
chr4:70829442
|
G | A | 1 | a0001c0001t0039g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.951-1406C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829442 | ||||||
chr4:70829458
|
C | A | 2 | a0001c0001t0001g0190a0001c0001t0028g0175 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.951-1422G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829458 | ||||||
chr4:70829760
|
G | A | 4 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(1): Show | 6 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.951-1724C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829760 | ||||||
chr4:70829820
|
C | T | 1 | a0001c0001t0039g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.950+1719G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829820 | ||||||
chr4:70829824
|
G | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 207 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.950+1715C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829824 | ||||||
chr4:70829904
|
G | T | 1 | a0001c0001t0011g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.950+1635C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70829904 | ||||||
chr4:70830032
|
G | A | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.950+1507C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830032 | ||||||
chr4:70830056
|
C | T | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.950+1483G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830056 | ||||||
chr4:70830098
|
G | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.950+1441C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830098 | ||||||
chr4:70830157
|
G | A | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.950+1382C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830157 | ||||||
chr4:70830180
|
C | A | 1 | a0001c0001t0006g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.950+1359G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830180 | ||||||
chr4:70830181
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG02004.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.950+1358C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830181 | ||||||
chr4:70830199
|
G | A | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.950+1340C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830199 | ||||||
chr4:70830275
|
C | T | 4 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075others(1): Show | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+1264G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830275 | ||||||
chr4:70830350
|
C | T | 1 | a0001c0001t0001g0034 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.950+1189G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830350 | ||||||
chr4:70830358
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.950+1181A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830358 | ||||||
chr4:70830403
|
C | T | 1 | a0001c0001t0039g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.950+1136G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830403 | ||||||
chr4:70830404
|
C | A | 1 | a0001c0001t0039g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.950+1135G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830404 | ||||||
chr4:70830426
|
C | G | 9 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(6): Show | 11 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.950+1113G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830426 | ||||||
chr4:70830446
|
T | TA | 19 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0139others(16): Show | 24 | HG00673.hp2 HG01123.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.950+1092dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830446 | ||||||
chr4:70830459
|
A | C | 1 | a0001c0001t0039g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.950+1080T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830459 | ||||||
chr4:70830461
|
A | C | 9 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(6): Show | 11 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.950+1078T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830461 | ||||||
chr4:70830475
|
C | G | 11 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(8): Show | 15 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.950+1064G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830475 | ||||||
chr4:70830542
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.950+997C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830542 | ||||||
chr4:70830780
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 324 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.950+759T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830780 | ||||||
chr4:70830791
|
C | A | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.950+748G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830791 | ||||||
chr4:70830810
|
G | A | 28 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0025others(25): Show | 42 | HG00323.hp2 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.950+729C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830810 | ||||||
chr4:70830876
|
T | C | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.950+663A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830876 | ||||||
chr4:70830967
|
C | A | 1 | a0001c0001t0003g0218 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.950+572G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830967 | ||||||
chr4:70830999
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 275 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.950+540A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70830999 | ||||||
chr4:70831123
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.950+416G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831123 | ||||||
chr4:70831140
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.950+399T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831140 | ||||||
chr4:70831148
|
G | C | 2 | a0002c0002t0010g0224a0002c0002t0010g0225 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.950+391C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831148 | ||||||
chr4:70831212
|
G | A | 14 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(11): Show | 18 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.950+327C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831212 | ||||||
chr4:70831269
|
C | G | 1 | a0002c0002t0010g0224 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.950+270G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831269 | ||||||
chr4:70831301
|
G | C | 13 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(10): Show | 17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.950+238C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831301 | ||||||
chr4:70831355
|
C | CA | 5 | a0001c0001t0001g0114a0001c0001t0003g0045a0001c0001t0003g0061others(2): Show | 6 | HG00408.hp1 HG02717.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.950+183dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831355 | ||||||
chr4:70831432
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.950+107G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831432 | ||||||
chr4:70831476
|
G | T | 1 | a0001c0001t0042g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.950+63C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831476 | ||||||
chr4:70831479
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.950+60G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831479 | ||||||
chr4:70831519
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.950+20A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 5/9 | chr4 | 70831519 | ||||||
chr4:70831679
|
G | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0145a0005c0008t0001g0221 | 3 | NA18956.hp1 NA19057.hp2 NA19081.hp1 |
splice_region_variant&intron_variant | LOW | c.815-5C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831679 | ||||||
chr4:70831710
|
C | CT | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.815-37dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831710 | ||||||
chr4:70831793
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.815-119A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831793 | ||||||
chr4:70831832
|
G | T | 1 | a0001c0001t0001g0082 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.815-158C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831832 | ||||||
chr4:70831863
|
A | T | 1 | a0001c0001t0028g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.815-189T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831863 | ||||||
chr4:70831910
|
G | GT | 12 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(9): Show | 14 | HG00323.hp1 HG01167.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.815-237dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831910 | ||||||
chr4:70831910
|
GT | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.815-237delA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831910 | ||||||
chr4:70831975
|
C | T | 10 | a0001c0001t0007g0012a0001c0001t0007g0050a0001c0001t0007g0127others(7): Show | 12 | HG00673.hp2 HG01123.hp1 HG03710.hp1 others(9): Show |
intron_variant | MODIFIER | c.815-301G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70831975 | ||||||
chr4:70832112
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0028g0175 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.814+195G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832112 | ||||||
chr4:70832147
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.814+160A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832147 | ||||||
chr4:70832232
|
C | T | 3 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0004t0003g0039 | 4 | HG03209.hp2 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.814+75G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832232 | ||||||
chr4:70832233
|
T | A | 3 | a0001c0001t0003g0044a0001c0001t0003g0214a0001c0001t0003g0215 | 4 | HG02145.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.814+74A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832233 | ||||||
chr4:70832243
|
T | C | 1 | a0001c0009t0001g0222 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.814+64A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832243 | ||||||
chr4:70832282
|
C | T | 2 | a0002c0002t0010g0224a0002c0002t0010g0225 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.814+25G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 4/9 | chr4 | 70832282 | ||||||
chr4:70832466
|
C | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 324 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.671-16G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 3/9 | chr4 | 70832466 | ||||||
chr4:70832504
|
C | T | 1 | a0001c0001t0039g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.671-54G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 3/9 | chr4 | 70832504 | ||||||
chr4:70833079
|
T | C | 11 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(8): Show | 15 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+39A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 3/9 | chr4 | 70833079 | ||||||
chr4:70833281
|
T | C | 1 | a0001c0001t0039g0195 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.515-8A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833281 | ||||||
chr4:70833383
|
T | C | 4 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075others(1): Show | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.515-110A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833383 | ||||||
chr4:70833614
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.515-341A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833614 | ||||||
chr4:70833634
|
T | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(20): Show | 45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.515-361A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833634 | ||||||
chr4:70833688
|
C | T | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.515-415G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833688 | ||||||
chr4:70833756
|
TA | T | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.515-484delT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833756 | ||||||
chr4:70833794
|
C | T | 1 | a0001c0001t0021g0166 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.515-521G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833794 | ||||||
chr4:70833810
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.515-537G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70833810 | ||||||
chr4:70834138
|
T | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.515-865A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834138 | ||||||
chr4:70834174
|
C | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.515-901G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834174 | ||||||
chr4:70834219
|
A | T | 1 | a0001c0001t0037g0084 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.515-946T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834219 | ||||||
chr4:70834258
|
CA | C | 23 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(20): Show | 45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.515-986delT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834258 | ||||||
chr4:70834390
|
ATGTC | A | 4 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0214others(1): Show | 6 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.515-1121_515-1118d others(6): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834390 | ||||||
chr4:70834530
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(163): Show | 245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.515-1257A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834530 | ||||||
chr4:70834611
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.515-1338T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834611 | ||||||
chr4:70834637
|
T | C | 2 | a0001c0001t0001g0144a0001c0005t0001g0141 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.515-1364A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834637 | ||||||
chr4:70834778
|
C | T | 13 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(10): Show | 17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.514+1380G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834778 | ||||||
chr4:70834912
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.514+1246G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834912 | ||||||
chr4:70834924
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.514+1234G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70834924 | ||||||
chr4:70835009
|
T | C | 9 | a0001c0001t0001g0142a0001c0001t0009g0016a0001c0001t0009g0017others(6): Show | 11 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.514+1149A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835009 | ||||||
chr4:70835136
|
A | G | 2 | a0001c0001t0006g0067a0001c0001t0006g0068 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.514+1022T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835136 | ||||||
chr4:70835147
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.514+1011C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835147 | ||||||
chr4:70835218
|
C | G | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+940G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835218 | ||||||
chr4:70835391
|
C | T | 1 | a0001c0001t0004g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.514+767G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835391 | ||||||
chr4:70835424
|
G | A | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.514+734C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835424 | ||||||
chr4:70835428
|
C | CA | 14 | a0001c0001t0001g0049a0001c0001t0001g0147a0001c0001t0002g0008others(11): Show | 19 | HG00408.hp2 HG00438.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.514+729dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835428 | ||||||
chr4:70835442
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+716G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835442 | ||||||
chr4:70835443
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+715G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835443 | ||||||
chr4:70835444
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+714A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835444 | ||||||
chr4:70835446
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+712G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835446 | ||||||
chr4:70835448
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+710A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835448 | ||||||
chr4:70835449
|
AGTATGAT others(306): Show |
A | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514+396_514+708del | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835449 | ||||||
chr4:70835460
|
T | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 320 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.514+698A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835460 | ||||||
chr4:70835461
|
T | A | 4 | a0001c0001t0001g0143a0001c0001t0015g0073a0001c0001t0015g0074others(1): Show | 4 | HG01167.hp2 HG01515.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+697A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835461 | ||||||
chr4:70835488
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 278 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.514+670T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835488 | ||||||
chr4:70835585
|
T | C | 13 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(10): Show | 17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.514+573A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835585 | ||||||
chr4:70835595
|
T | C | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+563A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835595 | ||||||
chr4:70835631
|
C | T | 13 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(10): Show | 17 | HG01884.hp2 HG02145.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.514+527G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835631 | ||||||
chr4:70835663
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 215 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.514+495C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835663 | ||||||
chr4:70835677
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.514+481C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835677 | ||||||
chr4:70835682
|
C | A | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+476G>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835682 | ||||||
chr4:70835693
|
G | A | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.514+465C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835693 | ||||||
chr4:70835731
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.514+427C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835731 | ||||||
chr4:70835795
|
C | T | 4 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0214others(1): Show | 6 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.514+363G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835795 | ||||||
chr4:70835825
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.514+333A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835825 | ||||||
chr4:70835873
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 9 | HG02615.hp1 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.514+285C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70835873 | ||||||
chr4:70836016
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.514+142C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70836016 | ||||||
chr4:70836125
|
A | T | 1 | a0001c0001t0003g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.514+33T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 2/9 | chr4 | 70836125 | ||||||
chr4:70836406
|
A | T | 1 | a0001c0001t0009g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358-92T>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836406 | ||||||
chr4:70836541
|
GGTTT | G | 22 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(19): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.358-231_358-228del others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836541 | ||||||
chr4:70836584
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.358-270T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836584 | ||||||
chr4:70836586
|
T | A | 3 | a0001c0001t0003g0044a0001c0001t0003g0214a0001c0001t0003g0215 | 4 | HG02145.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-272A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836586 | ||||||
chr4:70836660
|
G | A | 3 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075 | 3 | HG01167.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.358-346C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836660 | ||||||
chr4:70836674
|
T | C | 1 | a0001c0001t0006g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.358-360A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836674 | ||||||
chr4:70836731
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0004g0077 | 2 | NA18999.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.358-417A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836731 | ||||||
chr4:70836839
|
G | A | 1 | a0001c0001t0039g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.358-525C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836839 | ||||||
chr4:70836876
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.358-562G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836876 | ||||||
chr4:70836896
|
T | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 324 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.358-582A>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836896 | ||||||
chr4:70836932
|
C | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.358-618G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836932 | ||||||
chr4:70836967
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 207 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.358-653A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70836967 | ||||||
chr4:70837030
|
T | G | 8 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(5): Show | 10 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.358-716A>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837030 | ||||||
chr4:70837147
|
G | A | 4 | a0001c0001t0015g0073a0001c0001t0015g0074a0001c0001t0038g0075others(1): Show | 4 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-833C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837147 | ||||||
chr4:70837194
|
A | C | 1 | a0001c0001t0004g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.358-880T>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837194 | ||||||
chr4:70837337
|
G | A | 1 | a0001c0001t0017g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.358-1023C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837337 | ||||||
chr4:70837368
|
G | T | 2 | a0001c0001t0002g0079a0001c0001t0002g0080 | 2 | NA18967.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.358-1054C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837368 | ||||||
chr4:70837393
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.358-1079A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837393 | ||||||
chr4:70837446
|
C | T | 1 | a0001c0001t0011g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.358-1132G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837446 | ||||||
chr4:70837483
|
G | C | 1 | a0001c0001t0004g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.358-1169C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837483 | ||||||
chr4:70837563
|
C | CA | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.358-1250dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837563 | ||||||
chr4:70837563
|
C | CAA | 27 | a0001c0001t0001g0038a0001c0001t0001g0119a0001c0001t0001g0120others(24): Show | 34 | HG00642.hp1 HG00673.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.358-1251_358-1250d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837563 | ||||||
chr4:70837664
|
G | T | 6 | a0001c0001t0005g0024a0001c0001t0005g0123a0001c0001t0005g0124others(3): Show | 7 | NA18969.hp1 NA18987.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.358-1350C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837664 | ||||||
chr4:70837695
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.358-1381A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837695 | ||||||
chr4:70837792
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.358-1478G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837792 | ||||||
chr4:70837812
|
A | AT | 5 | a0001c0001t0001g0122a0001c0001t0003g0043a0001c0001t0003g0044others(2): Show | 7 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.358-1499dupA | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837812 | ||||||
chr4:70837841
|
T | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.358-1527A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837841 | ||||||
chr4:70837887
|
G | A | 9 | a0001c0001t0001g0057a0001c0001t0009g0016a0001c0001t0009g0017others(6): Show | 11 | HG00323.hp1 HG00735.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.358-1573C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70837887 | ||||||
chr4:70838038
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.357+1433A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838038 | ||||||
chr4:70838219
|
C | CA | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 96 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.357+1251dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | ||||||
chr4:70838219
|
C | CAA | 38 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0027others(35): Show | 48 | HG00140.hp1 HG00140.hp2 HG01258.hp2 others(45): Show |
intron_variant | MODIFIER | c.357+1250_357+1251d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | ||||||
chr4:70838219
|
C | CAAA | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(66): Show | 113 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.357+1249_357+1251d others(5): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | ||||||
chr4:70838219
|
C | CAAAA | 12 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(9): Show | 14 | HG00642.hp2 HG01361.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.357+1248_357+1251d others(6): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | ||||||
chr4:70838219
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0009g0016a0001c0001t0009g0017a0001c0001t0009g0059others(1): Show | 6 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.357+1242_357+1251d others(12): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | ||||||
chr4:70838219
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0009g0060a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 4 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+1241_357+1251d others(13): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | ||||||
chr4:70838219
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0057 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.357+1238_357+1251d others(16): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | ||||||
chr4:70838219
|
CAA | C | 11 | a0001c0001t0006g0067a0001c0001t0006g0068a0001c0001t0006g0069others(8): Show | 12 | HG01167.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.357+1250_357+1251d others(4): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | ||||||
chr4:70838219
|
CAAA | C | 5 | a0001c0001t0006g0009a0001c0001t0006g0063a0001c0001t0006g0065others(2): Show | 8 | HG02818.hp1 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+1249_357+1251d others(5): Show |
GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838219 | ||||||
chr4:70838289
|
G | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(20): Show | 45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.357+1182C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838289 | ||||||
chr4:70838289
|
G | C | 1 | a0001c0001t0009g0060 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.357+1182C>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838289 | ||||||
chr4:70838311
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.357+1160G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838311 | ||||||
chr4:70838316
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0191 | 4 | HG01081.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+1155A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838316 | ||||||
chr4:70838327
|
G | GA | 23 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(20): Show | 45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.357+1143dupT | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838327 | ||||||
chr4:70838341
|
G | A | 11 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0045others(8): Show | 15 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.357+1130C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838341 | ||||||
chr4:70838463
|
T | C | 1 | a0005c0008t0001g0221 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.357+1008A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838463 | ||||||
chr4:70838558
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.357+913T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838558 | ||||||
chr4:70838844
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.357+627C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838844 | ||||||
chr4:70838953
|
C | T | 10 | a0001c0001t0001g0057a0001c0001t0003g0061a0001c0001t0009g0016others(7): Show | 12 | HG00323.hp1 HG00735.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.357+518G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838953 | ||||||
chr4:70838988
|
A | G | 1 | a0001c0004t0003g0039 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.357+483T>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70838988 | ||||||
chr4:70839038
|
G | A | 1 | a0001c0001t0031g0192 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.357+433C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839038 | ||||||
chr4:70839051
|
G | T | 1 | a0003c0006t0043g0194 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.357+420C>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839051 | ||||||
chr4:70839174
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.357+297A>G | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839174 | ||||||
chr4:70839248
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.357+223G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839248 | ||||||
chr4:70839279
|
C | G | 4 | a0001c0001t0001g0057a0001c0001t0012g0054a0001c0001t0012g0055others(1): Show | 4 | HG00323.hp1 HG00735.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+192G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839279 | ||||||
chr4:70839337
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+134C>T | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839337 | ||||||
chr4:70839390
|
C | G | 1 | a0001c0001t0036g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.357+81G>C | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839390 | ||||||
chr4:70839408
|
C | CG | 6 | a0001c0001t0001g0015a0001c0001t0001g0048a0001c0001t0001g0049others(3): Show | 7 | HG00438.hp2 HG01433.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+62dupC | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839408 | ||||||
chr4:70839414
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.357+57G>A | GRSF1 | ENSG00000132463.15 | transcript | ENST00000254799.11 | protein_coding | 1/9 | chr4 | 70839414 |