geneid | 221393 |
---|---|
ensemblid | ENSG00000153294.12 |
hgncid | 19011 |
symbol | ADGRF4 |
name | adhesion G protein-coupled receptor F4 |
refseq_nuc | NM_153838.5 |
refseq_prot | NP_722580.3 |
ensembl_nuc | ENST00000283303.3 |
ensembl_prot | ENSP00000283303.2 |
mane_status | MANE Select |
chr | chr6 |
start | 47698580 |
end | 47722014 |
strand | + |
ver | v1.2 |
region | chr6:47698580-47722014 |
region5000 | chr6:47693580-47727014 |
regionname0 | ADGRF4_chr6_47698580_47722014 |
regionname5000 | ADGRF4_chr6_47693580_47727014 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 695 | 307 | 58 | 70 | 143 | 12 | 23 | 111 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0002 | 1/0 | 695 | 69 | 33 | 4 | 20 | 2 | 9 | 17 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0003 | 0/0 | 695 | 6 | 0 | 1 | 5 | 0 | 0 | 4 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0004 | 0/0 | 695 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0005 | 0/0 | 695 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0006 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0007 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0008 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0009 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0010 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0011 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0012 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0013 | 0/0 | 695 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2088 | 296 | 52 | 68 | 140 | 12 | 23 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0002 | 1/0 | 2088 | 69 | 33 | 4 | 20 | 2 | 9 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0003 | 0/0 | 2088 | 6 | 5 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0004 | 0/0 | 2088 | 6 | 0 | 1 | 5 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0005 | 0/0 | 2088 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0006 | 0/0 | 2088 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0007 | 0/0 | 2088 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0008 | 0/0 | 2088 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0009 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0010 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0011 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0012 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0013 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0014 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0015 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
c0016 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1041 | 358 | 82 | 63 | 169 | 10 | 32 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0002 | 0/0 | 1040 | 17 | 0 | 12 | 0 | 4 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0003 | 0/0 | 1041 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0004 | 0/0 | 1041 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0005 | 0/0 | 1041 | 2 | 1 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0006 | 0/0 | 1041 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0007 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0008 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0009 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0010 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0011 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0012 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0013 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
t0014 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 46 | 5 | 18 | 10 | 4 | 8 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0002 | 0/0 | 38 | 4 | 6 | 23 | 2 | 3 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0003 | 0/0 | 32 | 0 | 4 | 28 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0004 | 0/0 | 28 | 0 | 7 | 20 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0005 | 0/0 | 21 | 0 | 4 | 11 | 1 | 5 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0006 | 0/0 | 16 | 2 | 10 | 0 | 3 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0007 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0008 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0011 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0019 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2088 | 296 | 52 | 68 | 140 | 12 | 23 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0003 | 0/0 | 2088 | 6 | 5 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0005 | 0/0 | 2088 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0007 | 0/0 | 2088 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0002c0002 | 1/0 | 2088 | 69 | 33 | 4 | 20 | 2 | 9 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0003c0004 | 0/0 | 2088 | 6 | 0 | 1 | 5 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0004c0006 | 0/0 | 2088 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0005c0008 | 0/0 | 2088 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0006c0014 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0007c0010 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0008c0013 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0009c0011 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0010c0012 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0011c0015 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0012c0016 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0013c0009 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3128 | 264 | 43 | 56 | 137 | 8 | 19 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0002 | 0/0 | 3127 | 17 | 0 | 12 | 0 | 4 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0003 | 0/0 | 3128 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0004 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0005 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0007 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0008 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0009 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0010 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0011 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0012 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0013 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0001t0014 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0003t0001 | 0/0 | 3128 | 6 | 5 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0005t0001 | 0/0 | 3128 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0001c0007t0001 | 0/0 | 3128 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0002c0002t0001 | 1/0 | 3128 | 68 | 32 | 4 | 20 | 2 | 9 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0002c0002t0005 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0003c0004t0001 | 0/0 | 3128 | 6 | 0 | 1 | 5 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0004c0006t0001 | 0/0 | 3128 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0005c0008t0006 | 0/0 | 3128 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0006c0014t0001 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0007c0010t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0008c0013t0001 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0009c0011t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0010c0012t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0011c0015t0004 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0012c0016t0001 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
a0013c0009t0001 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | copy fasta | chr6 | 47693580 | 47727014 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 43 | 4 | 18 | 9 | 4 | 7 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0002 | 0/0 | 38 | 4 | 6 | 23 | 2 | 3 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0003 | 0/0 | 30 | 0 | 4 | 26 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0004 | 0/0 | 25 | 0 | 7 | 17 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0008 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0011 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0002g0006 | 0/0 | 14 | 0 | 10 | 0 | 3 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0007g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0010g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0013g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0003t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0005t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0007t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0001c0007t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0005 | 0/0 | 16 | 0 | 3 | 8 | 1 | 4 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0007 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0019 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0002c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0003c0004t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0003c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0003c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0004c0006t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0005c0008t0006g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0006c0014t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0007c0010t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0008c0013t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0009c0011t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0010c0012t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0011c0015t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0012c0016t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
a0013c0009t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | GBR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0054 | EUR | FIN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | FIN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00642 | hp2 | a0001 | c0007 | t0001 | g0067 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01255 | hp2 | a0005 | c0008 | t0006 | g0026 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01358 | hp2 | a0003 | c0004 | t0001 | g0005 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02056 | hp2 | a0003 | c0004 | t0001 | g0061 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02129 | hp1 | a0001 | c0001 | t0013 | g0015 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02257 | hp2 | a0001 | c0007 | t0001 | g0056 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02572 | hp2 | a0011 | c0015 | t0004 | g0006 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02735 | hp1 | a0001 | c0001 | t0014 | g0001 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02970 | hp1 | a0002 | c0002 | t0005 | g0027 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02976 | hp2 | a0001 | c0001 | t0012 | g0012 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03017 | hp1 | a0013 | c0009 | t0001 | g0093 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03098 | hp2 | a0005 | c0008 | t0006 | g0026 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0130 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03688 | hp2 | a0001 | c0001 | t0007 | g0092 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03710 | hp2 | a0006 | c0014 | t0001 | g0005 | SAS | PJL | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03831 | hp1 | a0012 | c0016 | t0001 | g0099 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0036 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0063 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04115 | hp2 | a0008 | c0013 | t0001 | g0104 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0058 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18943 | hp2 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18954 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18954 | hp2 | a0009 | c0011 | t0001 | g0079 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18959 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18962 | hp2 | a0001 | c0005 | t0001 | g0127 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18968 | hp2 | a0004 | c0006 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18969 | hp1 | a0010 | c0012 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18972 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18994 | hp2 | a0004 | c0006 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19003 | hp2 | a0003 | c0004 | t0001 | g0113 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19043 | hp2 | a0007 | c0010 | t0001 | g0089 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19084 | hp1 | a0001 | c0001 | t0010 | g0076 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19086 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | YRI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | TSI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | USA | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | USA | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | USA | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | LWK | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0019 | REF | REF | ADGRF4_chr6_47693580_47727014 | ADGRF4 | chr6 | 47693580 | 47727014 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47707278
|
C | G | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.33C>G | p.Cys11Trp | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/10 | 264/3128 | 33/2088 | 11/695 | chr6 | 47707278 | ||
chr6:47712520
|
C | T | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.464C>T | p.Thr155Ile | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/10 | 695/3128 | 464/2088 | 155/695 | chr6 | 47712520 | ||
chr6:47713828
|
G | A | 1 | a0013 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.583G>A | p.Asp195Asn | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 814/3128 | 583/2088 | 195/695 | chr6 | 47713828 | ||
chr6:47713929
|
C | G | 1 | a0012 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.684C>G | p.His228Gln | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 915/3128 | 684/2088 | 228/695 | chr6 | 47713929 | ||
chr6:47713975
|
G | T | 1 | a0003 | 6 | HG01358.hp2 HG02056.hp2 NA18943.hp2 others(3): Show |
missense_variant | MODERATE | c.730G>T | p.Gly244Trp | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 961/3128 | 730/2088 | 244/695 | chr6 | 47713975 | ||
chr6:47713982
|
A | G | 1 | a0011 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.737A>G | p.His246Arg | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 968/3128 | 737/2088 | 246/695 | chr6 | 47713982 | ||
chr6:47714189
|
A | G | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.944A>G | p.Gln315Arg | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1175/3128 | 944/2088 | 315/695 | chr6 | 47714189 | ||
chr6:47714399
|
T | C | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1154T>C | p.Met385Thr | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1385/3128 | 1154/2088 | 385/695 | chr6 | 47714399 | ||
chr6:47714422
|
T | C | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1177T>C | p.Ser393Pro | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1408/3128 | 1177/2088 | 393/695 | chr6 | 47714422 | ||
chr6:47714531
|
G | A | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1286G>A | p.Arg429Gln | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1517/3128 | 1286/2088 | 429/695 | chr6 | 47714531 | ||
chr6:47714533
|
G | A | 1 | a0004 | 2 | NA18968.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.1288G>A | p.Val430Met | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1519/3128 | 1288/2088 | 430/695 | chr6 | 47714533 | ||
chr6:47714560
|
C | T | 1 | a0006 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1315C>T | p.Arg439Cys | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1546/3128 | 1315/2088 | 439/695 | chr6 | 47714560 | ||
chr6:47714783
|
G | A | 1 | a0007 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1538G>A | p.Arg513Gln | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1769/3128 | 1538/2088 | 513/695 | chr6 | 47714783 | ||
chr6:47714868
|
A | C | 9 | a0001a0004a0005others(6): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
missense_variant | MODERATE | c.1623A>C | p.Lys541Asn | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1854/3128 | 1623/2088 | 541/695 | chr6 | 47714868 | ||
chr6:47714935
|
A | G | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1690A>G | p.Ile564Val | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1921/3128 | 1690/2088 | 564/695 | chr6 | 47714935 | ||
chr6:47714946
|
C | G | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1701C>G | p.Phe567Leu | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1932/3128 | 1701/2088 | 567/695 | chr6 | 47714946 | ||
chr6:47714968
|
A | T | 1 | a0008 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1723A>T | p.Ile575Phe | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1954/3128 | 1723/2088 | 575/695 | chr6 | 47714968 | ||
chr6:47715107
|
G | C | 1 | a0009 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.1862G>C | p.Gly621Ala | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 2093/3128 | 1862/2088 | 621/695 | chr6 | 47715107 | ||
chr6:47716837
|
T | C | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1964T>C | p.Met655Thr | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/10 | 2195/3128 | 1964/2088 | 655/695 | chr6 | 47716837 | ||
chr6:47718417
|
C | G | 1 | a0005 | 2 | HG01255.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.2063C>G | p.Ser688Cys | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/10 | 2294/3128 | 2063/2088 | 688/695 | chr6 | 47718417 | ||
chr6:47718431
|
C | T | 1 | a0010 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.2077C>T | p.Arg693Cys | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/10 | 2308/3128 | 2077/2088 | 693/695 | chr6 | 47718431 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47712410
|
T | C | 1 | a0005c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.354T>C | p.His118His | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/10 | 585/3128 | 354/2088 | 118/695 | chr6 | 47712410 | ||
chr6:47712521
|
A | G | 1 | a0005c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.465A>G | p.Thr155Thr | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/10 | 696/3128 | 465/2088 | 155/695 | chr6 | 47712521 | ||
chr6:47712572
|
A | T | 1 | a0001c0007 | 2 | HG00642.hp2 HG02257.hp2 |
synonymous_variant | LOW | c.516A>T | p.Thr172Thr | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/10 | 747/3128 | 516/2088 | 172/695 | chr6 | 47712572 | ||
chr6:47714319
|
A | G | 1 | a0001c0005 | 3 | NA18962.hp2 NA18972.hp2 NA19086.hp1 |
synonymous_variant | LOW | c.1074A>G | p.Arg358Arg | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1305/3128 | 1074/2088 | 358/695 | chr6 | 47714319 | ||
chr6:47714523
|
G | A | 1 | a0005c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1278G>A | p.Val426Val | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1509/3128 | 1278/2088 | 426/695 | chr6 | 47714523 | ||
chr6:47714574
|
C | T | 1 | a0001c0003 | 6 | HG01243.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
synonymous_variant | LOW | c.1329C>T | p.Ile443Ile | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1560/3128 | 1329/2088 | 443/695 | chr6 | 47714574 | ||
chr6:47714937
|
C | T | 1 | a0005c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1692C>T | p.Ile564Ile | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1923/3128 | 1692/2088 | 564/695 | chr6 | 47714937 | ||
chr6:47714943
|
G | A | 1 | a0005c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1698G>A | p.Ala566Ala | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/10 | 1929/3128 | 1698/2088 | 566/695 | chr6 | 47714943 | ||
chr6:47717339
|
G | C | 1 | a0005c0008 | 2 | HG01255.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.2022G>C | p.Ser674Ser | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/10 | 2253/3128 | 2022/2088 | 674/695 | chr6 | 47717339 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47698637
|
C | T | 1 | a0001c0001t0014 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-174C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/10 | 8609 | chr6 | 47698637 | |||||
chr6:47698661
|
C | T | 1 | a0005c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-150C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/10 | 8585 | chr6 | 47698661 | |||||
chr6:47698734
|
T | G | 1 | a0005c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-77T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/10 | 8512 | chr6 | 47698734 | |||||
chr6:47721265
|
G | T | 1 | a0001c0001t0013 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2823 | chr6 | 47721265 | |||||
chr6:47721328
|
T | C | 1 | a0005c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*123T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2886 | chr6 | 47721328 | |||||
chr6:47721345
|
C | T | 1 | a0001c0001t0012 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2903 | chr6 | 47721345 | |||||
chr6:47721349
|
C | T | 1 | a0005c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*144C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2907 | chr6 | 47721349 | |||||
chr6:47721358
|
G | A | 1 | a0001c0001t0007 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*153G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 2916 | chr6 | 47721358 | |||||
chr6:47721541
|
G | C | 1 | a0001c0001t0008 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3099 | chr6 | 47721541 | |||||
chr6:47721640
|
T | C | 1 | a0001c0001t0009 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3198 | chr6 | 47721640 | |||||
chr6:47721641
|
C | T | 1 | a0005c0008t0006 | 2 | HG01255.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*436C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3199 | chr6 | 47721641 | |||||
chr6:47721670
|
T | A | 1 | a0001c0001t0010 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3228 | chr6 | 47721670 | |||||
chr6:47721692
|
C | T | 2 | a0001c0001t0003a0001c0001t0012 | 6 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*487C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3250 | chr6 | 47721692 | |||||
chr6:47721757
|
C | T | 1 | a0001c0001t0011 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3315 | chr6 | 47721757 | |||||
chr6:47721867
|
GA | G | 1 | a0001c0001t0002 | 17 | HG00323.hp2 HG00733.hp1 HG00738.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*671delA | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3434 | INFO_REALIGN_3_PRIME | chr6 | 47721867 | ||||
chr6:47721996
|
C | T | 2 | a0001c0001t0005a0002c0002t0005 | 2 | HG02970.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*791C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3554 | chr6 | 47721996 | |||||
chr6:47721997
|
G | T | 2 | a0001c0001t0004a0011c0015t0004 | 2 | HG02572.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*792G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 10/10 | 3555 | chr6 | 47721997 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47698859
|
C | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-17+65C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47698859 | ||||||
chr6:47698930
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+136C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47698930 | ||||||
chr6:47699005
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+211T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699005 | ||||||
chr6:47699042
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17+248A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699042 | ||||||
chr6:47699124
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+330T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699124 | ||||||
chr6:47699126
|
G | T | 3 | a0001c0001t0001g0042a0001c0001t0003g0012a0001c0001t0012g0012 | 7 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17+332G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699126 | ||||||
chr6:47699166
|
G | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-17+372G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699166 | ||||||
chr6:47699185
|
T | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-17+391T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699185 | ||||||
chr6:47699342
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+548G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699342 | ||||||
chr6:47699342
|
G | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-17+548G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699342 | ||||||
chr6:47699368
|
T | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+574T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699368 | ||||||
chr6:47699427
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+633A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699427 | ||||||
chr6:47699428
|
C | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+634C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699428 | ||||||
chr6:47699433
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+639G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699433 | ||||||
chr6:47699447
|
G | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-17+653G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699447 | ||||||
chr6:47699450
|
T | C | 1 | a0002c0002t0001g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17+656T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699450 | ||||||
chr6:47699499
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+705A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699499 | ||||||
chr6:47699509
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+715T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699509 | ||||||
chr6:47699559
|
A | G | 1 | a0002c0002t0001g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-17+765A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699559 | ||||||
chr6:47699575
|
A | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0040others(8): Show | 45 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-17+781A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699575 | ||||||
chr6:47699590
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+796G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699590 | ||||||
chr6:47699640
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+846T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699640 | ||||||
chr6:47699715
|
T | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+921T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699715 | ||||||
chr6:47699768
|
C | A | 1 | a0001c0001t0004g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-17+974C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699768 | ||||||
chr6:47699774
|
A | T | 1 | a0002c0002t0001g0039 | 2 | NA18977.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-17+980A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699774 | ||||||
chr6:47699853
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0053 | 9 | NA18945.hp1 NA18955.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17+1059G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699853 | ||||||
chr6:47699903
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1109T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699903 | ||||||
chr6:47699903
|
T | TAC | 68 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(65): Show | 182 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-17+1129_-17+1130d others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699903 | |||||
chr6:47699903
|
T | TACAC | 5 | a0001c0007t0001g0056a0002c0002t0001g0027a0002c0002t0001g0054others(2): Show | 5 | HG00280.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17+1127_-17+1130d others(6): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699903 | |||||
chr6:47699903
|
TACAC | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0023others(26): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-17+1127_-17+1130d others(6): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699903 | |||||
chr6:47699903
|
TACACAC | T | 2 | a0001c0003t0001g0018a0001c0003t0001g0123 | 5 | HG01243.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17+1125_-17+1130d others(8): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699903 | |||||
chr6:47699921
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-17+1127C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699921 | ||||||
chr6:47699925
|
G | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1131G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699925 | ||||||
chr6:47699927
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-17+1133C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699927 | ||||||
chr6:47699927
|
C | T | 1 | a0002c0002t0001g0039 | 2 | NA18977.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-17+1133C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699927 | ||||||
chr6:47699928
|
G | A | 2 | a0002c0002t0001g0027a0002c0002t0005g0027 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-17+1134G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699928 | ||||||
chr6:47699933
|
A | AC | 10 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0100others(7): Show | 16 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17+1150dupC | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699933 | |||||
chr6:47699933
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17+1139A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699933 | ||||||
chr6:47699933
|
AC | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(42): Show | 139 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.-17+1150delC | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699933 | |||||
chr6:47699933
|
ACC | A | 30 | a0001c0001t0001g0042a0001c0001t0001g0088a0001c0001t0003g0012others(27): Show | 60 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.-17+1149_-17+1150d others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47699933 | |||||
chr6:47699936
|
C | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1142C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699936 | ||||||
chr6:47699939
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1145C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699939 | ||||||
chr6:47699986
|
T | G | 2 | a0002c0002t0001g0027a0002c0002t0005g0027 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-17+1192T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47699986 | ||||||
chr6:47700045
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1251G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700045 | ||||||
chr6:47700047
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1253A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700047 | ||||||
chr6:47700057
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1263T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700057 | ||||||
chr6:47700071
|
A | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1277A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700071 | ||||||
chr6:47700106
|
A | G | 2 | a0002c0002t0001g0027a0002c0002t0005g0027 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-17+1312A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700106 | ||||||
chr6:47700113
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1319C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700113 | ||||||
chr6:47700204
|
AG | A | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1411delG | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700204 | ||||||
chr6:47700206
|
A | T | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1412A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700206 | ||||||
chr6:47700207
|
T | G | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1413T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700207 | ||||||
chr6:47700210
|
C | T | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1416C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700210 | ||||||
chr6:47700211
|
A | T | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-17+1417A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700211 | ||||||
chr6:47700277
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1483T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700277 | ||||||
chr6:47700300
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+1506G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700300 | ||||||
chr6:47700357
|
A | G | 2 | a0001c0001t0002g0031a0001c0001t0002g0085 | 3 | HG01081.hp1 HG01934.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-17+1563A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700357 | ||||||
chr6:47700523
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1729T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700523 | ||||||
chr6:47700636
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1842C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700636 | ||||||
chr6:47700761
|
A | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+1967A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700761 | ||||||
chr6:47700935
|
T | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(69): Show | 186 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-17+2141T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700935 | ||||||
chr6:47700938
|
A | ATTCTGAC others(20): Show |
1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2146_-17+2147i others(29): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47700938 | |||||
chr6:47700944
|
T | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2150T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700944 | ||||||
chr6:47700968
|
T | A | 1 | a0001c0001t0001g0102 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-17+2174T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700968 | ||||||
chr6:47700987
|
G | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(54): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-17+2193G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700987 | ||||||
chr6:47700988
|
G | T | 1 | a0002c0002t0001g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17+2194G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700988 | ||||||
chr6:47700989
|
G | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2195G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47700989 | ||||||
chr6:47701021
|
C | T | 3 | a0001c0001t0001g0088a0002c0002t0001g0032a0007c0010t0001g0089 | 4 | HG03453.hp1 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+2227C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701021 | ||||||
chr6:47701044
|
A | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 77 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-17+2250A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701044 | ||||||
chr6:47701144
|
C | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2350C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701144 | ||||||
chr6:47701185
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0023others(29): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-17+2391G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701185 | ||||||
chr6:47701315
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2521T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701315 | ||||||
chr6:47701364
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-17+2570C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701364 | ||||||
chr6:47701372
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2578G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701372 | ||||||
chr6:47701400
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.-17+2606G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701400 | ||||||
chr6:47701401
|
T | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.-17+2607T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701401 | ||||||
chr6:47701466
|
A | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(55): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-17+2672A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701466 | ||||||
chr6:47701476
|
G | A | 1 | a0008c0013t0001g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-17+2682G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701476 | ||||||
chr6:47701494
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0105 | 3 | HG02896.hp2 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-17+2700G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701494 | ||||||
chr6:47701693
|
A | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+2899A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701693 | ||||||
chr6:47701708
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(55): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-17+2914G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701708 | ||||||
chr6:47701750
|
A | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(49): Show | 141 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.-17+2956A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701750 | ||||||
chr6:47701920
|
G | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0023others(29): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-17+3126G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701920 | ||||||
chr6:47701937
|
G | A | 2 | a0002c0002t0001g0028a0002c0002t0001g0057 | 3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-17+3143G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701937 | ||||||
chr6:47701956
|
C | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3162C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701956 | ||||||
chr6:47701957
|
G | A | 1 | a0002c0002t0001g0025 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-17+3163G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47701957 | ||||||
chr6:47702015
|
A | G | 1 | a0001c0007t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-17+3221A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702015 | ||||||
chr6:47702026
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3232A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702026 | ||||||
chr6:47702058
|
C | G | 1 | a0001c0001t0001g0017 | 4 | HG02451.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+3264C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702058 | ||||||
chr6:47702100
|
A | G | 1 | a0001c0001t0004g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-17+3306A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702100 | ||||||
chr6:47702201
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-17+3407A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702201 | ||||||
chr6:47702254
|
GTGTGT | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0100 | 7 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17+3463_-17+3467d others(7): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47702254 | |||||
chr6:47702261
|
G | A | 1 | a0013c0009t0001g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-17+3467G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702261 | ||||||
chr6:47702302
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3508T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702302 | ||||||
chr6:47702407
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3613G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702407 | ||||||
chr6:47702434
|
T | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3640T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702434 | ||||||
chr6:47702443
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(49): Show | 141 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.-17+3649C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702443 | ||||||
chr6:47702474
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(56): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-17+3680T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702474 | ||||||
chr6:47702533
|
G | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(41): Show | 129 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-17+3739G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702533 | ||||||
chr6:47702645
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-17+3851C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702645 | ||||||
chr6:47702662
|
T | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+3868T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702662 | ||||||
chr6:47702879
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+4085G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702879 | ||||||
chr6:47702887
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17+4093C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702887 | ||||||
chr6:47702900
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+4106A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702900 | ||||||
chr6:47702939
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-17+4145G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702939 | ||||||
chr6:47702954
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-17+4160G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702954 | ||||||
chr6:47702990
|
T | C | 2 | a0002c0002t0001g0054a0002c0002t0001g0058 | 2 | HG00280.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-17+4196T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47702990 | ||||||
chr6:47703069
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-16-4161C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703069 | ||||||
chr6:47703288
|
C | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(48): Show | 140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.-16-3942C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703288 | ||||||
chr6:47703329
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-16-3901T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703329 | ||||||
chr6:47703407
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-3823G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703407 | ||||||
chr6:47703695
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-16-3535C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703695 | ||||||
chr6:47703696
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-16-3534A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703696 | ||||||
chr6:47703787
|
A | G | 1 | a0002c0002t0001g0025 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-16-3443A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703787 | ||||||
chr6:47703974
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-3256C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47703974 | ||||||
chr6:47704012
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(55): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-16-3218A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704012 | ||||||
chr6:47704053
|
C | CT | 7 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0088others(4): Show | 14 | HG01255.hp2 HG03098.hp2 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16-3164dupT | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47704053 | |||||
chr6:47704089
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-16-3141A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704089 | ||||||
chr6:47704187
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-3043A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704187 | ||||||
chr6:47704246
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(48): Show | 140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.-16-2984G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704246 | ||||||
chr6:47704280
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2950G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704280 | ||||||
chr6:47704327
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2903G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704327 | ||||||
chr6:47704333
|
A | C | 1 | a0001c0001t0001g0129 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-16-2897A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704333 | ||||||
chr6:47704367
|
C | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(48): Show | 140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.-16-2863C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704367 | ||||||
chr6:47704453
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2777T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704453 | ||||||
chr6:47704505
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2725A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704505 | ||||||
chr6:47704519
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-16-2711A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704519 | ||||||
chr6:47704543
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-16-2687G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704543 | ||||||
chr6:47704595
|
T | TCAAAATG others(317): Show |
1 | a0001c0001t0004g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-16-2622_-16-2621i others(326): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 47704595 | |||||
chr6:47704638
|
G | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2592G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704638 | ||||||
chr6:47704742
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2488T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704742 | ||||||
chr6:47704778
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2452G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704778 | ||||||
chr6:47704797
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2433G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47704797 | ||||||
chr6:47705072
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-16-2158A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705072 | ||||||
chr6:47705079
|
C | T | 1 | a0001c0001t0001g0011 | 6 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-2151C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705079 | ||||||
chr6:47705126
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-2104C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705126 | ||||||
chr6:47705139
|
G | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | NA18985.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-16-2091G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705139 | ||||||
chr6:47705178
|
C | T | 2 | a0002c0002t0001g0032a0007c0010t0001g0089 | 3 | HG03486.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-16-2052C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705178 | ||||||
chr6:47705181
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-16-2049C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705181 | ||||||
chr6:47705223
|
G | A | 1 | a0001c0001t0004g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-16-2007G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705223 | ||||||
chr6:47705254
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-16-1976G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705254 | ||||||
chr6:47705308
|
A | C | 1 | a0002c0002t0001g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-16-1922A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705308 | ||||||
chr6:47705323
|
G | T | 6 | a0002c0002t0001g0043a0002c0002t0001g0046a0002c0002t0001g0047others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-1907G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705323 | ||||||
chr6:47705342
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1888T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705342 | ||||||
chr6:47705344
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1886G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705344 | ||||||
chr6:47705457
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1773T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705457 | ||||||
chr6:47705469
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1761T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705469 | ||||||
chr6:47705567
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-16-1663T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705567 | ||||||
chr6:47705578
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-16-1652G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705578 | ||||||
chr6:47705664
|
A | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-1566A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47705664 | ||||||
chr6:47706030
|
T | C | 1 | a0001c0001t0001g0042 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-16-1200T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706030 | ||||||
chr6:47706110
|
A | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.-16-1120A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706110 | ||||||
chr6:47706288
|
A | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0082 | 2 | NA18961.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-16-942A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706288 | ||||||
chr6:47706351
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-16-879C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706351 | ||||||
chr6:47706414
|
G | A | 1 | a0001c0001t0001g0042 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-16-816G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706414 | ||||||
chr6:47706517
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-713C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706517 | ||||||
chr6:47706585
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-16-645T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706585 | ||||||
chr6:47706623
|
A | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(50): Show | 142 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-16-607A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706623 | ||||||
chr6:47706686
|
A | T | 1 | a0001c0007t0001g0067 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16-544A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706686 | ||||||
chr6:47706741
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-489G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706741 | ||||||
chr6:47706811
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-16-419C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706811 | ||||||
chr6:47706854
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-16-376A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706854 | ||||||
chr6:47706863
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-16-367A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706863 | ||||||
chr6:47706871
|
G | A | 1 | a0002c0002t0001g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-16-359G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706871 | ||||||
chr6:47706947
|
A | G | 1 | a0007c0010t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-16-283A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706947 | ||||||
chr6:47706983
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(54): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-16-247G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47706983 | ||||||
chr6:47707161
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0131 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-16-69C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47707161 | ||||||
chr6:47707183
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-16-47G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 1/9 | chr6 | 47707183 | ||||||
chr6:47707356
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.93+18C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707356 | ||||||
chr6:47707366
|
C | T | 1 | a0001c0003t0001g0123 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93+28C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707366 | ||||||
chr6:47707375
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.93+37A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707375 | ||||||
chr6:47707377
|
C | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.93+39C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707377 | ||||||
chr6:47707553
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.93+215C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707553 | ||||||
chr6:47707561
|
G | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0023others(29): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.93+223G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707561 | ||||||
chr6:47707614
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.93+276C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707614 | ||||||
chr6:47707619
|
A | G | 1 | a0002c0002t0001g0020 | 3 | NA18962.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.93+281A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707619 | ||||||
chr6:47707738
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(21): Show | 88 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.93+400A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707738 | ||||||
chr6:47707770
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.93+432T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707770 | ||||||
chr6:47707814
|
T | A | 1 | a0007c0010t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.94-410T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707814 | ||||||
chr6:47707850
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.94-374G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47707850 | ||||||
chr6:47708034
|
G | A | 2 | a0002c0002t0001g0032a0002c0002t0001g0046 | 3 | HG03486.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.94-190G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708034 | ||||||
chr6:47708043
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.94-181C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708043 | ||||||
chr6:47708061
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.94-163A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708061 | ||||||
chr6:47708130
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94-94C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708130 | ||||||
chr6:47708150
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-74A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708150 | ||||||
chr6:47708152
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-72G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708152 | ||||||
chr6:47708153
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-71G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708153 | ||||||
chr6:47708155
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-69G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708155 | ||||||
chr6:47708156
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-68C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708156 | ||||||
chr6:47708157
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-67C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708157 | ||||||
chr6:47708158
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-66T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708158 | ||||||
chr6:47708159
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-65C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708159 | ||||||
chr6:47708161
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-63A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708161 | ||||||
chr6:47708163
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-61G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708163 | ||||||
chr6:47708164
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-60C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708164 | ||||||
chr6:47708166
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94-58G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708166 | ||||||
chr6:47708186
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(34): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.94-38C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 2/9 | chr6 | 47708186 | ||||||
chr6:47708298
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.148+20T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708298 | ||||||
chr6:47708375
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+97C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708375 | ||||||
chr6:47708402
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+124C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708402 | ||||||
chr6:47708414
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.148+136C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708414 | ||||||
chr6:47708448
|
T | C | 1 | a0001c0001t0001g0034 | 2 | HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.148+170T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708448 | ||||||
chr6:47708450
|
C | T | 1 | a0001c0001t0007g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.148+172C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708450 | ||||||
chr6:47708513
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+235A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708513 | ||||||
chr6:47708624
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+346G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708624 | ||||||
chr6:47708660
|
C | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+382C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708660 | ||||||
chr6:47708707
|
A | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(50): Show | 142 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.148+429A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708707 | ||||||
chr6:47708759
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+481G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708759 | ||||||
chr6:47708783
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+505T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708783 | ||||||
chr6:47708889
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+611T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708889 | ||||||
chr6:47708890
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+612T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708890 | ||||||
chr6:47708955
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.148+677T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47708955 | ||||||
chr6:47709006
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.148+728C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709006 | ||||||
chr6:47709077
|
C | CAAGGTTT others(93): Show |
1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+807_148+808ins others(100): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47709077 | |||||
chr6:47709096
|
G | A | 2 | a0001c0001t0002g0031a0001c0001t0002g0085 | 3 | HG01081.hp1 HG01934.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.148+818G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709096 | ||||||
chr6:47709104
|
T | G | 3 | a0001c0001t0004g0052a0001c0007t0001g0056a0001c0007t0001g0067 | 3 | HG00642.hp2 HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.148+826T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709104 | ||||||
chr6:47709223
|
T | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0088a0001c0001t0003g0012others(2): Show | 9 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.148+945T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709223 | ||||||
chr6:47709238
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.148+960A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709238 | ||||||
chr6:47709254
|
A | G | 1 | a0012c0016t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.148+976A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709254 | ||||||
chr6:47709291
|
C | T | 2 | a0001c0007t0001g0056a0001c0007t0001g0067 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.148+1013C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709291 | ||||||
chr6:47709362
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(21): Show | 88 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.148+1084T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709362 | ||||||
chr6:47709451
|
A | T | 1 | a0002c0002t0001g0025 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.148+1173A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709451 | ||||||
chr6:47709479
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.148+1201A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709479 | ||||||
chr6:47709502
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+1224A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709502 | ||||||
chr6:47709582
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-1153T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709582 | ||||||
chr6:47709639
|
T | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-1096T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709639 | ||||||
chr6:47709710
|
G | A | 2 | a0002c0002t0001g0028a0002c0002t0001g0057 | 3 | HG01891.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149-1025G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709710 | ||||||
chr6:47709849
|
G | GTTTT | 24 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(21): Show | 91 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.149-879_149-876dup others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47709849 | |||||
chr6:47709849
|
G | GTTTTT | 30 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0023others(27): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.149-880_149-876dup others(5): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47709849 | |||||
chr6:47709860
|
G | T | 4 | a0001c0001t0001g0042a0001c0001t0003g0012a0001c0001t0003g0066others(1): Show | 8 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-875G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709860 | ||||||
chr6:47709925
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-810C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709925 | ||||||
chr6:47709958
|
AATGTGTC others(2): Show |
A | 2 | a0002c0002t0001g0013a0002c0002t0001g0060 | 5 | NA18939.hp2 NA18940.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-773_149-765del others(9): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47709958 | |||||
chr6:47709969
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-766T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709969 | ||||||
chr6:47709980
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.149-755C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47709980 | ||||||
chr6:47710051
|
G | A | 2 | a0002c0002t0001g0027a0002c0002t0005g0027 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.149-684G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710051 | ||||||
chr6:47710095
|
C | A | 1 | a0003c0004t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.149-640C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710095 | ||||||
chr6:47710150
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(50): Show | 142 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.149-585G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710150 | ||||||
chr6:47710199
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(54): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.149-536A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710199 | ||||||
chr6:47710393
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-342C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710393 | ||||||
chr6:47710446
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(23): Show | 93 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.149-289C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710446 | ||||||
chr6:47710475
|
C | A | 1 | a0002c0002t0001g0062 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.149-260C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710475 | ||||||
chr6:47710543
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.149-192T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710543 | ||||||
chr6:47710551
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149-184G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710551 | ||||||
chr6:47710577
|
C | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-158C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710577 | ||||||
chr6:47710653
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.149-82G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710653 | ||||||
chr6:47710676
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.149-59A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710676 | ||||||
chr6:47710719
|
CT | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.149-9delT | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 47710719 | |||||
chr6:47710722
|
T | C | 1 | a0002c0002t0001g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.149-13T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 3/9 | chr6 | 47710722 | ||||||
chr6:47710922
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+36A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47710922 | ||||||
chr6:47710942
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.300+56C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47710942 | ||||||
chr6:47710982
|
C | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(49): Show | 141 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.300+96C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47710982 | ||||||
chr6:47710983
|
A | G | 1 | a0002c0002t0001g0065 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.300+97A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47710983 | ||||||
chr6:47711077
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+191T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711077 | ||||||
chr6:47711093
|
C | G | 1 | a0002c0002t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.300+207C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711093 | ||||||
chr6:47711112
|
CA | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(45): Show | 133 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.300+243delA | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 47711112 | |||||
chr6:47711112
|
CAA | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(56): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.300+242_300+243del others(2): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 47711112 | |||||
chr6:47711125
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(54): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.300+239A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711125 | ||||||
chr6:47711240
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+354A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711240 | ||||||
chr6:47711280
|
T | C | 1 | a0002c0002t0001g0007 | 11 | HG01069.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+394T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711280 | ||||||
chr6:47711366
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.300+480A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711366 | ||||||
chr6:47711477
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0029 | 6 | HG01175.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+591G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711477 | ||||||
chr6:47711540
|
C | T | 1 | a0001c0001t0001g0042 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.300+654C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711540 | ||||||
chr6:47711550
|
C | A | 1 | a0012c0016t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.300+664C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711550 | ||||||
chr6:47711550
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.300+664C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711550 | ||||||
chr6:47711555
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+669C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711555 | ||||||
chr6:47711621
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.300+735A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711621 | ||||||
chr6:47711796
|
G | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-561G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711796 | ||||||
chr6:47711850
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-507A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711850 | ||||||
chr6:47711889
|
G | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(33): Show | 103 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.301-468G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711889 | ||||||
chr6:47711900
|
AG | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.301-456delG | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47711900 | ||||||
chr6:47712053
|
G | A | 1 | a0001c0007t0001g0067 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.301-304G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712053 | ||||||
chr6:47712055
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-302T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712055 | ||||||
chr6:47712096
|
A | G | 1 | a0001c0001t0004g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.301-261A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712096 | ||||||
chr6:47712100
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0088a0001c0001t0003g0012others(2): Show | 9 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.301-257G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712100 | ||||||
chr6:47712180
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-177T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712180 | ||||||
chr6:47712184
|
C | A | 1 | a0001c0001t0001g0124 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.301-173C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 4/9 | chr6 | 47712184 | ||||||
chr6:47712625
|
A | G | 1 | a0002c0002t0001g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+17A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712625 | ||||||
chr6:47712714
|
A | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(48): Show | 140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.552+106A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712714 | ||||||
chr6:47712847
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+239G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712847 | ||||||
chr6:47712870
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.552+262G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712870 | ||||||
chr6:47712882
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0098 | 4 | HG01099.hp2 HG01123.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+274A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712882 | ||||||
chr6:47712936
|
G | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(48): Show | 140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.552+328G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712936 | ||||||
chr6:47712979
|
G | A | 1 | a0002c0002t0001g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.552+371G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47712979 | ||||||
chr6:47713025
|
G | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+417G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713025 | ||||||
chr6:47713260
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.553-538T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713260 | ||||||
chr6:47713275
|
A | AT | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.553-523_553-522ins others(1): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713275 | ||||||
chr6:47713297
|
A | T | 1 | a0001c0001t0004g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.553-501A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713297 | ||||||
chr6:47713451
|
T | G | 1 | a0002c0002t0001g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.553-347T>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713451 | ||||||
chr6:47713505
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.553-293A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713505 | ||||||
chr6:47713758
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.553-40T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 5/9 | chr6 | 47713758 | ||||||
chr6:47715213
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(34): Show | 105 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1932+36C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715213 | ||||||
chr6:47715255
|
A | C | 1 | a0001c0001t0001g0016 | 4 | HG00544.hp2 NA18942.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1932+78A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715255 | ||||||
chr6:47715321
|
A | G | 46 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(43): Show | 131 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1932+144A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715321 | ||||||
chr6:47715428
|
G | A | 2 | a0001c0007t0001g0056a0001c0007t0001g0067 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1932+251G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715428 | ||||||
chr6:47715615
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0095others(1): Show | 14 | HG00741.hp1 HG02451.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1932+438A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715615 | ||||||
chr6:47715682
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0088a0001c0001t0003g0012others(2): Show | 9 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1932+505C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715682 | ||||||
chr6:47715696
|
G | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+519G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715696 | ||||||
chr6:47715757
|
G | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+580G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715757 | ||||||
chr6:47715776
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+599A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715776 | ||||||
chr6:47715827
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+650T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715827 | ||||||
chr6:47715864
|
A | G | 1 | a0002c0002t0001g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1932+687A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715864 | ||||||
chr6:47715900
|
C | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1932+723C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715900 | ||||||
chr6:47715900
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 223 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1932+723C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715900 | ||||||
chr6:47715935
|
A | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1932+758A>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715935 | ||||||
chr6:47715983
|
A | ATT | 5 | a0002c0002t0001g0027a0002c0002t0001g0032a0002c0002t0001g0046others(2): Show | 6 | HG02451.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1933-808_1933-807d others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 47715983 | |||||
chr6:47715983
|
AT | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0023others(29): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1933-807delT | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 47715983 | |||||
chr6:47715983
|
ATT | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(22): Show | 90 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1933-808_1933-807d others(4): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 47715983 | |||||
chr6:47715998
|
T | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.1933-808T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715998 | ||||||
chr6:47715998
|
T | TA | 13 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0021others(10): Show | 34 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1933-808_1933-807i others(3): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715998 | ||||||
chr6:47715999
|
T | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.1933-807T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47715999 | ||||||
chr6:47716033
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1933-773C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716033 | ||||||
chr6:47716099
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-707T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716099 | ||||||
chr6:47716217
|
C | CCTGTGAC others(7): Show |
1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-587_1933-586i others(16): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 47716217 | |||||
chr6:47716417
|
C | T | 1 | a0002c0002t0001g0025 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1933-389C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716417 | ||||||
chr6:47716473
|
T | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-333T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716473 | ||||||
chr6:47716487
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-319C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716487 | ||||||
chr6:47716653
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-153C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716653 | ||||||
chr6:47716659
|
A | G | 1 | a0002c0002t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1933-147A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716659 | ||||||
chr6:47716670
|
A | G | 2 | a0002c0002t0001g0047a0002c0002t0001g0049 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1933-136A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716670 | ||||||
chr6:47716727
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-79T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716727 | ||||||
chr6:47716741
|
G | A | 1 | a0002c0002t0001g0032 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1933-65G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716741 | ||||||
chr6:47716748
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-58A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716748 | ||||||
chr6:47716755
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-51G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716755 | ||||||
chr6:47716771
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1933-35A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716771 | ||||||
chr6:47716775
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1933-31T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716775 | ||||||
chr6:47716799
|
G | T | 5 | a0002c0002t0001g0027a0002c0002t0001g0032a0002c0002t0001g0046others(2): Show | 6 | HG02451.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1933-7G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 6/9 | chr6 | 47716799 | ||||||
chr6:47716855
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
splice_region_variant&intron_variant | LOW | c.1974+8G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/9 | chr6 | 47716855 | ||||||
chr6:47716886
|
T | C | 5 | a0002c0002t0001g0027a0002c0002t0001g0032a0002c0002t0001g0046others(2): Show | 6 | HG02451.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1974+39T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/9 | chr6 | 47716886 | ||||||
chr6:47716969
|
G | T | 1 | a0001c0001t0001g0042 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1974+122G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/9 | chr6 | 47716969 | ||||||
chr6:47717191
|
T | C | 3 | a0001c0001t0003g0012a0001c0001t0003g0066a0001c0001t0012g0012 | 6 | HG02258.hp1 HG02717.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1975-101T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 7/9 | chr6 | 47717191 | ||||||
chr6:47717384
|
G | A | 1 | a0001c0001t0004g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2034+33G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717384 | ||||||
chr6:47717421
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2034+70C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717421 | ||||||
chr6:47717549
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2034+198G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717549 | ||||||
chr6:47717586
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2034+235T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717586 | ||||||
chr6:47717740
|
C | G | 1 | a0002c0002t0001g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2034+389C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717740 | ||||||
chr6:47717919
|
C | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0023others(22): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2035-470C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47717919 | ||||||
chr6:47718098
|
C | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0078others(1): Show | 6 | HG02015.hp1 HG02129.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2035-291C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718098 | ||||||
chr6:47718103
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2035-286T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718103 | ||||||
chr6:47718107
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0101 | 2 | NA18978.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2035-282C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718107 | ||||||
chr6:47718129
|
T | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2035-260T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718129 | ||||||
chr6:47718167
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2035-222G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718167 | ||||||
chr6:47718215
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2035-174C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718215 | ||||||
chr6:47718228
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2035-161A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718228 | ||||||
chr6:47718342
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2035-47T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718342 | ||||||
chr6:47718365
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2035-24T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 8/9 | chr6 | 47718365 | ||||||
chr6:47718498
|
C | G | 2 | a0001c0007t0001g0056a0001c0007t0001g0067 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.*3+53C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718498 | ||||||
chr6:47718499
|
C | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(48): Show | 140 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.*3+54C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718499 | ||||||
chr6:47718635
|
G | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+190G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718635 | ||||||
chr6:47718661
|
AT | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.*3+217delT | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718661 | ||||||
chr6:47718674
|
T | A | 1 | a0002c0002t0001g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.*3+229T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718674 | ||||||
chr6:47718729
|
A | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+284A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718729 | ||||||
chr6:47718856
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.*3+411C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718856 | ||||||
chr6:47718884
|
A | G | 1 | a0007c0010t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*3+439A>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47718884 | ||||||
chr6:47719051
|
G | A | 1 | a0001c0007t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*3+606G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719051 | ||||||
chr6:47719063
|
C | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.*3+618C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719063 | ||||||
chr6:47719163
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.*3+718T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719163 | ||||||
chr6:47719271
|
T | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(40): Show | 128 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.*3+826T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719271 | ||||||
chr6:47719424
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.*3+979G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719424 | ||||||
chr6:47719497
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.*3+1052G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719497 | ||||||
chr6:47719518
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+1073C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719518 | ||||||
chr6:47719648
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.*3+1203G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719648 | ||||||
chr6:47719657
|
C | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+1212C>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719657 | ||||||
chr6:47719666
|
G | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+1221G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719666 | ||||||
chr6:47719794
|
C | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*3+1349C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719794 | ||||||
chr6:47719881
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-1328T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719881 | ||||||
chr6:47719922
|
G | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0119 | 4 | HG00558.hp1 NA18945.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-1287G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719922 | ||||||
chr6:47719949
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.*4-1260G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719949 | ||||||
chr6:47719987
|
C | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-1222C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47719987 | ||||||
chr6:47720082
|
C | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0125 | 4 | NA18978.hp2 NA19011.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-1127C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720082 | ||||||
chr6:47720119
|
GATTACAG others(3): Show |
G | 1 | a0001c0005t0001g0127 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.*4-1088_*4-1079del others(10): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 47720119 | |||||
chr6:47720188
|
C | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-1021C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720188 | ||||||
chr6:47720205
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-1004G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720205 | ||||||
chr6:47720279
|
G | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-930G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720279 | ||||||
chr6:47720366
|
G | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(53): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.*4-843G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720366 | ||||||
chr6:47720380
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-829G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720380 | ||||||
chr6:47720392
|
G | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 85 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.*4-817G>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720392 | ||||||
chr6:47720456
|
A | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-753A>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720456 | ||||||
chr6:47720476
|
C | T | 21 | a0002c0002t0001g0005a0002c0002t0001g0013a0002c0002t0001g0020others(18): Show | 46 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.*4-733C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720476 | ||||||
chr6:47720598
|
T | C | 5 | a0002c0002t0001g0027a0002c0002t0001g0032a0002c0002t0001g0046others(2): Show | 6 | HG02451.hp2 HG02970.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-611T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720598 | ||||||
chr6:47720600
|
G | A | 1 | a0001c0007t0001g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*4-609G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720600 | ||||||
chr6:47720772
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*4-437G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720772 | ||||||
chr6:47720856
|
G | T | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-353G>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720856 | ||||||
chr6:47720870
|
C | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(40): Show | 128 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.*4-339C>T | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720870 | ||||||
chr6:47720880
|
T | C | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-329T>C | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720880 | ||||||
chr6:47720932
|
C | G | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-277C>G | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720932 | ||||||
chr6:47720933
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-276G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47720933 | ||||||
chr6:47721021
|
GCCTTTTT others(12): Show |
G | 1 | a0001c0001t0010g0076 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.*4-187_*4-169delCC others(17): Show |
ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47721021 | ||||||
chr6:47721117
|
G | A | 1 | a0005c0008t0006g0026 | 2 | HG01255.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*4-92G>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47721117 | ||||||
chr6:47721186
|
T | A | 1 | a0001c0001t0002g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.*4-23T>A | ADGRF4 | ENSG00000153294.12 | transcript | ENST00000283303.3 | protein_coding | 9/9 | chr6 | 47721186 |