geneid | 266977 |
---|---|
ensemblid | ENSG00000153292.16 |
hgncid | 18990 |
symbol | ADGRF1 |
name | adhesion G protein-coupled receptor F1 |
refseq_nuc | NM_153840.4 |
refseq_prot | NP_722582.2 |
ensembl_nuc | ENST00000371253.7 |
ensembl_prot | ENSP00000360299.2 |
mane_status | MANE Select |
chr | chr6 |
start | 46997708 |
end | 47042332 |
strand | - |
ver | v1.2 |
region | chr6:46997708-47042332 |
region5000 | chr6:46992708-47047332 |
regionname0 | ADGRF1_chr6_46997708_47042332 |
regionname5000 | ADGRF1_chr6_46992708_47047332 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 910 | 284 | 44 | 54 | 144 | 9 | 31 | 116 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002 | 0/0 | 910 | 84 | 38 | 12 | 33 | 0 | 1 | 25 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0003 | 0/0 | 910 | 9 | 2 | 5 | 0 | 1 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0004 | 0/0 | 910 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0005 | 0/0 | 910 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0006 | 0/0 | 910 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0007 | 0/0 | 910 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0008 | 0/0 | 910 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0009 | 0/0 | 910 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0010 | 0/0 | 523 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0011 | 0/0 | 910 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0012 | 0/0 | 910 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0013 | 0/0 | 910 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0014 | 0/0 | 910 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0015 | 0/0 | 910 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2733 | 256 | 29 | 44 | 142 | 9 | 31 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0002 | 0/0 | 2733 | 76 | 31 | 11 | 33 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0003 | 0/1 | 2733 | 13 | 9 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0004 | 0/0 | 2733 | 9 | 2 | 5 | 0 | 1 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0005 | 0/0 | 2733 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0006 | 0/0 | 2733 | 6 | 3 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0007 | 0/0 | 2733 | 5 | 0 | 3 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0008 | 0/0 | 2733 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0009 | 0/0 | 2733 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0010 | 0/0 | 2733 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0011 | 0/0 | 2733 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0012 | 0/0 | 2733 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0013 | 0/0 | 2733 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0014 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0015 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0016 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0017 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0018 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0019 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0020 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0021 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0022 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0023 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0024 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
c0025 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2700 | 146 | 12 | 28 | 86 | 4 | 15 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0002 | 0/0 | 2700 | 58 | 14 | 11 | 22 | 3 | 8 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0003 | 0/0 | 2699 | 44 | 10 | 7 | 27 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0004 | 0/0 | 2700 | 32 | 6 | 5 | 14 | 2 | 5 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0005 | 0/0 | 2700 | 21 | 3 | 1 | 15 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0006 | 0/0 | 2699 | 16 | 9 | 1 | 5 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0007 | 0/0 | 2700 | 11 | 4 | 5 | 0 | 1 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0008 | 0/0 | 2700 | 6 | 4 | 1 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0009 | 0/0 | 2700 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0010 | 0/0 | 2700 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0011 | 0/0 | 2700 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0012 | 0/0 | 2700 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0013 | 0/0 | 2700 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0014 | 0/0 | 2699 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0015 | 0/0 | 2700 | 3 | 0 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0016 | 0/0 | 2700 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0017 | 0/1 | 2699 | 2 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0018 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0019 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0020 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0021 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0022 | 0/0 | 2699 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0023 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0024 | 0/0 | 2700 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0025 | 0/0 | 2700 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0026 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0027 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0028 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0029 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0030 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0031 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0032 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0033 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0034 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0035 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0036 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0037 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0038 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0039 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0040 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0041 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0042 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0043 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
t0044 | 0/0 | 2700 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 1 | 6 | 5 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0011 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2733 | 256 | 29 | 44 | 142 | 9 | 31 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0003 | 0/1 | 2733 | 13 | 9 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0006 | 0/0 | 2733 | 6 | 3 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0007 | 0/0 | 2733 | 5 | 0 | 3 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0012 | 0/0 | 2733 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0016 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0017 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002 | 0/0 | 2733 | 76 | 31 | 11 | 33 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0008 | 0/0 | 2733 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0019 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0024 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0025 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0003c0004 | 0/0 | 2733 | 9 | 2 | 5 | 0 | 1 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0004c0005 | 0/0 | 2733 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0005c0009 | 0/0 | 2733 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0006c0010 | 0/0 | 2733 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0007c0011 | 0/0 | 2733 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0008c0013 | 0/0 | 2733 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0009c0015 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0010c0022 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0011c0021 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0012c0020 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0013c0023 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0014c0018 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0015c0014 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5432 | 137 | 6 | 26 | 86 | 4 | 14 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0002 | 0/0 | 5432 | 51 | 14 | 11 | 17 | 3 | 6 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0004 | 0/0 | 5432 | 26 | 2 | 3 | 14 | 2 | 5 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0005 | 0/0 | 5432 | 16 | 1 | 1 | 12 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0007 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0012 | 0/0 | 5432 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0016 | 0/0 | 5432 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0017 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0018 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0024 | 0/0 | 5432 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0027 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0028 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0029 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0030 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0031 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0033 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0035 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0036 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0039 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0040 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0042 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0001t0044 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0003t0001 | 0/0 | 5432 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0003t0004 | 0/0 | 5432 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0003t0017 | 0/1 | 5431 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0003t0022 | 0/0 | 5431 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0003t0023 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0003t0037 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0003t0038 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0006t0001 | 0/0 | 5432 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0006t0004 | 0/0 | 5432 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0007t0015 | 0/0 | 5432 | 3 | 0 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0007t0025 | 0/0 | 5432 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0012t0005 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0016t0004 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0001c0017t0026 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0003 | 0/0 | 5431 | 37 | 5 | 7 | 25 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0006 | 0/0 | 5431 | 12 | 6 | 1 | 4 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0008 | 0/0 | 5432 | 5 | 3 | 1 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0009 | 0/0 | 5432 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0010 | 0/0 | 5432 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0011 | 0/0 | 5432 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0013 | 0/0 | 5432 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0014 | 0/0 | 5431 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0020 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0002t0034 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0008t0003 | 0/0 | 5431 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0008t0006 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0019t0008 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0024t0043 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0002c0025t0032 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0003c0004t0007 | 0/0 | 5432 | 9 | 2 | 5 | 0 | 1 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0004c0005t0002 | 0/0 | 5432 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0004c0005t0005 | 0/0 | 5432 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0005c0009t0006 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0005c0009t0021 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0006c0010t0019 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0006c0010t0041 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0007c0011t0002 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0007c0011t0005 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0008c0013t0003 | 0/0 | 5431 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0009c0015t0001 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0010c0022t0006 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0011c0021t0002 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0012c0020t0003 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0013c0023t0001 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0014c0018t0006 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
a0015c0014t0002 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | copy fasta | chr6 | 46992708 | 47047332 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 12 | 1 | 6 | 5 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0007g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0012g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0012g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0016g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0016g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0016g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0017g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0018g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0018g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0024g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0024g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0027g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0028g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0029g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0030g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0031g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0033g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0035g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0036g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0039g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0040g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0042g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0044g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0017g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0022g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0022g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0023g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0037g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0038g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0007t0015g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0007t0015g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0007t0025g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0007t0025g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0012t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0012t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0016t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0017t0026g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0009g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0010g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0011g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0013g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0013g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0014g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0014g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0020g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0020g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0034g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0008t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0008t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0008t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0008t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0019t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0024t0043g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0025t0032g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0004c0005t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0004c0005t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0004c0005t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0004c0005t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0004c0005t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0005c0009t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0005c0009t0021g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0005c0009t0021g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0006c0010t0019g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0006c0010t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0006c0010t0041g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0007c0011t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0007c0011t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0008c0013t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0009c0015t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0010c0022t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0011c0021t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0012c0020t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0013c0023t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0014c0018t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0015c0014t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0294 | EUR | GBR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00408 | hp2 | a0002 | c0002 | t0003 | g0077 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00558 | hp2 | a0002 | c0002 | t0014 | g0061 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00597 | hp2 | a0002 | c0002 | t0006 | g0249 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00621 | hp2 | a0002 | c0002 | t0003 | g0172 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00639 | hp2 | a0001 | c0006 | t0004 | g0279 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0293 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00642 | hp2 | a0001 | c0006 | t0004 | g0276 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00741 | hp2 | a0002 | c0002 | t0013 | g0160 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0218 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01069 | hp2 | a0001 | c0001 | t0030 | g0114 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0290 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01074 | hp1 | a0001 | c0003 | t0022 | g0309 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01074 | hp2 | a0001 | c0001 | t0031 | g0197 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01106 | hp1 | a0002 | c0024 | t0043 | g0325 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01106 | hp2 | a0001 | c0017 | t0026 | g0214 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01109 | hp2 | a0003 | c0004 | t0007 | g0195 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01168 | hp1 | a0003 | c0004 | t0007 | g0139 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01169 | hp2 | a0003 | c0004 | t0007 | g0138 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01192 | hp1 | a0003 | c0004 | t0007 | g0208 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01192 | hp2 | a0001 | c0001 | t0044 | g0291 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01243 | hp1 | a0002 | c0002 | t0011 | g0132 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01243 | hp2 | a0001 | c0006 | t0001 | g0148 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01255 | hp1 | a0006 | c0010 | t0041 | g0313 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01255 | hp2 | a0003 | c0004 | t0007 | g0219 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0192 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01358 | hp1 | a0002 | c0002 | t0003 | g0047 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0235 | EUR | IBS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0318 | EUR | IBS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01884 | hp1 | a0002 | c0002 | t0010 | g0079 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01884 | hp2 | a0002 | c0002 | t0006 | g0322 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01891 | hp2 | a0005 | c0009 | t0006 | g0331 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01928 | hp1 | a0002 | c0002 | t0003 | g0102 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01928 | hp2 | a0001 | c0003 | t0022 | g0295 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01943 | hp1 | a0002 | c0002 | t0003 | g0051 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01952 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01975 | hp2 | a0001 | c0007 | t0015 | g0018 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01978 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01981 | hp2 | a0001 | c0007 | t0015 | g0018 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02004 | hp1 | a0001 | c0007 | t0015 | g0101 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02004 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02055 | hp1 | a0002 | c0002 | t0003 | g0042 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02056 | hp1 | a0001 | c0001 | t0028 | g0087 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0075 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02074 | hp1 | a0001 | c0001 | t0016 | g0251 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0068 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02132 | hp1 | a0002 | c0002 | t0003 | g0164 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02145 | hp1 | a0001 | c0006 | t0001 | g0110 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02145 | hp2 | a0002 | c0002 | t0009 | g0297 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02148 | hp1 | a0002 | c0002 | t0008 | g0117 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | CDX | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02155 | hp2 | a0002 | c0002 | t0003 | g0194 | EAS | CDX | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02257 | hp1 | a0001 | c0012 | t0005 | g0140 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02257 | hp2 | a0002 | c0008 | t0006 | g0330 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02258 | hp1 | a0002 | c0002 | t0009 | g0037 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0122 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02273 | hp2 | a0002 | c0002 | t0006 | g0257 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02280 | hp1 | a0002 | c0008 | t0003 | g0030 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02300 | hp2 | a0002 | c0002 | t0003 | g0065 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02451 | hp1 | a0005 | c0009 | t0021 | g0329 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02451 | hp2 | a0002 | c0002 | t0006 | g0301 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02572 | hp1 | a0006 | c0010 | t0019 | g0119 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02572 | hp2 | a0002 | c0002 | t0010 | g0007 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02615 | hp1 | a0002 | c0002 | t0009 | g0037 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02622 | hp1 | a0002 | c0002 | t0006 | g0323 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02622 | hp2 | a0002 | c0002 | t0006 | g0321 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02630 | hp1 | a0002 | c0008 | t0003 | g0216 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02630 | hp2 | a0001 | c0003 | t0023 | g0038 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02647 | hp1 | a0001 | c0003 | t0023 | g0038 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02647 | hp2 | a0001 | c0001 | t0027 | g0145 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02683 | hp1 | a0015 | c0014 | t0002 | g0240 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0296 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02717 | hp1 | a0002 | c0002 | t0011 | g0131 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02723 | hp1 | a0001 | c0016 | t0004 | g0302 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02723 | hp2 | a0001 | c0003 | t0004 | g0308 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0292 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02818 | hp1 | a0005 | c0009 | t0021 | g0328 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02896 | hp2 | a0006 | c0010 | t0019 | g0125 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02922 | hp1 | a0013 | c0023 | t0001 | g0111 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02965 | hp1 | a0002 | c0002 | t0020 | g0326 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02970 | hp1 | a0002 | c0002 | t0009 | g0304 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02970 | hp2 | a0002 | c0002 | t0006 | g0320 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02976 | hp1 | a0002 | c0002 | t0009 | g0298 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03017 | hp2 | a0001 | c0001 | t0033 | g0245 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03130 | hp2 | a0012 | c0020 | t0003 | g0149 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03139 | hp1 | a0002 | c0002 | t0008 | g0040 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03195 | hp1 | a0001 | c0003 | t0004 | g0314 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03195 | hp2 | a0001 | c0001 | t0018 | g0215 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03209 | hp1 | a0001 | c0006 | t0001 | g0021 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0044 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03225 | hp2 | a0001 | c0003 | t0037 | g0315 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0319 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03453 | hp1 | a0002 | c0002 | t0003 | g0043 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03453 | hp2 | a0002 | c0019 | t0008 | g0153 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03486 | hp2 | a0002 | c0002 | t0034 | g0312 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03492 | hp2 | a0001 | c0001 | t0042 | g0273 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03516 | hp1 | a0002 | c0002 | t0010 | g0007 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03516 | hp2 | a0003 | c0004 | t0007 | g0159 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03540 | hp1 | a0002 | c0002 | t0011 | g0133 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03540 | hp2 | a0002 | c0002 | t0013 | g0144 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03579 | hp2 | a0002 | c0002 | t0013 | g0078 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03654 | hp2 | a0002 | c0002 | t0006 | g0256 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0317 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0193 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03704 | hp2 | a0003 | c0004 | t0007 | g0221 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0207 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03710 | hp2 | a0011 | c0021 | t0002 | g0282 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0305 | SAS | BEB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | BEB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04115 | hp2 | a0001 | c0001 | t0035 | g0289 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04204 | hp1 | a0009 | c0015 | t0001 | g0222 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0271 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18522 | hp1 | a0002 | c0008 | t0003 | g0217 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18612 | hp2 | a0001 | c0007 | t0025 | g0226 | EAS | CHB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | CHB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18747 | hp2 | a0002 | c0002 | t0008 | g0063 | EAS | CHB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18906 | hp1 | a0003 | c0004 | t0007 | g0158 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18906 | hp2 | a0002 | c0002 | t0006 | g0324 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18941 | hp1 | a0004 | c0005 | t0002 | g0034 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18941 | hp2 | a0001 | c0001 | t0016 | g0223 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18943 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18944 | hp1 | a0001 | c0007 | t0025 | g0227 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18946 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18947 | hp2 | a0002 | c0002 | t0003 | g0060 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18949 | hp1 | a0002 | c0002 | t0003 | g0205 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18953 | hp2 | a0001 | c0001 | t0036 | g0284 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18954 | hp2 | a0002 | c0002 | t0006 | g0033 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18959 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18959 | hp2 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18960 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18965 | hp1 | a0001 | c0001 | t0012 | g0120 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18967 | hp2 | a0008 | c0013 | t0003 | g0022 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18974 | hp2 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18980 | hp1 | a0001 | c0001 | t0012 | g0182 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18980 | hp2 | a0001 | c0001 | t0029 | g0096 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18986 | hp2 | a0014 | c0018 | t0006 | g0281 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0064 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18991 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18991 | hp2 | a0001 | c0001 | t0016 | g0244 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18994 | hp1 | a0007 | c0011 | t0002 | g0270 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18995 | hp2 | a0004 | c0005 | t0002 | g0034 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18997 | hp2 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18998 | hp1 | a0008 | c0013 | t0003 | g0022 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18998 | hp2 | a0004 | c0005 | t0005 | g0200 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18999 | hp1 | a0004 | c0005 | t0002 | g0255 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19003 | hp2 | a0001 | c0001 | t0017 | g0178 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19004 | hp2 | a0004 | c0005 | t0005 | g0073 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19005 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19009 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0206 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19030 | hp1 | a0002 | c0002 | t0003 | g0123 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19030 | hp2 | a0001 | c0001 | t0039 | g0332 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19043 | hp1 | a0002 | c0002 | t0011 | g0045 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19043 | hp2 | a0002 | c0008 | t0003 | g0030 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19060 | hp2 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19067 | hp1 | a0001 | c0001 | t0024 | g0265 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19067 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19074 | hp2 | a0002 | c0002 | t0003 | g0069 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19075 | hp2 | a0004 | c0005 | t0002 | g0262 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19076 | hp1 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19076 | hp2 | a0002 | c0002 | t0006 | g0033 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19077 | hp1 | a0002 | c0002 | t0014 | g0014 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19078 | hp1 | a0007 | c0011 | t0005 | g0152 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19079 | hp2 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19080 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19083 | hp1 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19084 | hp2 | a0002 | c0002 | t0014 | g0014 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19086 | hp1 | a0002 | c0002 | t0006 | g0250 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19087 | hp2 | a0001 | c0001 | t0024 | g0275 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19240 | hp1 | a0001 | c0006 | t0001 | g0021 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19240 | hp2 | a0001 | c0001 | t0018 | g0134 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ASW | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | TSI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0280 | EUR | TSI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20805 | hp1 | a0003 | c0004 | t0007 | g0220 | EUR | TSI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20905 | hp2 | a0001 | c0001 | t0040 | g0272 | SAS | GIH | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02109 | hp1 | a0002 | c0002 | t0020 | g0327 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02109 | hp2 | a0001 | c0003 | t0004 | g0311 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02559 | hp1 | a0001 | c0003 | t0038 | g0310 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03471 | hp1 | a0010 | c0022 | t0006 | g0307 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03471 | hp2 | a0002 | c0025 | t0032 | g0041 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | USA | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG06807 | hp2 | a0002 | c0002 | t0010 | g0007 | AFR | USA | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20300 | hp1 | a0002 | c0002 | t0008 | g0154 | AFR | USA | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA21309 | hp1 | a0002 | c0002 | t0008 | g0112 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA21309 | hp2 | a0001 | c0012 | t0005 | g0141 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0017 | g0198 | REF | REF | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0184 | REF | REF | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47007284
|
A | T | 1 | a0014 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.2501T>A | p.Ile834Asn | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/15 | 2686/5432 | 2501/2733 | 834/910 | chr6 | 47007284 | ||
chr6:47009003
|
A | G | 1 | a0007 | 2 | NA18994.hp1 NA19078.hp1 |
missense_variant | MODERATE | c.2432T>C | p.Ile811Thr | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2617/5432 | 2432/2733 | 811/910 | chr6 | 47009003 | ||
chr6:47009028
|
T | G | 1 | a0006 | 3 | HG01255.hp1 HG02572.hp1 HG02896.hp2 |
missense_variant | MODERATE | c.2407A>C | p.Thr803Pro | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2592/5432 | 2407/2733 | 803/910 | chr6 | 47009028 | ||
chr6:47009076
|
T | C | 5 | a0002a0005a0006others(2): Show | 93 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(90): Show |
missense_variant | MODERATE | c.2359A>G | p.Ile787Val | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2544/5432 | 2359/2733 | 787/910 | chr6 | 47009076 | ||
chr6:47009273
|
G | A | 1 | a0008 | 2 | NA18967.hp2 NA18998.hp1 |
missense_variant | MODERATE | c.2162C>T | p.Thr721Met | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2347/5432 | 2162/2733 | 721/910 | chr6 | 47009273 | ||
chr6:47009722
|
T | C | 6 | a0002a0005a0006others(3): Show | 94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
missense_variant | MODERATE | c.1713A>G | p.Ile571Met | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1898/5432 | 1713/2733 | 571/910 | chr6 | 47009722 | ||
chr6:47009865
|
T | A | 1 | a0010 | 1 | HG03471.hp1 | stop_gained | HIGH | c.1570A>T | p.Lys524* | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1755/5432 | 1570/2733 | 524/910 | chr6 | 47009865 | ||
chr6:47010047
|
C | T | 1 | a0003 | 9 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
missense_variant | MODERATE | c.1388G>A | p.Arg463His | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1573/5432 | 1388/2733 | 463/910 | chr6 | 47010047 | ||
chr6:47010113
|
A | T | 1 | a0004 | 6 | NA18941.hp1 NA18995.hp2 NA18998.hp2 others(3): Show |
missense_variant | MODERATE | c.1322T>A | p.Leu441His | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1507/5432 | 1322/2733 | 441/910 | chr6 | 47010113 | ||
chr6:47010158
|
C | T | 1 | a0005 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.1277G>A | p.Arg426Gln | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1462/5432 | 1277/2733 | 426/910 | chr6 | 47010158 | ||
chr6:47016637
|
G | C | 1 | a0012 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.743C>G | p.Ser248Cys | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/15 | 928/5432 | 743/2733 | 248/910 | chr6 | 47016637 | ||
chr6:47020740
|
G | A | 1 | a0011 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.602C>T | p.Thr201Ile | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/15 | 787/5432 | 602/2733 | 201/910 | chr6 | 47020740 | ||
chr6:47024207
|
G | C | 1 | a0010 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.288C>G | p.Ser96Arg | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/15 | 473/5432 | 288/2733 | 96/910 | chr6 | 47024207 | ||
chr6:47026003
|
C | T | 1 | a0009 | 1 | HG04204.hp1 | missense_variant&splice_region_variant | MODERATE | c.128G>A | p.Gly43Asp | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/15 | 313/5432 | 128/2733 | 43/910 | chr6 | 47026003 | ||
chr6:47027752
|
C | T | 1 | a0015 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.79G>A | p.Gly27Ser | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/15 | 264/5432 | 79/2733 | 27/910 | chr6 | 47027752 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47008954
|
A | G | 1 | a0001c0017 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.2481T>C | p.Asn827Asn | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2666/5432 | 2481/2733 | 827/910 | chr6 | 47008954 | ||
chr6:47008999
|
C | T | 1 | a0001c0016 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.2436G>A | p.Val812Val | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2621/5432 | 2436/2733 | 812/910 | chr6 | 47008999 | ||
chr6:47009188
|
G | A | 1 | a0003c0004 | 9 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
synonymous_variant | LOW | c.2247C>T | p.Val749Val | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2432/5432 | 2247/2733 | 749/910 | chr6 | 47009188 | ||
chr6:47009541
|
G | A | 3 | a0001c0003a0002c0008a0010c0022 | 19 | HG01069.hp1 HG01074.hp1 HG01928.hp2 others(16): Show |
synonymous_variant | LOW | c.1894C>T | p.Leu632Leu | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2079/5432 | 1894/2733 | 632/910 | chr6 | 47009541 | ||
chr6:47009581
|
T | C | 1 | a0001c0012 | 2 | HG02257.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.1854A>G | p.Gln618Gln | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2039/5432 | 1854/2733 | 618/910 | chr6 | 47009581 | ||
chr6:47009739
|
A | G | 1 | a0001c0006 | 6 | HG00639.hp2 HG00642.hp2 HG01243.hp2 others(3): Show |
synonymous_variant | LOW | c.1696T>C | p.Leu566Leu | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1881/5432 | 1696/2733 | 566/910 | chr6 | 47009739 | ||
chr6:47012160
|
T | A | 1 | a0002c0019 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.963A>T | p.Ala321Ala | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/15 | 1148/5432 | 963/2733 | 321/910 | chr6 | 47012160 | ||
chr6:47016648
|
T | C | 1 | a0002c0025 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.732A>G | p.Leu244Leu | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/15 | 917/5432 | 732/2733 | 244/910 | chr6 | 47016648 | ||
chr6:47025917
|
A | G | 1 | a0001c0007 | 5 | HG01975.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
synonymous_variant | LOW | c.214T>C | p.Leu72Leu | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/15 | 399/5432 | 214/2733 | 72/910 | chr6 | 47025917 | ||
chr6:47029014
|
G | A | 3 | a0002c0024a0002c0025a0013c0023 | 3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.48C>T | p.Asp16Asp | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/15 | 233/5432 | 48/2733 | 16/910 | chr6 | 47029014 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46997812
|
CA | C | 13 | a0001c0001t0017a0001c0003t0017a0001c0003t0022others(10): Show | 67 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2409delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2409 | chr6 | 46997812 | |||||
chr6:46997849
|
C | T | 1 | a0002c0025t0032 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2373G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2373 | chr6 | 46997849 | |||||
chr6:46997882
|
T | C | 1 | a0001c0001t0035 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2340A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2340 | chr6 | 46997882 | |||||
chr6:46998102
|
T | C | 1 | a0001c0001t0028 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2120A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2120 | chr6 | 46998102 | |||||
chr6:46998110
|
C | G | 1 | a0005c0009t0021 | 2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2112G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2112 | chr6 | 46998110 | |||||
chr6:46998121
|
C | T | 13 | a0001c0001t0017a0001c0003t0017a0001c0003t0022others(10): Show | 67 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2101G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2101 | chr6 | 46998121 | |||||
chr6:46998156
|
A | C | 2 | a0001c0007t0015a0001c0007t0025 | 5 | HG01975.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2066T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2066 | chr6 | 46998156 | |||||
chr6:46998159
|
A | G | 1 | a0001c0003t0023 | 2 | HG02630.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2063T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2063 | chr6 | 46998159 | |||||
chr6:46998167
|
T | C | 1 | a0002c0025t0032 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2055A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2055 | chr6 | 46998167 | |||||
chr6:46998198
|
G | A | 19 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(16): Show | 108 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2024C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2024 | chr6 | 46998198 | |||||
chr6:46998285
|
C | T | 13 | a0001c0001t0017a0001c0003t0017a0001c0003t0022others(10): Show | 67 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1937G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1937 | chr6 | 46998285 | |||||
chr6:46998301
|
G | A | 1 | a0001c0001t0029 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1921C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1921 | chr6 | 46998301 | |||||
chr6:46998302
|
T | C | 1 | a0001c0003t0038 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1920A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1920 | chr6 | 46998302 | |||||
chr6:46998390
|
C | T | 1 | a0002c0002t0014 | 3 | HG00558.hp2 NA19077.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1832G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1832 | chr6 | 46998390 | |||||
chr6:46998537
|
G | T | 13 | a0001c0001t0017a0001c0003t0017a0001c0003t0022others(10): Show | 67 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1685C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1685 | chr6 | 46998537 | |||||
chr6:46998807
|
G | C | 2 | a0001c0001t0027a0002c0002t0010 | 5 | HG01884.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1415C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1415 | chr6 | 46998807 | |||||
chr6:46998809
|
G | A | 1 | a0001c0001t0039 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1413C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1413 | chr6 | 46998809 | |||||
chr6:46998924
|
G | A | 1 | a0001c0001t0030 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1298C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1298 | chr6 | 46998924 | |||||
chr6:46998945
|
A | G | 4 | a0002c0002t0009a0002c0002t0013a0006c0010t0019others(1): Show | 11 | HG00741.hp2 HG01255.hp1 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1277T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1277 | chr6 | 46998945 | |||||
chr6:46998950
|
T | C | 1 | a0001c0001t0040 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1272A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1272 | chr6 | 46998950 | |||||
chr6:46998969
|
C | T | 1 | a0002c0002t0020 | 2 | HG02109.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1253G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1253 | chr6 | 46998969 | |||||
chr6:46999047
|
G | A | 1 | a0001c0001t0035 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1175C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1175 | chr6 | 46999047 | |||||
chr6:46999079
|
C | A | 1 | a0002c0002t0013 | 3 | HG00741.hp2 HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1143G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1143 | chr6 | 46999079 | |||||
chr6:46999156
|
G | A | 1 | a0001c0001t0031 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1066C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1066 | chr6 | 46999156 | |||||
chr6:46999175
|
T | C | 1 | a0001c0001t0018 | 2 | HG03195.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1047A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1047 | chr6 | 46999175 | |||||
chr6:46999377
|
G | A | 1 | a0005c0009t0021 | 2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*845C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 845 | chr6 | 46999377 | |||||
chr6:46999448
|
C | T | 1 | a0001c0003t0037 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*774G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 774 | chr6 | 46999448 | |||||
chr6:46999556
|
C | G | 15 | a0001c0001t0002a0001c0001t0005a0001c0001t0018others(12): Show | 91 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*666G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 666 | chr6 | 46999556 | |||||
chr6:46999601
|
C | T | 15 | a0002c0002t0003a0002c0002t0006a0002c0002t0008others(12): Show | 76 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*621G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 621 | chr6 | 46999601 | |||||
chr6:46999640
|
G | A | 20 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(17): Show | 105 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*582C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 582 | chr6 | 46999640 | |||||
chr6:46999716
|
C | T | 1 | a0001c0001t0036 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 506 | chr6 | 46999716 | |||||
chr6:46999804
|
C | G | 23 | a0001c0001t0027a0001c0001t0035a0002c0002t0003others(20): Show | 94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*418G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 418 | chr6 | 46999804 | |||||
chr6:47000041
|
C | T | 2 | a0002c0002t0009a0002c0002t0013 | 8 | HG00741.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*181G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 181 | chr6 | 47000041 | |||||
chr6:47000148
|
A | C | 1 | a0001c0017t0026 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 74 | chr6 | 47000148 | |||||
chr6:47000168
|
C | T | 1 | a0001c0001t0033 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*54G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 54 | chr6 | 47000168 | |||||
chr6:47029082
|
G | A | 2 | a0002c0024t0043a0002c0025t0032 | 2 | HG01106.hp1 HG03471.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-21C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/15 | chr6 | 47029082 | ||||||
chr6:47029098
|
T | C | 1 | a0001c0001t0044 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/15 | 37 | chr6 | 47029098 | |||||
chr6:47042215
|
G | C | 34 | a0001c0001t0002a0001c0001t0004a0001c0001t0016others(31): Show | 138 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(135): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/15 | chr6 | 47042215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47000370
|
C | A | 2 | a0001c0001t0005g0070a0001c0001t0005g0071 | 2 | NA18948.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2660-75G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47000370 | ||||||
chr6:47000431
|
C | T | 157 | a0001c0001t0001g0056a0001c0001t0001g0202a0001c0001t0002g0005others(154): Show | 184 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.2660-136G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47000431 | ||||||
chr6:47000701
|
C | T | 1 | a0002c0002t0003g0076 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2660-406G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47000701 | ||||||
chr6:47000901
|
TC | T | 66 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(63): Show | 81 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2659+599delG | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47000901 | ||||||
chr6:47001301
|
G | T | 93 | a0001c0001t0001g0056a0001c0001t0001g0202a0001c0001t0002g0005others(90): Show | 106 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2659+200C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47001301 | ||||||
chr6:47001723
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2593-156A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47001723 | ||||||
chr6:47001888
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2593-321T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47001888 | ||||||
chr6:47002090
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2593-523T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002090 | ||||||
chr6:47002096
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2593-529G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002096 | ||||||
chr6:47002309
|
G | T | 4 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2593-742C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002309 | ||||||
chr6:47002383
|
G | GA | 7 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2593-817dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002383 | ||||||
chr6:47002399
|
A | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0161 | 7 | NA18949.hp2 NA18961.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.2593-832T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002399 | ||||||
chr6:47002488
|
A | C | 168 | a0001c0001t0001g0056a0001c0001t0001g0202a0001c0001t0002g0005others(165): Show | 196 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.2593-921T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002488 | ||||||
chr6:47002582
|
T | C | 4 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2593-1015A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002582 | ||||||
chr6:47002635
|
A | G | 1 | a0015c0014t0002g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2593-1068T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002635 | ||||||
chr6:47002747
|
A | T | 71 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(68): Show | 86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.2593-1180T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002747 | ||||||
chr6:47002790
|
G | A | 14 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(11): Show | 22 | HG01358.hp1 HG01928.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.2593-1223C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002790 | ||||||
chr6:47002837
|
T | C | 1 | a0001c0001t0031g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2593-1270A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002837 | ||||||
chr6:47002858
|
G | C | 1 | a0002c0002t0014g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2593-1291C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002858 | ||||||
chr6:47002949
|
C | T | 4 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2593-1382G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002949 | ||||||
chr6:47002998
|
A | G | 2 | a0001c0001t0004g0224a0001c0001t0004g0247 | 2 | HG02155.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2593-1431T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002998 | ||||||
chr6:47003011
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2593-1444C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003011 | ||||||
chr6:47003695
|
A | G | 1 | a0003c0004t0007g0220 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2592+2122T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003695 | ||||||
chr6:47003724
|
C | T | 1 | a0001c0003t0004g0311 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2592+2093G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003724 | ||||||
chr6:47003828
|
G | A | 1 | a0001c0003t0037g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2592+1989C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003828 | ||||||
chr6:47003875
|
A | G | 3 | a0005c0009t0006g0331a0005c0009t0021g0328a0005c0009t0021g0329 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2592+1942T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003875 | ||||||
chr6:47004168
|
C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0177a0001c0001t0004g0248 | 3 | HG00544.hp1 NA18955.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2592+1649G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004168 | ||||||
chr6:47004169
|
G | A | 1 | a0011c0021t0002g0282 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2592+1648C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004169 | ||||||
chr6:47004409
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2592+1408A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004409 | ||||||
chr6:47004434
|
A | T | 58 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(55): Show | 72 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.2592+1383T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004434 | ||||||
chr6:47004483
|
T | C | 75 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(72): Show | 90 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.2592+1334A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004483 | ||||||
chr6:47004507
|
T | C | 1 | a0002c0025t0032g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2592+1310A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004507 | ||||||
chr6:47004707
|
C | T | 1 | a0001c0017t0026g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2592+1110G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004707 | ||||||
chr6:47004731
|
C | T | 1 | a0001c0001t0001g0020 | 2 | NA18951.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2592+1086G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004731 | ||||||
chr6:47004917
|
G | A | 1 | a0001c0007t0025g0227 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2592+900C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004917 | ||||||
chr6:47004930
|
G | C | 1 | a0001c0001t0001g0170 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2592+887C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004930 | ||||||
chr6:47004964
|
C | T | 168 | a0001c0001t0001g0056a0001c0001t0001g0202a0001c0001t0002g0005others(165): Show | 196 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.2592+853G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004964 | ||||||
chr6:47004966
|
T | G | 1 | a0001c0001t0004g0280 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2592+851A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004966 | ||||||
chr6:47005060
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0092 | 5 | NA18955.hp2 NA18986.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2592+757A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005060 | ||||||
chr6:47005165
|
T | C | 1 | a0002c0002t0006g0324 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2592+652A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005165 | ||||||
chr6:47005217
|
C | T | 4 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2592+600G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005217 | ||||||
chr6:47005317
|
C | A | 7 | a0001c0001t0002g0266a0001c0001t0002g0268a0001c0001t0002g0285others(4): Show | 7 | HG00609.hp1 HG02056.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.2592+500G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005317 | ||||||
chr6:47005344
|
A | G | 1 | a0001c0003t0001g0218 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2592+473T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005344 | ||||||
chr6:47005507
|
T | C | 1 | a0003c0004t0007g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2592+310A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005507 | ||||||
chr6:47005569
|
A | T | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2592+248T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005569 | ||||||
chr6:47005727
|
C | T | 1 | a0001c0001t0004g0232 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2592+90G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005727 | ||||||
chr6:47005935
|
C | G | 1 | a0002c0025t0032g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2533-59G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47005935 | ||||||
chr6:47005946
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2533-70C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47005946 | ||||||
chr6:47005972
|
A | G | 3 | a0005c0009t0006g0331a0005c0009t0021g0328a0005c0009t0021g0329 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2533-96T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47005972 | ||||||
chr6:47006177
|
A | G | 3 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133 | 3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2533-301T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006177 | ||||||
chr6:47006415
|
A | T | 1 | a0002c0002t0006g0321 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2533-539T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006415 | ||||||
chr6:47006461
|
AATTTT | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 202 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.2533-590_2533-586d others(7): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006461 | ||||||
chr6:47006552
|
T | C | 3 | a0001c0003t0017g0198a0001c0003t0022g0295a0001c0003t0022g0309 | 3 | HG01074.hp1 HG01928.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2533-676A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006552 | ||||||
chr6:47006690
|
C | T | 1 | a0002c0025t0032g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2532+563G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006690 | ||||||
chr6:47006820
|
C | T | 1 | a0004c0005t0005g0200 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2532+433G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006820 | ||||||
chr6:47006833
|
T | C | 5 | a0004c0005t0002g0034a0004c0005t0002g0255a0004c0005t0002g0262others(2): Show | 6 | NA18941.hp1 NA18995.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.2532+420A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006833 | ||||||
chr6:47007034
|
TTTACA | T | 3 | a0002c0002t0013g0078a0002c0002t0013g0144a0002c0002t0013g0160 | 3 | HG00741.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2532+214_2532+218d others(7): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47007034 | ||||||
chr6:47007040
|
T | G | 1 | a0001c0001t0039g0332 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2532+213A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47007040 | ||||||
chr6:47007076
|
G | T | 69 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(66): Show | 84 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2532+177C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47007076 | ||||||
chr6:47007383
|
A | G | 4 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-89T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007383 | ||||||
chr6:47007422
|
G | T | 3 | a0005c0009t0006g0331a0005c0009t0021g0328a0005c0009t0021g0329 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2491-128C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007422 | ||||||
chr6:47007423
|
T | A | 3 | a0005c0009t0006g0331a0005c0009t0021g0328a0005c0009t0021g0329 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2491-129A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007423 | ||||||
chr6:47007424
|
A | AGAGACT | 3 | a0005c0009t0006g0331a0005c0009t0021g0328a0005c0009t0021g0329 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2491-131_2491-130i others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007424 | ||||||
chr6:47007429
|
C | CCTTAAGA others(2): Show |
3 | a0005c0009t0006g0331a0005c0009t0021g0328a0005c0009t0021g0329 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2491-136_2491-135i others(11): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007429 | ||||||
chr6:47007530
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2491-236G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007530 | ||||||
chr6:47007659
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 103 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.2491-365G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007659 | ||||||
chr6:47007761
|
T | C | 1 | a0001c0007t0025g0226 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2491-467A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007761 | ||||||
chr6:47007957
|
A | G | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2491-663T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007957 | ||||||
chr6:47007978
|
A | G | 4 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-684T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007978 | ||||||
chr6:47008162
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2490+783G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008162 | ||||||
chr6:47008429
|
G | A | 2 | a0002c0002t0020g0326a0002c0002t0020g0327 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2490+516C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008429 | ||||||
chr6:47008658
|
A | G | 7 | a0002c0002t0008g0040a0002c0002t0008g0154a0002c0002t0011g0045others(4): Show | 7 | HG01243.hp1 HG02717.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2490+287T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008658 | ||||||
chr6:47008672
|
T | C | 3 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133 | 3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2490+273A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008672 | ||||||
chr6:47008833
|
G | A | 2 | a0001c0001t0018g0134a0001c0001t0018g0215 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2490+112C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008833 | ||||||
chr6:47008900
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0004g0238 | 2 | NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2490+45A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008900 | ||||||
chr6:47010639
|
C | T | 27 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044others(24): Show | 30 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1117-321G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010639 | ||||||
chr6:47010973
|
G | GCAGAGTG others(1): Show |
5 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-656_1117-655i others(10): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010973 | ||||||
chr6:47010976
|
C | G | 5 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-658G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010976 | ||||||
chr6:47010977
|
C | G | 5 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-659G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010977 | ||||||
chr6:47010983
|
A | G | 1 | a0001c0016t0004g0302 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1117-665T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010983 | ||||||
chr6:47011132
|
A | T | 68 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(65): Show | 83 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1117-814T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47011132 | ||||||
chr6:47011149
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1117-831A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47011149 | ||||||
chr6:47011432
|
T | A | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1116+575A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47011432 | ||||||
chr6:47011667
|
T | C | 70 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(67): Show | 85 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1116+340A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47011667 | ||||||
chr6:47012203
|
C | T | 3 | a0005c0009t0006g0331a0005c0009t0021g0328a0005c0009t0021g0329 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
splice_region_variant&intron_variant | LOW | c.928-8G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012203 | ||||||
chr6:47012204
|
G | A | 1 | a0002c0025t0032g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.928-9C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012204 | ||||||
chr6:47012379
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 295 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(292): Show |
intron_variant | MODIFIER | c.928-184C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012379 | ||||||
chr6:47012416
|
C | G | 1 | a0012c0020t0003g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.928-221G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012416 | ||||||
chr6:47012611
|
G | A | 1 | a0005c0009t0021g0328 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.928-416C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012611 | ||||||
chr6:47012622
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 202 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.928-427C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012622 | ||||||
chr6:47012688
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.928-493C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012688 | ||||||
chr6:47012721
|
G | A | 2 | a0001c0001t0018g0134a0001c0001t0018g0215 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.928-526C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012721 | ||||||
chr6:47012753
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0012g0025 | 5 | NA18964.hp1 NA18974.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-558C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012753 | ||||||
chr6:47012798
|
C | T | 1 | a0002c0002t0003g0205 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.928-603G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012798 | ||||||
chr6:47012911
|
C | T | 1 | a0001c0001t0044g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.928-716G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012911 | ||||||
chr6:47013013
|
C | T | 1 | a0002c0025t0032g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.928-818G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013013 | ||||||
chr6:47013067
|
C | T | 1 | a0001c0006t0001g0148 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.928-872G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013067 | ||||||
chr6:47013124
|
C | A | 4 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-929G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013124 | ||||||
chr6:47013190
|
C | T | 2 | a0002c0002t0011g0132a0002c0002t0011g0133 | 2 | HG01243.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.928-995G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013190 | ||||||
chr6:47013202
|
C | T | 5 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-1007G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013202 | ||||||
chr6:47013218
|
G | A | 1 | a0002c0002t0034g0312 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.928-1023C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013218 | ||||||
chr6:47013253
|
G | T | 3 | a0005c0009t0006g0331a0005c0009t0021g0328a0005c0009t0021g0329 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.928-1058C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013253 | ||||||
chr6:47013353
|
C | A | 1 | a0001c0001t0002g0263 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.928-1158G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013353 | ||||||
chr6:47013719
|
A | G | 1 | a0002c0002t0008g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.927+962T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013719 | ||||||
chr6:47013759
|
G | C | 1 | a0001c0001t0004g0305 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.927+922C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013759 | ||||||
chr6:47013878
|
T | TTC | 14 | a0001c0001t0001g0113a0001c0001t0002g0228a0001c0001t0002g0239others(11): Show | 15 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.927+801_927+802dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013878 | ||||||
chr6:47013878
|
TTC | T | 73 | a0001c0001t0005g0193a0002c0002t0003g0004a0002c0002t0003g0006others(70): Show | 88 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.927+801_927+802del others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013878 | ||||||
chr6:47013939
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0181 | 8 | NA18949.hp2 NA18961.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+742G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013939 | ||||||
chr6:47013947
|
A | G | 5 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+734T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013947 | ||||||
chr6:47014056
|
T | C | 23 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044others(20): Show | 26 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.927+625A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014056 | ||||||
chr6:47014114
|
C | G | 1 | a0001c0001t0001g0213 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.927+567G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014114 | ||||||
chr6:47014218
|
A | C | 2 | a0001c0001t0002g0294a0001c0001t0005g0192 | 2 | HG00099.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.927+463T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014218 | ||||||
chr6:47014259
|
C | T | 5 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+422G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014259 | ||||||
chr6:47014539
|
G | A | 5 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+142C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014539 | ||||||
chr6:47014607
|
T | C | 1 | a0002c0002t0008g0063 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.927+74A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014607 | ||||||
chr6:47014611
|
C | T | 6 | a0002c0002t0008g0040a0002c0002t0008g0112a0002c0002t0008g0154others(3): Show | 8 | HG01884.hp1 HG02572.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+70G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014611 | ||||||
chr6:47014866
|
A | G | 6 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-22T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47014866 | ||||||
chr6:47014892
|
G | T | 5 | a0001c0001t0018g0134a0001c0001t0018g0215a0005c0009t0006g0331others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-48C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47014892 | ||||||
chr6:47014924
|
A | C | 5 | a0001c0001t0018g0134a0001c0001t0018g0215a0005c0009t0006g0331others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-80T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47014924 | ||||||
chr6:47014987
|
T | C | 1 | a0001c0001t0005g0211 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.764-143A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47014987 | ||||||
chr6:47015045
|
C | T | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.764-201G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015045 | ||||||
chr6:47015073
|
T | G | 83 | a0001c0001t0001g0056a0001c0001t0001g0082a0001c0001t0001g0083others(80): Show | 95 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.764-229A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015073 | ||||||
chr6:47015218
|
A | G | 30 | a0002c0002t0003g0004a0002c0002t0003g0006a0002c0002t0003g0015others(27): Show | 40 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.764-374T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015218 | ||||||
chr6:47015236
|
G | T | 6 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0204others(3): Show | 6 | HG01070.hp1 HG01261.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-392C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015236 | ||||||
chr6:47015415
|
A | AT | 70 | a0001c0001t0001g0048a0001c0001t0001g0089a0001c0001t0001g0118others(67): Show | 84 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.764-572dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015415 | ||||||
chr6:47015415
|
AT | A | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0090others(3): Show | 6 | NA18947.hp1 NA18963.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-572delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015415 | ||||||
chr6:47015420
|
T | TA | 4 | a0002c0002t0009g0037a0002c0002t0009g0297a0002c0002t0009g0298others(1): Show | 5 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-577_764-576ins others(1): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015420 | ||||||
chr6:47015519
|
A | T | 174 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0118others(171): Show | 203 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(200): Show |
intron_variant | MODIFIER | c.764-675T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015519 | ||||||
chr6:47015573
|
G | A | 3 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044 | 3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.764-729C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015573 | ||||||
chr6:47015574
|
C | CTATT | 5 | a0001c0001t0002g0268a0001c0001t0031g0197a0002c0002t0006g0256others(2): Show | 5 | HG01074.hp2 HG03471.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.764-734_764-731dup others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | ||||||
chr6:47015574
|
C | CTATTTAT others(5): Show |
50 | a0001c0001t0001g0048a0001c0001t0001g0118a0001c0001t0004g0248others(47): Show | 58 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.764-742_764-731dup others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | ||||||
chr6:47015574
|
C | CTATTTAT others(9): Show |
17 | a0002c0002t0003g0004a0002c0002t0003g0019a0002c0002t0003g0064others(14): Show | 23 | HG00741.hp2 HG01255.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.764-746_764-731dup others(16): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | ||||||
chr6:47015574
|
C | CTATTTAT others(13): Show |
2 | a0002c0002t0003g0015a0002c0002t0003g0060 | 3 | NA18947.hp2 NA18959.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.764-750_764-731dup others(20): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | ||||||
chr6:47015574
|
CTATT | C | 6 | a0002c0002t0011g0045a0002c0002t0011g0131a0002c0002t0011g0132others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-734_764-731del others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | ||||||
chr6:47015610
|
C | A | 2 | a0002c0002t0034g0312a0002c0025t0032g0041 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.764-766G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015610 | ||||||
chr6:47015661
|
C | T | 5 | a0004c0005t0002g0034a0004c0005t0002g0255a0004c0005t0002g0262others(2): Show | 6 | NA18941.hp1 NA18995.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-817G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015661 | ||||||
chr6:47015671
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.764-827A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015671 | ||||||
chr6:47015691
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.764-847C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015691 | ||||||
chr6:47015702
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.764-858G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015702 | ||||||
chr6:47015732
|
T | C | 1 | a0002c0002t0034g0312 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.763+885A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015732 | ||||||
chr6:47015734
|
T | C | 16 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(13): Show | 17 | HG01106.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.763+883A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015734 | ||||||
chr6:47015746
|
C | T | 15 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0002t0003g0042others(12): Show | 17 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.763+871G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015746 | ||||||
chr6:47015754
|
AT | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 308 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.763+862delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015754 | ||||||
chr6:47015786
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.763+831G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015786 | ||||||
chr6:47015806
|
C | T | 10 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(7): Show | 11 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.763+811G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015806 | ||||||
chr6:47015939
|
C | T | 15 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(12): Show | 16 | HG01106.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.763+678G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015939 | ||||||
chr6:47015974
|
G | T | 2 | a0001c0001t0002g0225a0001c0001t0002g0230 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.763+643C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015974 | ||||||
chr6:47015991
|
G | A | 1 | a0001c0001t0004g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.763+626C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015991 | ||||||
chr6:47016018
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.763+599C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016018 | ||||||
chr6:47016027
|
T | C | 176 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0115others(173): Show | 205 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.763+590A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016027 | ||||||
chr6:47016197
|
A | G | 2 | a0001c0012t0005g0140a0001c0012t0005g0141 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.763+420T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016197 | ||||||
chr6:47016214
|
T | TTG | 14 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0002t0003g0043others(11): Show | 16 | HG01255.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.763+401_763+402dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016214 | ||||||
chr6:47016272
|
C | A | 1 | a0001c0001t0005g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.763+345G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016272 | ||||||
chr6:47016352
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.763+265G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016352 | ||||||
chr6:47016363
|
G | A | 3 | a0001c0003t0001g0142a0001c0003t0001g0143a0006c0010t0019g0119 | 3 | HG02572.hp1 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.763+254C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016363 | ||||||
chr6:47016487
|
G | A | 3 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133 | 3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.763+130C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016487 | ||||||
chr6:47016529
|
C | T | 2 | a0002c0002t0020g0326a0002c0002t0020g0327 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.763+88G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016529 | ||||||
chr6:47016539
|
C | T | 1 | a0002c0002t0011g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.763+78G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016539 | ||||||
chr6:47016827
|
C | G | 5 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133others(2): Show | 5 | HG01106.hp1 HG01243.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-59G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016827 | ||||||
chr6:47016828
|
G | A | 1 | a0001c0001t0031g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.612-60C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016828 | ||||||
chr6:47016852
|
T | C | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.612-84A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016852 | ||||||
chr6:47016937
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.612-169T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016937 | ||||||
chr6:47016949
|
G | GAT | 3 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133 | 3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.612-183_612-182dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016949 | ||||||
chr6:47016971
|
C | T | 9 | a0001c0003t0004g0308a0001c0003t0004g0311a0001c0003t0004g0314others(6): Show | 10 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.612-203G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016971 | ||||||
chr6:47017084
|
A | G | 1 | a0001c0001t0002g0294 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.612-316T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017084 | ||||||
chr6:47017150
|
C | T | 4 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.612-382G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017150 | ||||||
chr6:47017151
|
G | C | 1 | a0001c0001t0002g0294 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.612-383C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017151 | ||||||
chr6:47017157
|
A | T | 1 | a0001c0001t0002g0294 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.612-389T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017157 | ||||||
chr6:47017194
|
T | C | 1 | a0002c0002t0011g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.612-426A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017194 | ||||||
chr6:47017320
|
G | A | 18 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0204others(15): Show | 19 | HG01070.hp1 HG01261.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.612-552C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017320 | ||||||
chr6:47017353
|
C | T | 1 | a0001c0001t0004g0319 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.612-585G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017353 | ||||||
chr6:47017490
|
A | G | 1 | a0005c0009t0006g0331 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.612-722T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017490 | ||||||
chr6:47017685
|
G | A | 1 | a0001c0001t0005g0193 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.612-917C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017685 | ||||||
chr6:47017690
|
T | A | 10 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044others(7): Show | 12 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.612-922A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017690 | ||||||
chr6:47017692
|
C | CA | 18 | a0001c0001t0001g0091a0001c0001t0001g0185a0001c0001t0002g0258others(15): Show | 18 | HG00099.hp1 HG01175.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.612-925dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017692 | ||||||
chr6:47017692
|
CA | C | 61 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(58): Show | 77 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.612-925delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017692 | ||||||
chr6:47017791
|
C | T | 175 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0115others(172): Show | 204 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(201): Show |
intron_variant | MODIFIER | c.612-1023G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017791 | ||||||
chr6:47017852
|
G | A | 7 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.612-1084C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017852 | ||||||
chr6:47017947
|
A | T | 1 | a0001c0006t0001g0148 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.612-1179T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017947 | ||||||
chr6:47018219
|
C | T | 86 | a0001c0001t0001g0056a0001c0001t0001g0156a0001c0001t0001g0157others(83): Show | 99 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.612-1451G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018219 | ||||||
chr6:47018453
|
C | G | 1 | a0015c0014t0002g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.612-1685G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018453 | ||||||
chr6:47018511
|
C | A | 9 | a0001c0003t0004g0308a0001c0003t0004g0311a0001c0003t0004g0314others(6): Show | 10 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.612-1743G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018511 | ||||||
chr6:47018643
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.612-1875C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018643 | ||||||
chr6:47018674
|
G | A | 1 | a0001c0001t0002g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.612-1906C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018674 | ||||||
chr6:47018681
|
G | C | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.612-1913C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018681 | ||||||
chr6:47018705
|
A | C | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.612-1937T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018705 | ||||||
chr6:47018710
|
A | G | 2 | a0002c0024t0043g0325a0013c0023t0001g0111 | 2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.612-1942T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018710 | ||||||
chr6:47018766
|
T | A | 2 | a0002c0024t0043g0325a0013c0023t0001g0111 | 2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+1965A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018766 | ||||||
chr6:47018770
|
A | G | 96 | a0001c0001t0001g0056a0001c0001t0001g0156a0001c0001t0001g0157others(93): Show | 109 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.611+1961T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018770 | ||||||
chr6:47018834
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02135.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.611+1897G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018834 | ||||||
chr6:47018880
|
G | T | 5 | a0001c0001t0001g0162a0001c0001t0001g0179a0001c0001t0001g0187others(2): Show | 5 | HG01943.hp1 NA18960.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.611+1851C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018880 | ||||||
chr6:47018970
|
A | G | 96 | a0001c0001t0001g0056a0001c0001t0001g0156a0001c0001t0001g0157others(93): Show | 109 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.611+1761T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018970 | ||||||
chr6:47019028
|
C | T | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.611+1703G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019028 | ||||||
chr6:47019045
|
G | A | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+1686C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019045 | ||||||
chr6:47019101
|
A | C | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+1630T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019101 | ||||||
chr6:47019180
|
G | A | 283 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(280): Show | 331 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(328): Show |
intron_variant | MODIFIER | c.611+1551C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019180 | ||||||
chr6:47019384
|
G | A | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+1347C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019384 | ||||||
chr6:47019468
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.611+1263C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019468 | ||||||
chr6:47019499
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.611+1232G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019499 | ||||||
chr6:47019561
|
G | A | 1 | a0002c0002t0006g0249 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.611+1170C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019561 | ||||||
chr6:47019576
|
C | G | 1 | a0001c0001t0004g0252 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.611+1155G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019576 | ||||||
chr6:47019595
|
G | A | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.611+1136C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019595 | ||||||
chr6:47019617
|
G | A | 4 | a0001c0001t0002g0031a0001c0001t0002g0228a0001c0001t0002g0229others(1): Show | 5 | HG01081.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.611+1114C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019617 | ||||||
chr6:47019631
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.611+1100G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019631 | ||||||
chr6:47019633
|
G | A | 2 | a0002c0024t0043g0325a0013c0023t0001g0111 | 2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+1098C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019633 | ||||||
chr6:47019648
|
C | T | 54 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(51): Show | 68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.611+1083G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019648 | ||||||
chr6:47019663
|
G | A | 2 | a0002c0002t0020g0326a0002c0002t0020g0327 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.611+1068C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019663 | ||||||
chr6:47019683
|
C | CAA | 8 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0008t0006g0330others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.611+1046_611+1047d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019683 | ||||||
chr6:47019683
|
CA | C | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 371 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.611+1047delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019683 | ||||||
chr6:47019802
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.611+929T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019802 | ||||||
chr6:47019897
|
A | G | 8 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0204others(5): Show | 8 | HG01070.hp1 HG01261.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.611+834T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019897 | ||||||
chr6:47020025
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0202 | 2 | NA18970.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.611+706C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020025 | ||||||
chr6:47020027
|
A | G | 2 | a0002c0024t0043g0325a0013c0023t0001g0111 | 2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+704T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020027 | ||||||
chr6:47020054
|
C | T | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.611+677G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020054 | ||||||
chr6:47020089
|
T | C | 2 | a0001c0001t0002g0035a0001c0001t0002g0288 | 3 | NA18984.hp2 NA19060.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.611+642A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020089 | ||||||
chr6:47020174
|
C | T | 9 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.611+557G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020174 | ||||||
chr6:47020248
|
C | T | 1 | a0001c0001t0039g0332 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.611+483G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020248 | ||||||
chr6:47020258
|
C | T | 2 | a0001c0007t0025g0226a0002c0002t0003g0047 | 2 | HG01358.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.611+473G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020258 | ||||||
chr6:47020292
|
A | G | 5 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0054others(2): Show | 5 | HG00408.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.611+439T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020292 | ||||||
chr6:47020307
|
A | G | 1 | a0001c0001t0033g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.611+424T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020307 | ||||||
chr6:47020324
|
C | T | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+407G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020324 | ||||||
chr6:47020329
|
C | G | 43 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(40): Show | 55 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.611+402G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020329 | ||||||
chr6:47020362
|
G | A | 2 | a0002c0024t0043g0325a0013c0023t0001g0111 | 2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+369C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020362 | ||||||
chr6:47020370
|
T | C | 176 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0115others(173): Show | 205 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.611+361A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020370 | ||||||
chr6:47020390
|
G | A | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+341C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020390 | ||||||
chr6:47020482
|
C | T | 1 | a0001c0003t0037g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.611+249G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020482 | ||||||
chr6:47020502
|
C | CA | 64 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(61): Show | 80 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.611+228dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020502 | ||||||
chr6:47020502
|
C | CAA | 8 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.611+227_611+228dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020502 | ||||||
chr6:47020502
|
C | CAAA | 8 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.611+226_611+228dup others(3): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020502 | ||||||
chr6:47020609
|
C | T | 3 | a0001c0001t0016g0223a0001c0001t0016g0244a0001c0001t0016g0251 | 3 | HG02074.hp1 NA18941.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.611+122G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020609 | ||||||
chr6:47020612
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.611+119T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020612 | ||||||
chr6:47020809
|
A | G | 2 | a0001c0001t0018g0134a0001c0001t0018g0215 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.553-20T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47020809 | ||||||
chr6:47020860
|
T | C | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.553-71A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47020860 | ||||||
chr6:47020912
|
C | T | 176 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0115others(173): Show | 205 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.553-123G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47020912 | ||||||
chr6:47021052
|
G | A | 2 | a0002c0002t0020g0326a0002c0002t0020g0327 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.553-263C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021052 | ||||||
chr6:47021085
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.553-296C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021085 | ||||||
chr6:47021362
|
A | AT | 12 | a0001c0001t0001g0168a0001c0003t0001g0218a0003c0004t0007g0138others(9): Show | 12 | HG01069.hp1 HG01109.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-574dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021362 | ||||||
chr6:47021362
|
A | ATTTTTTT others(524): Show |
1 | a0001c0003t0004g0308 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.553-574_553-573ins others(531): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021362 | ||||||
chr6:47021400
|
A | G | 80 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(77): Show | 96 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.552+558T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021400 | ||||||
chr6:47021657
|
G | A | 3 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133 | 3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.552+301C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021657 | ||||||
chr6:47021793
|
G | A | 39 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(36): Show | 50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.552+165C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021793 | ||||||
chr6:47021838
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.552+120C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021838 | ||||||
chr6:47021858
|
G | A | 39 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(36): Show | 50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.552+100C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021858 | ||||||
chr6:47021925
|
C | T | 1 | a0001c0001t0028g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.552+33G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021925 | ||||||
chr6:47021943
|
G | A | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.552+15C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021943 | ||||||
chr6:47022092
|
T | A | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.452-34A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022092 | ||||||
chr6:47022112
|
C | T | 66 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(63): Show | 81 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.452-54G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022112 | ||||||
chr6:47022153
|
A | G | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.452-95T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022153 | ||||||
chr6:47022804
|
C | CT | 79 | a0001c0001t0001g0127a0001c0001t0001g0156a0001c0001t0001g0157others(76): Show | 91 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.452-747dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022804 | ||||||
chr6:47022804
|
C | CTT | 12 | a0001c0003t0001g0218a0002c0008t0006g0330a0003c0004t0007g0138others(9): Show | 12 | HG01069.hp1 HG01109.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-748_452-747dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022804 | ||||||
chr6:47022804
|
C | T | 1 | a0002c0008t0003g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.452-746G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022804 | ||||||
chr6:47022804
|
CT | C | 20 | a0001c0001t0001g0171a0002c0002t0003g0042a0002c0002t0003g0043others(17): Show | 23 | HG00621.hp2 HG00741.hp2 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.452-747delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022804 | ||||||
chr6:47022809
|
T | C | 1 | a0002c0002t0011g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.452-751A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022809 | ||||||
chr6:47022837
|
C | T | 1 | a0006c0010t0041g0313 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.452-779G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022837 | ||||||
chr6:47022888
|
C | G | 4 | a0002c0008t0006g0330a0005c0009t0006g0331a0005c0009t0021g0328others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-830G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022888 | ||||||
chr6:47022957
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.452-899G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022957 | ||||||
chr6:47022973
|
A | G | 8 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0008t0006g0330others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-915T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022973 | ||||||
chr6:47023010
|
C | G | 1 | a0001c0001t0001g0213 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.452-952G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023010 | ||||||
chr6:47023062
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.451+982C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023062 | ||||||
chr6:47023124
|
T | C | 2 | a0002c0024t0043g0325a0013c0023t0001g0111 | 2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.451+920A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023124 | ||||||
chr6:47023218
|
C | A | 2 | a0006c0010t0019g0125a0006c0010t0041g0313 | 2 | HG01255.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.451+826G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023218 | ||||||
chr6:47023288
|
G | A | 8 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0008t0006g0330others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.451+756C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023288 | ||||||
chr6:47023312
|
T | C | 1 | a0001c0001t0005g0199 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.451+732A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023312 | ||||||
chr6:47023460
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0086 | 7 | NA18942.hp2 NA18946.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+584C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023460 | ||||||
chr6:47023686
|
T | A | 1 | a0001c0003t0022g0309 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.451+358A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023686 | ||||||
chr6:47023703
|
C | T | 177 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0115others(174): Show | 206 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.451+341G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023703 | ||||||
chr6:47023780
|
A | G | 1 | a0001c0001t0004g0247 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.451+264T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023780 | ||||||
chr6:47023782
|
C | A | 1 | a0001c0001t0031g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.451+262G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023782 | ||||||
chr6:47023978
|
G | A | 1 | a0002c0002t0006g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.451+66C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023978 | ||||||
chr6:47024035
|
G | C | 2 | a0001c0001t0007g0024a0001c0001t0027g0145 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.451+9C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47024035 | ||||||
chr6:47024223
|
C | G | 1 | a0001c0003t0004g0314 | 1 | HG03195.hp1 | splice_region_variant&intron_variant | LOW | c.278-6G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024223 | ||||||
chr6:47024288
|
AT | A | 9 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.278-72delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024288 | ||||||
chr6:47024322
|
T | C | 66 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(63): Show | 81 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.278-105A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024322 | ||||||
chr6:47024429
|
G | A | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.278-212C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024429 | ||||||
chr6:47024458
|
G | A | 3 | a0001c0003t0001g0218a0003c0004t0007g0158a0003c0004t0007g0159 | 3 | HG01069.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.278-241C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024458 | ||||||
chr6:47024467
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0050 | 6 | NA18942.hp2 NA18946.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-250T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024467 | ||||||
chr6:47024594
|
G | A | 8 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0008t0006g0330others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-377C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024594 | ||||||
chr6:47024603
|
C | T | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.278-386G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024603 | ||||||
chr6:47024806
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.278-589C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024806 | ||||||
chr6:47024843
|
G | A | 3 | a0002c0008t0003g0030a0002c0008t0003g0216a0002c0008t0003g0217 | 4 | HG02280.hp1 HG02630.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-626C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024843 | ||||||
chr6:47024850
|
A | G | 54 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(51): Show | 68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.278-633T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024850 | ||||||
chr6:47024873
|
A | G | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.278-656T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024873 | ||||||
chr6:47024942
|
T | C | 1 | a0003c0004t0007g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.278-725A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024942 | ||||||
chr6:47024958
|
G | A | 3 | a0001c0001t0004g0292a0001c0001t0004g0293a0001c0001t0044g0291 | 3 | HG00642.hp1 HG01192.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.278-741C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024958 | ||||||
chr6:47025171
|
A | G | 54 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(51): Show | 68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.277+683T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025171 | ||||||
chr6:47025245
|
C | A | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.277+609G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025245 | ||||||
chr6:47025304
|
A | C | 8 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0008t0006g0330others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+550T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025304 | ||||||
chr6:47025539
|
T | G | 2 | a0002c0024t0043g0325a0013c0023t0001g0111 | 2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.277+315A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025539 | ||||||
chr6:47025553
|
C | T | 4 | a0001c0001t0018g0134a0001c0001t0018g0215a0006c0010t0019g0125others(1): Show | 4 | HG01255.hp1 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+301G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025553 | ||||||
chr6:47025554
|
G | A | 1 | a0012c0020t0003g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.277+300C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025554 | ||||||
chr6:47025570
|
G | A | 8 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.277+284C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025570 | ||||||
chr6:47025746
|
A | T | 6 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133others(3): Show | 7 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+108T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025746 | ||||||
chr6:47025809
|
C | T | 8 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0008t0006g0330others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+45G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025809 | ||||||
chr6:47025826
|
T | C | 2 | a0002c0024t0043g0325a0013c0023t0001g0111 | 2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.277+28A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025826 | ||||||
chr6:47026011
|
GAGAA | G | 54 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(51): Show | 68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.128-12_128-9delTTC others(1): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026011 | ||||||
chr6:47026102
|
A | G | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128-99T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026102 | ||||||
chr6:47026207
|
C | T | 4 | a0002c0008t0006g0330a0005c0009t0006g0331a0005c0009t0021g0328others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-204G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026207 | ||||||
chr6:47026240
|
C | T | 1 | a0001c0003t0037g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.128-237G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026240 | ||||||
chr6:47026472
|
T | C | 1 | a0001c0003t0004g0311 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.128-469A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026472 | ||||||
chr6:47026581
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.128-578G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026581 | ||||||
chr6:47026585
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.128-582A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026585 | ||||||
chr6:47026709
|
G | A | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.128-706C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026709 | ||||||
chr6:47026725
|
G | A | 2 | a0002c0024t0043g0325a0002c0025t0032g0041 | 2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.128-722C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026725 | ||||||
chr6:47026769
|
C | T | 1 | a0001c0003t0017g0198 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.128-766G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026769 | ||||||
chr6:47026801
|
C | T | 8 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-798G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026801 | ||||||
chr6:47026826
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.128-823A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026826 | ||||||
chr6:47026907
|
A | C | 1 | a0002c0002t0006g0301 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127+797T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026907 | ||||||
chr6:47026938
|
A | T | 8 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+766T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026938 | ||||||
chr6:47027028
|
A | T | 54 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(51): Show | 68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.127+676T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027028 | ||||||
chr6:47027066
|
G | A | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.127+638C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027066 | ||||||
chr6:47027074
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.127+630A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027074 | ||||||
chr6:47027083
|
G | A | 2 | a0002c0002t0008g0154a0002c0019t0008g0153 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.127+621C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027083 | ||||||
chr6:47027172
|
A | T | 1 | a0002c0002t0008g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127+532T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027172 | ||||||
chr6:47027195
|
G | T | 6 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133others(3): Show | 7 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+509C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027195 | ||||||
chr6:47027222
|
C | G | 3 | a0002c0024t0043g0325a0002c0025t0032g0041a0013c0023t0001g0111 | 3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.127+482G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027222 | ||||||
chr6:47027310
|
C | T | 2 | a0002c0024t0043g0325a0002c0025t0032g0041 | 2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.127+394G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027310 | ||||||
chr6:47027311
|
G | A | 44 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(41): Show | 56 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.127+393C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027311 | ||||||
chr6:47027406
|
C | T | 1 | a0010c0022t0006g0307 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.127+298G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027406 | ||||||
chr6:47027507
|
G | A | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.127+197C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027507 | ||||||
chr6:47027695
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.127+9C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027695 | ||||||
chr6:47027765
|
T | C | 6 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0204others(3): Show | 6 | HG01070.hp1 HG01261.hp1 HG02683.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.70-4A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027765 | ||||||
chr6:47027772
|
G | GA | 97 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0001g0156others(94): Show | 110 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.70-12dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027772 | ||||||
chr6:47027836
|
A | C | 2 | a0001c0001t0007g0024a0001c0001t0027g0145 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.70-75T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027836 | ||||||
chr6:47027888
|
G | A | 5 | a0004c0005t0002g0034a0004c0005t0002g0255a0004c0005t0002g0262others(2): Show | 6 | NA18941.hp1 NA18995.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-127C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027888 | ||||||
chr6:47027935
|
A | G | 3 | a0002c0024t0043g0325a0002c0025t0032g0041a0013c0023t0001g0111 | 3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.70-174T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027935 | ||||||
chr6:47028066
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.70-305C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028066 | ||||||
chr6:47028069
|
A | T | 1 | a0001c0001t0002g0263 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.70-308T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028069 | ||||||
chr6:47028097
|
C | T | 8 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-336G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028097 | ||||||
chr6:47028161
|
A | G | 2 | a0001c0001t0012g0120a0001c0001t0012g0182 | 2 | NA18965.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.70-400T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028161 | ||||||
chr6:47028182
|
T | C | 3 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044 | 3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.70-421A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028182 | ||||||
chr6:47028265
|
T | C | 36 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(33): Show | 47 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.70-504A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028265 | ||||||
chr6:47028280
|
C | T | 8 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-519G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028280 | ||||||
chr6:47028332
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.70-571A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028332 | ||||||
chr6:47028481
|
C | T | 1 | a0002c0019t0008g0153 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+512G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028481 | ||||||
chr6:47028482
|
C | G | 198 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0109others(195): Show | 228 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(225): Show |
intron_variant | MODIFIER | c.69+511G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028482 | ||||||
chr6:47028515
|
C | T | 1 | a0002c0008t0003g0030 | 2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.69+478G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028515 | ||||||
chr6:47028540
|
G | A | 1 | a0001c0001t0001g0027 | 2 | NA18964.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.69+453C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028540 | ||||||
chr6:47028553
|
T | C | 2 | a0001c0001t0004g0286a0001c0001t0004g0287 | 2 | NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.69+440A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028553 | ||||||
chr6:47028671
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.69+322G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028671 | ||||||
chr6:47028702
|
C | A | 2 | a0002c0024t0043g0325a0002c0025t0032g0041 | 2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.69+291G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028702 | ||||||
chr6:47028742
|
C | A | 10 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044others(7): Show | 12 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+251G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028742 | ||||||
chr6:47028880
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.69+113T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028880 | ||||||
chr6:47028958
|
G | T | 3 | a0002c0024t0043g0325a0002c0025t0032g0041a0013c0023t0001g0111 | 3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.69+35C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028958 | ||||||
chr6:47029298
|
A | G | 2 | a0002c0002t0020g0326a0002c0002t0020g0327 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-43-194T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029298 | ||||||
chr6:47029358
|
G | GT | 12 | a0001c0001t0001g0083a0001c0001t0018g0134a0001c0001t0018g0215others(9): Show | 12 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-255dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029358 | ||||||
chr6:47029370
|
T | A | 3 | a0002c0024t0043g0325a0002c0025t0032g0041a0013c0023t0001g0111 | 3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-266A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029370 | ||||||
chr6:47029374
|
C | T | 98 | a0001c0001t0001g0056a0001c0001t0001g0113a0001c0001t0001g0127others(95): Show | 111 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-43-270G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029374 | ||||||
chr6:47029415
|
G | A | 2 | a0002c0024t0043g0325a0002c0025t0032g0041 | 2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-311C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029415 | ||||||
chr6:47029651
|
C | G | 5 | a0002c0002t0008g0040a0002c0002t0008g0154a0002c0002t0010g0007others(2): Show | 7 | HG01884.hp1 HG02572.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-547G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029651 | ||||||
chr6:47029794
|
T | C | 8 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-690A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029794 | ||||||
chr6:47030050
|
A | G | 2 | a0002c0024t0043g0325a0002c0025t0032g0041 | 2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-946T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030050 | ||||||
chr6:47030063
|
T | C | 8 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0008t0006g0330others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-959A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030063 | ||||||
chr6:47030171
|
C | T | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-1067G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030171 | ||||||
chr6:47030174
|
G | A | 1 | a0001c0001t0012g0182 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-43-1070C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030174 | ||||||
chr6:47030179
|
G | A | 96 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0001g0156others(93): Show | 109 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-43-1075C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030179 | ||||||
chr6:47030341
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-43-1237G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030341 | ||||||
chr6:47030511
|
G | A | 2 | a0002c0008t0006g0330a0005c0009t0021g0329 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-43-1407C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030511 | ||||||
chr6:47030538
|
A | T | 2 | a0002c0024t0043g0325a0002c0025t0032g0041 | 2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-1434T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030538 | ||||||
chr6:47030576
|
A | ATG | 78 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-43-1474_-43-1473d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | ||||||
chr6:47030576
|
A | ATGTG | 34 | a0001c0001t0001g0028a0001c0001t0001g0048a0001c0001t0001g0080others(31): Show | 35 | HG00544.hp2 HG00621.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-43-1476_-43-1473d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | ||||||
chr6:47030576
|
A | ATGTGTG | 36 | a0001c0001t0001g0156a0001c0001t0001g0191a0001c0001t0001g0201others(33): Show | 42 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-43-1478_-43-1473d others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | ||||||
chr6:47030576
|
A | ATGTGTGT others(1): Show |
27 | a0001c0001t0002g0011a0001c0001t0002g0035a0001c0001t0002g0228others(24): Show | 31 | HG00609.hp1 HG01168.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.-43-1480_-43-1473d others(10): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | ||||||
chr6:47030576
|
A | ATGTGTGT others(3): Show |
13 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0002g0005others(10): Show | 17 | HG03239.hp2 HG03486.hp1 HG04115.hp2 others(14): Show |
intron_variant | MODIFIER | c.-43-1482_-43-1473d others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | ||||||
chr6:47030576
|
ATG | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0017others(38): Show | 51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.-43-1474_-43-1473d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | ||||||
chr6:47030576
|
ATGTGTG | A | 6 | a0001c0001t0004g0039a0001c0003t0004g0314a0002c0002t0003g0122others(3): Show | 7 | HG02145.hp2 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-1478_-43-1473d others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | ||||||
chr6:47030576
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0005g0192 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-43-1482_-43-1473d others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | ||||||
chr6:47030618
|
G | A | 1 | a0001c0001t0001g0017 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-43-1514C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030618 | ||||||
chr6:47030619
|
T | C | 1 | a0001c0001t0001g0017 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-43-1515A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030619 | ||||||
chr6:47030732
|
T | C | 6 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133others(3): Show | 7 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-1628A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030732 | ||||||
chr6:47030734
|
G | T | 1 | a0001c0001t0002g0259 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-43-1630C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030734 | ||||||
chr6:47030745
|
A | G | 1 | a0002c0002t0003g0059 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-43-1641T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030745 | ||||||
chr6:47030769
|
C | CT | 36 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(33): Show | 47 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-43-1666dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030769 | ||||||
chr6:47030771
|
C | T | 80 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(77): Show | 96 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.-43-1667G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030771 | ||||||
chr6:47030864
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0095 | 2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.-43-1760C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030864 | ||||||
chr6:47030947
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-43-1843C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030947 | ||||||
chr6:47030953
|
G | A | 2 | a0002c0024t0043g0325a0002c0025t0032g0041 | 2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-1849C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030953 | ||||||
chr6:47031255
|
G | A | 6 | a0002c0002t0011g0131a0002c0002t0011g0132a0002c0002t0011g0133others(3): Show | 7 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-2151C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031255 | ||||||
chr6:47031257
|
GTCTCTCT others(6): Show |
G | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-2166_-43-2154d others(15): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031257 | ||||||
chr6:47031257
|
GTCTCTCT others(54): Show |
G | 1 | a0001c0001t0002g0230 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-43-2214_-43-2154d others(63): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031257 | ||||||
chr6:47031270
|
T | TTC | 8 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | HG01175.hp2 HG03710.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-2168_-43-2167d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031270 | ||||||
chr6:47031270
|
TTCTC | T | 13 | a0001c0001t0002g0258a0001c0001t0002g0278a0001c0001t0005g0165others(10): Show | 13 | HG01255.hp1 HG01891.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43-2170_-43-2167d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031270 | ||||||
chr6:47031288
|
CTCTCTGT others(56): Show |
C | 1 | a0001c0001t0002g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-43-2247_-43-2185d others(65): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031288 | ||||||
chr6:47031331
|
TTCTCTCT others(25): Show |
T | 3 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044 | 3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-43-2259_-43-2228d others(34): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031331 | ||||||
chr6:47031332
|
T | C | 2 | a0001c0001t0001g0202a0002c0002t0003g0068 | 2 | HG02129.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-43-2228A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031332 | ||||||
chr6:47031333
|
C | T | 2 | a0001c0001t0001g0202a0002c0002t0003g0068 | 2 | HG02129.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-43-2229G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031333 | ||||||
chr6:47031335
|
CTCTCTCT others(9): Show |
C | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-2247_-43-2232d others(18): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031335 | ||||||
chr6:47031347
|
C | G | 1 | a0002c0024t0043g0325 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-43-2243G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031347 | ||||||
chr6:47031349
|
CTG | C | 5 | a0002c0002t0003g0068a0002c0008t0003g0030a0002c0008t0003g0216others(2): Show | 6 | HG01106.hp1 HG02129.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-2247_-43-2246d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031349 | ||||||
chr6:47031351
|
G | C | 4 | a0001c0001t0001g0202a0002c0002t0011g0131a0002c0002t0011g0132others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-2247C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
G | GTC | 32 | a0001c0001t0001g0017a0001c0001t0001g0058a0001c0001t0001g0097others(29): Show | 33 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-43-2249_-43-2248d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
G | GTCTC | 12 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0100others(9): Show | 13 | HG00438.hp1 HG00642.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-43-2251_-43-2248d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
G | GTCTCTC | 3 | a0001c0001t0001g0028a0001c0001t0001g0136a0001c0001t0004g0280 | 4 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-2253_-43-2248d others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
G | GTCTCTCT others(3): Show |
2 | a0001c0012t0005g0140a0001c0012t0005g0141 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-43-2257_-43-2248d others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
G | GTCTCTCT others(5): Show |
1 | a0001c0003t0004g0311 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-43-2259_-43-2248d others(14): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
G | GTCTCTCT others(7): Show |
1 | a0001c0003t0023g0038 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-43-2261_-43-2248d others(16): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
GTC | G | 80 | a0001c0001t0001g0026a0001c0001t0001g0056a0001c0001t0001g0127others(77): Show | 94 | HG00099.hp1 HG00544.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-43-2249_-43-2248d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
GTCTC | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0166others(37): Show | 57 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.-43-2251_-43-2248d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
GTCTCTC | G | 10 | a0001c0001t0005g0124a0001c0001t0007g0024a0001c0001t0018g0134others(7): Show | 11 | HG01255.hp1 HG01884.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-2253_-43-2248d others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
GTCTCTCT others(1): Show |
G | 8 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 9 | HG00639.hp1 HG02135.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-2255_-43-2248d others(10): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
GTCTCTCT others(3): Show |
G | 2 | a0001c0001t0004g0039a0002c0002t0003g0102 | 3 | HG01928.hp1 HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-43-2257_-43-2248d others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031351
|
GTCTCTCT others(5): Show |
G | 1 | a0005c0009t0006g0331 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-2259_-43-2248d others(14): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | ||||||
chr6:47031353
|
C | G | 6 | a0001c0001t0001g0175a0001c0001t0001g0202a0001c0001t0002g0225others(3): Show | 6 | HG01167.hp2 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-2249G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031353 | ||||||
chr6:47031355
|
C | G | 4 | a0002c0002t0003g0068a0002c0008t0003g0030a0002c0008t0003g0216others(1): Show | 5 | HG02129.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-2251G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031355 | ||||||
chr6:47031363
|
C | G | 1 | a0013c0023t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-2259G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031363 | ||||||
chr6:47031386
|
T | C | 2 | a0002c0024t0043g0325a0002c0025t0032g0041 | 2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-2282A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031386 | ||||||
chr6:47031416
|
C | T | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-43-2312G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031416 | ||||||
chr6:47031459
|
A | G | 84 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0001g0156others(81): Show | 96 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-43-2355T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031459 | ||||||
chr6:47031508
|
T | G | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-43-2404A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031508 | ||||||
chr6:47031524
|
C | T | 1 | a0004c0005t0002g0255 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-43-2420G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031524 | ||||||
chr6:47031572
|
G | C | 3 | a0002c0024t0043g0325a0002c0025t0032g0041a0013c0023t0001g0111 | 3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-2468C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031572 | ||||||
chr6:47031695
|
G | C | 1 | a0002c0002t0003g0102 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-43-2591C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031695 | ||||||
chr6:47031744
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 5 | HG03491.hp2 HG03492.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-2640C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031744 | ||||||
chr6:47031809
|
C | T | 64 | a0001c0001t0001g0048a0001c0001t0001g0067a0001c0001t0001g0115others(61): Show | 78 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.-43-2705G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031809 | ||||||
chr6:47031935
|
T | C | 2 | a0001c0001t0004g0254a0002c0002t0003g0164 | 2 | HG02132.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.-43-2831A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031935 | ||||||
chr6:47031968
|
C | G | 1 | a0003c0004t0007g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-43-2864G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031968 | ||||||
chr6:47032088
|
G | A | 8 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0006g0320others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-2984C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032088 | ||||||
chr6:47032139
|
G | T | 1 | a0002c0002t0011g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-43-3035C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032139 | ||||||
chr6:47032158
|
C | T | 1 | a0010c0022t0006g0307 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-43-3054G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032158 | ||||||
chr6:47032159
|
G | A | 2 | a0001c0012t0005g0140a0001c0012t0005g0141 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-43-3055C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032159 | ||||||
chr6:47032270
|
G | A | 4 | a0002c0002t0009g0037a0002c0002t0009g0297a0002c0002t0009g0298others(1): Show | 5 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-3166C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032270 | ||||||
chr6:47032274
|
C | A | 80 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0001g0156others(77): Show | 92 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-43-3170G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032274 | ||||||
chr6:47032325
|
G | A | 8 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0008t0006g0330others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-3221C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032325 | ||||||
chr6:47032389
|
A | T | 2 | a0002c0024t0043g0325a0002c0025t0032g0041 | 2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-3285T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032389 | ||||||
chr6:47032389
|
AT | A | 3 | a0002c0008t0003g0030a0002c0008t0003g0216a0002c0008t0003g0217 | 4 | HG02280.hp1 HG02630.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-3286delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032389 | ||||||
chr6:47032479
|
T | C | 5 | a0001c0001t0001g0058a0001c0001t0004g0224a0001c0001t0004g0247others(2): Show | 5 | HG00438.hp2 HG02155.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-3375A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032479 | ||||||
chr6:47032769
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-43-3665T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032769 | ||||||
chr6:47032785
|
T | C | 151 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0067others(148): Show | 176 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.-43-3681A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032785 | ||||||
chr6:47032793
|
G | C | 4 | a0001c0001t0018g0134a0002c0002t0011g0131a0002c0002t0011g0132others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-3689C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032793 | ||||||
chr6:47032925
|
C | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(99): Show | 131 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.-43-3821G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032925 | ||||||
chr6:47032929
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-43-3825T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032929 | ||||||
chr6:47032954
|
G | C | 7 | a0001c0001t0018g0134a0001c0001t0018g0215a0002c0002t0011g0131others(4): Show | 7 | HG00741.hp2 HG01243.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-3850C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032954 | ||||||
chr6:47032987
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-43-3883G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032987 | ||||||
chr6:47032988
|
G | A | 2 | a0001c0003t0004g0314a0001c0003t0023g0038 | 3 | HG02630.hp2 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-43-3884C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032988 | ||||||
chr6:47033056
|
T | C | 1 | a0001c0001t0002g0241 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-43-3952A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033056 | ||||||
chr6:47033066
|
C | T | 1 | a0005c0009t0006g0331 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-3962G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033066 | ||||||
chr6:47033165
|
T | A | 6 | a0002c0002t0006g0320a0002c0002t0006g0321a0002c0002t0006g0322others(3): Show | 6 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-4061A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033165 | ||||||
chr6:47033175
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-43-4071C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033175 | ||||||
chr6:47033229
|
C | T | 6 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 7 | HG02148.hp2 NA18939.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-4125G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033229 | ||||||
chr6:47033292
|
A | G | 7 | a0001c0001t0007g0024a0001c0001t0018g0215a0001c0001t0027g0145others(4): Show | 8 | HG02257.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-4188T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033292 | ||||||
chr6:47033306
|
G | A | 1 | a0001c0001t0001g0020 | 2 | NA18951.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-43-4202C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033306 | ||||||
chr6:47033382
|
C | T | 3 | a0001c0006t0001g0021a0001c0006t0001g0110a0013c0023t0001g0111 | 4 | HG02145.hp1 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-4278G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033382 | ||||||
chr6:47033416
|
C | T | 5 | a0002c0002t0006g0320a0002c0002t0006g0321a0002c0002t0006g0322others(2): Show | 5 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-4312G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033416 | ||||||
chr6:47033463
|
T | C | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-43-4359A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033463 | ||||||
chr6:47033499
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-43-4395G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033499 | ||||||
chr6:47033602
|
G | A | 1 | a0002c0002t0013g0144 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-43-4498C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033602 | ||||||
chr6:47033711
|
C | T | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-4607G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033711 | ||||||
chr6:47033721
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-43-4617G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033721 | ||||||
chr6:47033773
|
G | C | 13 | a0001c0001t0039g0332a0002c0002t0006g0320a0002c0002t0006g0321others(10): Show | 13 | HG01106.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43-4669C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033773 | ||||||
chr6:47033775
|
G | C | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-4671C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033775 | ||||||
chr6:47033846
|
C | A | 5 | a0001c0001t0018g0134a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-4742G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033846 | ||||||
chr6:47033876
|
T | C | 86 | a0001c0001t0002g0011a0001c0001t0002g0031a0001c0001t0002g0035others(83): Show | 93 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-43-4772A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033876 | ||||||
chr6:47033903
|
T | A | 86 | a0001c0001t0002g0011a0001c0001t0002g0031a0001c0001t0002g0035others(83): Show | 93 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-43-4799A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033903 | ||||||
chr6:47034227
|
T | C | 1 | a0014c0018t0006g0281 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-43-5123A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034227 | ||||||
chr6:47034281
|
T | C | 3 | a0003c0004t0007g0219a0003c0004t0007g0220a0003c0004t0007g0221 | 3 | HG01255.hp2 HG03704.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-43-5177A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034281 | ||||||
chr6:47034326
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | NA18965.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-43-5222C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034326 | ||||||
chr6:47034364
|
T | C | 3 | a0002c0002t0003g0004a0002c0002t0003g0106a0002c0002t0003g0107 | 7 | NA18960.hp1 NA18997.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-5260A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034364 | ||||||
chr6:47034407
|
C | T | 1 | a0002c0002t0003g0047 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-43-5303G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034407 | ||||||
chr6:47034425
|
T | C | 1 | a0002c0002t0009g0304 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-5321A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034425 | ||||||
chr6:47034594
|
A | G | 5 | a0001c0003t0001g0142a0001c0003t0001g0143a0001c0012t0005g0140others(2): Show | 5 | HG02257.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-5490T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034594 | ||||||
chr6:47034734
|
G | C | 1 | a0005c0009t0006g0331 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-5630C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034734 | ||||||
chr6:47034963
|
C | A | 1 | a0001c0001t0039g0332 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-5859G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034963 | ||||||
chr6:47035116
|
C | T | 1 | a0001c0017t0026g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-43-6012G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035116 | ||||||
chr6:47035125
|
A | G | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-6021T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035125 | ||||||
chr6:47035173
|
G | C | 8 | a0001c0001t0018g0215a0001c0003t0001g0218a0002c0008t0003g0030others(5): Show | 9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-6069C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035173 | ||||||
chr6:47035187
|
G | A | 1 | a0001c0001t0001g0023 | 2 | HG01516.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-43-6083C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035187 | ||||||
chr6:47035269
|
A | C | 1 | a0001c0001t0004g0296 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-43-6165T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035269 | ||||||
chr6:47035407
|
T | TA | 4 | a0001c0001t0018g0134a0002c0002t0011g0131a0002c0002t0011g0132others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-6304dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035407 | ||||||
chr6:47035454
|
TA | T | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-6351delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035454 | ||||||
chr6:47035510
|
T | A | 1 | a0011c0021t0002g0282 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-43-6406A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035510 | ||||||
chr6:47035604
|
C | T | 8 | a0001c0001t0002g0294a0001c0001t0004g0290a0001c0001t0004g0292others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-6500G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035604 | ||||||
chr6:47035704
|
A | G | 2 | a0001c0001t0002g0242a0001c0001t0002g0283 | 2 | NA18967.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-44+6487T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035704 | ||||||
chr6:47035732
|
C | T | 1 | a0001c0001t0007g0024 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-44+6459G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035732 | ||||||
chr6:47035740
|
G | A | 113 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 128 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-44+6451C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035740 | ||||||
chr6:47035920
|
G | C | 1 | a0002c0002t0006g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-44+6271C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035920 | ||||||
chr6:47035921
|
G | T | 1 | a0002c0002t0006g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-44+6270C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035921 | ||||||
chr6:47035956
|
C | A | 8 | a0001c0001t0002g0294a0001c0001t0004g0290a0001c0001t0004g0292others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+6235G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035956 | ||||||
chr6:47036046
|
C | A | 1 | a0002c0002t0011g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+6145G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036046 | ||||||
chr6:47036060
|
A | G | 1 | a0001c0001t0035g0289 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-44+6131T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036060 | ||||||
chr6:47036162
|
G | A | 1 | a0002c0002t0011g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+6029C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036162 | ||||||
chr6:47036266
|
A | T | 25 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0036others(22): Show | 33 | HG01074.hp1 HG01255.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-44+5925T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036266 | ||||||
chr6:47036269
|
A | C | 1 | a0001c0001t0001g0136 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-44+5922T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036269 | ||||||
chr6:47036290
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0004g0305 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-44+5901A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036290 | ||||||
chr6:47036355
|
A | G | 10 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0235others(7): Show | 10 | HG00735.hp2 HG01346.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44+5836T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036355 | ||||||
chr6:47036380
|
C | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0012g0025 | 4 | HG02148.hp2 NA18969.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+5811G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036380 | ||||||
chr6:47036459
|
G | A | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-44+5732C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036459 | ||||||
chr6:47036515
|
C | A | 1 | a0001c0017t0026g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-44+5676G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036515 | ||||||
chr6:47036547
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0162others(3): Show | 11 | HG02132.hp1 NA18939.hp1 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+5644T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036547 | ||||||
chr6:47036549
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(76): Show | 112 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.-44+5642T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036549 | ||||||
chr6:47036742
|
A | G | 3 | a0002c0002t0013g0160a0003c0004t0007g0158a0003c0004t0007g0159 | 3 | HG00741.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-44+5449T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036742 | ||||||
chr6:47037156
|
T | C | 1 | a0001c0001t0002g0283 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-44+5035A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037156 | ||||||
chr6:47037169
|
T | C | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+5022A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037169 | ||||||
chr6:47037215
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-44+4976C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037215 | ||||||
chr6:47037247
|
G | A | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+4944C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037247 | ||||||
chr6:47037398
|
G | C | 1 | a0001c0001t0036g0284 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-44+4793C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037398 | ||||||
chr6:47037405
|
A | T | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+4786T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037405 | ||||||
chr6:47037414
|
A | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(250): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.-44+4777T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037414 | ||||||
chr6:47037490
|
A | G | 8 | a0001c0001t0002g0031a0001c0001t0002g0225a0001c0001t0002g0228others(5): Show | 9 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+4701T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037490 | ||||||
chr6:47037616
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0004g0039 | 3 | HG02717.hp2 HG02886.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-44+4575G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037616 | ||||||
chr6:47037762
|
C | A | 8 | a0001c0001t0018g0215a0001c0003t0001g0218a0002c0008t0003g0030others(5): Show | 9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+4429G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037762 | ||||||
chr6:47038009
|
C | T | 1 | a0001c0001t0002g0288 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-44+4182G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038009 | ||||||
chr6:47038063
|
G | C | 8 | a0001c0001t0018g0215a0001c0003t0001g0218a0002c0008t0003g0030others(5): Show | 9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+4128C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038063 | ||||||
chr6:47038101
|
T | C | 1 | a0001c0001t0002g0285 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-44+4090A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038101 | ||||||
chr6:47038216
|
A | G | 113 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0012others(110): Show | 128 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-44+3975T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038216 | ||||||
chr6:47038289
|
C | A | 25 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0036others(22): Show | 33 | HG01074.hp1 HG01255.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-44+3902G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038289 | ||||||
chr6:47038289
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-44+3902G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038289 | ||||||
chr6:47038542
|
G | C | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01175.hp2 HG03927.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+3649C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038542 | ||||||
chr6:47038604
|
C | T | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+3587G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038604 | ||||||
chr6:47038627
|
T | A | 8 | a0001c0001t0002g0294a0001c0001t0004g0290a0001c0001t0004g0292others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+3564A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038627 | ||||||
chr6:47038645
|
A | G | 25 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0036others(22): Show | 33 | HG01074.hp1 HG01255.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-44+3546T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038645 | ||||||
chr6:47038677
|
A | G | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+3514T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038677 | ||||||
chr6:47038740
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-44+3451G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038740 | ||||||
chr6:47038817
|
C | T | 3 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044 | 3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-44+3374G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038817 | ||||||
chr6:47038818
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-44+3373C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038818 | ||||||
chr6:47038906
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(258): Show | 315 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.-44+3285T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038906 | ||||||
chr6:47038920
|
G | A | 2 | a0001c0001t0004g0286a0001c0001t0004g0287 | 2 | NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-44+3271C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038920 | ||||||
chr6:47039081
|
TC | T | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+3109delG | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039081 | ||||||
chr6:47039171
|
A | G | 3 | a0001c0001t0005g0155a0002c0002t0008g0154a0002c0019t0008g0153 | 3 | HG02965.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-44+3020T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039171 | ||||||
chr6:47039189
|
G | T | 19 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(16): Show | 20 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+3002C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039189 | ||||||
chr6:47039217
|
G | T | 12 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0299others(9): Show | 17 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-44+2974C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039217 | ||||||
chr6:47039290
|
T | C | 1 | a0001c0001t0002g0288 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-44+2901A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039290 | ||||||
chr6:47039411
|
T | A | 8 | a0001c0001t0018g0215a0001c0003t0001g0218a0002c0008t0003g0030others(5): Show | 9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+2780A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039411 | ||||||
chr6:47039504
|
G | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-44+2687C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039504 | ||||||
chr6:47039527
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(150): Show | 192 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.-44+2664A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039527 | ||||||
chr6:47039646
|
C | T | 1 | a0001c0003t0022g0295 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-44+2545G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039646 | ||||||
chr6:47039651
|
T | C | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+2540A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039651 | ||||||
chr6:47039753
|
G | A | 1 | a0002c0002t0011g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+2438C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039753 | ||||||
chr6:47039872
|
G | A | 8 | a0001c0001t0002g0294a0001c0001t0004g0290a0001c0001t0004g0292others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+2319C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039872 | ||||||
chr6:47039886
|
T | G | 4 | a0001c0001t0018g0134a0002c0002t0011g0131a0002c0002t0011g0132others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+2305A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039886 | ||||||
chr6:47039965
|
A | AAAAT | 5 | a0001c0001t0018g0134a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+2222_-44+2225d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039965 | ||||||
chr6:47039984
|
A | G | 1 | a0007c0011t0005g0152 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-44+2207T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039984 | ||||||
chr6:47040012
|
G | T | 109 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 124 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-44+2179C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040012 | ||||||
chr6:47040015
|
T | C | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+2176A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040015 | ||||||
chr6:47040066
|
G | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(100): Show | 139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-44+2125C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040066 | ||||||
chr6:47040103
|
A | G | 1 | a0001c0001t0004g0224 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-44+2088T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040103 | ||||||
chr6:47040116
|
C | A | 109 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0012others(106): Show | 124 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-44+2075G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040116 | ||||||
chr6:47040190
|
C | T | 5 | a0001c0001t0018g0134a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+2001G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040190 | ||||||
chr6:47040336
|
G | A | 1 | a0001c0001t0004g0039 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-44+1855C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040336 | ||||||
chr6:47040365
|
G | A | 8 | a0001c0001t0018g0215a0001c0003t0001g0218a0002c0008t0003g0030others(5): Show | 9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+1826C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040365 | ||||||
chr6:47040380
|
G | A | 26 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0036others(23): Show | 34 | HG01074.hp1 HG01255.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.-44+1811C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040380 | ||||||
chr6:47040385
|
T | A | 8 | a0001c0001t0039g0332a0002c0002t0020g0326a0002c0002t0020g0327others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+1806A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040385 | ||||||
chr6:47040488
|
TA | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(135): Show | 175 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.-44+1702delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040488 | ||||||
chr6:47040493
|
A | T | 111 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0012others(108): Show | 126 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.-44+1698T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040493 | ||||||
chr6:47040573
|
G | T | 4 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044others(1): Show | 4 | HG02055.hp1 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+1618C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040573 | ||||||
chr6:47040621
|
C | T | 1 | a0001c0001t0016g0223 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-44+1570G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040621 | ||||||
chr6:47040683
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-44+1508A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040683 | ||||||
chr6:47040912
|
T | G | 2 | a0001c0001t0004g0317a0001c0001t0004g0318 | 2 | HG01515.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-44+1279A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040912 | ||||||
chr6:47041033
|
G | A | 3 | a0001c0001t0018g0134a0002c0002t0011g0132a0002c0002t0011g0133 | 3 | HG01243.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+1158C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041033 | ||||||
chr6:47041056
|
T | C | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01175.hp2 HG03927.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+1135A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041056 | ||||||
chr6:47041152
|
C | T | 5 | a0002c0002t0006g0320a0002c0002t0006g0321a0002c0002t0006g0322others(2): Show | 5 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+1039G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041152 | ||||||
chr6:47041175
|
T | C | 1 | a0001c0001t0004g0319 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-44+1016A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041175 | ||||||
chr6:47041257
|
A | G | 5 | a0001c0001t0018g0134a0002c0002t0011g0131a0002c0002t0011g0132others(2): Show | 5 | HG01243.hp1 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+934T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041257 | ||||||
chr6:47041456
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(104): Show | 143 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-44+735G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041456 | ||||||
chr6:47041861
|
C | T | 3 | a0002c0002t0003g0042a0002c0002t0003g0043a0002c0002t0003g0044 | 3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-44+330G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041861 | ||||||
chr6:47042042
|
C | A | 1 | a0009c0015t0001g0222 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-44+149G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47042042 | ||||||
chr6:47042075
|
T | G | 14 | a0001c0001t0004g0039a0001c0001t0039g0332a0002c0002t0006g0320others(11): Show | 15 | HG01106.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-44+116A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47042075 | ||||||
chr6:47042090
|
A | T | 1 | a0002c0025t0032g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-44+101T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47042090 | ||||||
chr6:47042112
|
A | G | 1 | a0002c0002t0008g0040 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-44+79T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47042112 |