geneid | 2483 |
---|---|
ensemblid | ENSG00000109536.13 |
hgncid | 3954 |
symbol | FRG1 |
name | FSHD region gene 1 |
refseq_nuc | NM_004477.3 |
refseq_prot | NP_004468.1 |
ensembl_nuc | ENST00000226798.9 |
ensembl_prot | ENSP00000226798.4 |
mane_status | MANE Select |
chr | chr4 |
start | 189940872 |
end | 189963192 |
strand | + |
ver | v1.2 |
region | chr4:189940872-189963192 |
region5000 | chr4:189935872-189968192 |
regionname0 | FRG1_chr4_189940872_189963192 |
regionname5000 | FRG1_chr4_189935872_189968192 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 258 | 346 | 93 | 56 | 140 | 14 | 42 | 112 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0002 | 0/0 | 258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 777 | 155 | 21 | 34 | 65 | 8 | 26 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
c0002 | 0/0 | 777 | 114 | 29 | 16 | 50 | 6 | 13 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
c0003 | 0/0 | 777 | 77 | 43 | 6 | 25 | 0 | 3 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
c0004 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 202 | 154 | 21 | 34 | 65 | 8 | 25 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0002 | 0/0 | 202 | 69 | 21 | 14 | 18 | 5 | 11 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0003 | 0/0 | 202 | 39 | 13 | 1 | 25 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0004 | 0/0 | 202 | 36 | 2 | 2 | 30 | 1 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0005 | 0/0 | 202 | 31 | 24 | 4 | 0 | 0 | 3 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0006 | 0/0 | 202 | 5 | 5 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0007 | 0/0 | 202 | 5 | 4 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0008 | 0/0 | 202 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0009 | 0/0 | 202 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0010 | 0/0 | 202 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0011 | 0/0 | 202 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0012 | 0/0 | 202 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
t0013 | 0/0 | 202 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 66 | 1 | 12 | 40 | 3 | 10 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0002 | 0/0 | 47 | 6 | 11 | 17 | 5 | 8 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0003 | 0/0 | 30 | 8 | 0 | 22 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0004 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0005 | 0/0 | 6 | 1 | 2 | 2 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0006 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0007 | 0/1 | 6 | 1 | 2 | 0 | 1 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0008 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0013 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0019 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 777 | 155 | 21 | 34 | 65 | 8 | 26 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0002 | 0/0 | 777 | 114 | 29 | 16 | 50 | 6 | 13 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0003 | 0/0 | 777 | 77 | 43 | 6 | 25 | 0 | 3 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0002c0004 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 978 | 154 | 21 | 34 | 65 | 8 | 25 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0001t0012 | 0/0 | 978 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0002t0002 | 0/0 | 978 | 68 | 20 | 14 | 18 | 5 | 11 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0002t0004 | 0/0 | 978 | 36 | 2 | 2 | 30 | 1 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0002t0006 | 0/0 | 978 | 5 | 5 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0002t0008 | 0/0 | 978 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0002t0010 | 0/0 | 978 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0002t0011 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0002t0013 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0003t0002 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0003t0003 | 0/0 | 978 | 39 | 13 | 1 | 25 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0003t0005 | 0/0 | 978 | 30 | 23 | 4 | 0 | 0 | 3 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0003t0007 | 0/0 | 978 | 5 | 4 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0001c0003t0009 | 0/0 | 978 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
a0002c0004t0005 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | copy fasta | chr4 | 189935872 | 189968192 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 65 | 1 | 12 | 40 | 3 | 9 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0004 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0005 | 0/0 | 6 | 1 | 2 | 2 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0007 | 0/1 | 6 | 1 | 2 | 0 | 1 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0002 | 0/0 | 31 | 5 | 10 | 5 | 4 | 7 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0002 | 0/0 | 16 | 1 | 1 | 12 | 1 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0006g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0008g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0010g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0011g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0002t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0003 | 0/0 | 30 | 8 | 0 | 22 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0008 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0019 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0007g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0007g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0001c0003t0009g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
a0002c0004t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | FIN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00408 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00438 | hp1 | a0001 | c0002 | t0004 | g0114 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00558 | hp2 | a0001 | c0002 | t0004 | g0121 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00597 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00621 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00642 | hp2 | a0001 | c0002 | t0004 | g0036 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0119 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00735 | hp2 | a0001 | c0003 | t0007 | g0066 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00741 | hp1 | a0001 | c0003 | t0005 | g0008 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01081 | hp2 | a0001 | c0003 | t0005 | g0010 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01099 | hp1 | a0001 | c0003 | t0005 | g0008 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01109 | hp1 | a0001 | c0003 | t0005 | g0008 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0108 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01496 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01884 | hp1 | a0001 | c0003 | t0005 | g0086 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01891 | hp1 | a0001 | c0003 | t0005 | g0011 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01891 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01934 | hp2 | a0001 | c0003 | t0003 | g0064 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02055 | hp1 | a0001 | c0003 | t0005 | g0008 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0120 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02083 | hp2 | a0001 | c0002 | t0004 | g0111 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02129 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02132 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | CDX | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02257 | hp1 | a0001 | c0003 | t0005 | g0008 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02258 | hp1 | a0001 | c0002 | t0006 | g0021 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02258 | hp2 | a0001 | c0003 | t0002 | g0098 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02280 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02523 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02572 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02572 | hp2 | a0001 | c0003 | t0005 | g0093 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0101 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02615 | hp2 | a0001 | c0003 | t0003 | g0052 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02622 | hp1 | a0001 | c0003 | t0003 | g0061 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02647 | hp2 | a0001 | c0003 | t0009 | g0022 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02723 | hp1 | a0001 | c0003 | t0007 | g0016 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02723 | hp2 | a0001 | c0003 | t0005 | g0010 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02809 | hp2 | a0001 | c0003 | t0005 | g0033 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02818 | hp1 | a0001 | c0003 | t0007 | g0016 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0100 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02886 | hp1 | a0001 | c0003 | t0005 | g0011 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0099 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02922 | hp1 | a0001 | c0003 | t0005 | g0011 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02922 | hp2 | a0001 | c0003 | t0007 | g0016 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0041 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02976 | hp1 | a0001 | c0002 | t0011 | g0044 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02976 | hp2 | a0001 | c0003 | t0005 | g0035 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0047 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03098 | hp2 | a0001 | c0003 | t0005 | g0008 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03130 | hp1 | a0001 | c0003 | t0005 | g0010 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03139 | hp1 | a0002 | c0004 | t0005 | g0094 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03139 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03195 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03195 | hp2 | a0001 | c0002 | t0006 | g0045 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03209 | hp1 | a0001 | c0002 | t0006 | g0021 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03225 | hp1 | a0001 | c0002 | t0013 | g0048 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03453 | hp1 | a0001 | c0003 | t0005 | g0033 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03453 | hp2 | a0001 | c0003 | t0005 | g0034 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03486 | hp1 | a0001 | c0003 | t0005 | g0087 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03486 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03516 | hp1 | a0001 | c0003 | t0005 | g0034 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03540 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03579 | hp2 | a0001 | c0003 | t0005 | g0055 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03654 | hp2 | a0001 | c0002 | t0010 | g0096 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03688 | hp2 | a0001 | c0003 | t0005 | g0019 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03831 | hp1 | a0001 | c0001 | t0012 | g0001 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03834 | hp1 | a0001 | c0003 | t0005 | g0019 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03942 | hp2 | a0001 | c0003 | t0005 | g0092 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0039 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04204 | hp2 | a0001 | c0002 | t0004 | g0002 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18522 | hp1 | a0001 | c0003 | t0005 | g0010 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18522 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18906 | hp1 | a0001 | c0003 | t0003 | g0053 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18941 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18942 | hp1 | a0001 | c0002 | t0004 | g0122 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18945 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18947 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18948 | hp2 | a0001 | c0002 | t0004 | g0049 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18952 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18954 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18956 | hp1 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18957 | hp1 | a0001 | c0002 | t0008 | g0040 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18959 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18962 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18965 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18967 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18968 | hp1 | a0001 | c0002 | t0004 | g0112 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18970 | hp2 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18972 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18974 | hp1 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18975 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18979 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18980 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18981 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18981 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18994 | hp1 | a0001 | c0003 | t0003 | g0063 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18995 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18999 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19000 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19000 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19002 | hp2 | a0001 | c0002 | t0004 | g0097 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19003 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19004 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19006 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19009 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19012 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19030 | hp2 | a0001 | c0003 | t0005 | g0010 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19043 | hp2 | a0001 | c0002 | t0006 | g0046 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19054 | hp2 | a0001 | c0003 | t0003 | g0065 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19065 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19065 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19068 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19068 | hp2 | a0001 | c0002 | t0008 | g0040 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19075 | hp1 | a0001 | c0002 | t0004 | g0107 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19075 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19079 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19081 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19082 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19083 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19090 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19090 | hp2 | a0001 | c0003 | t0003 | g0062 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19240 | hp1 | a0001 | c0003 | t0007 | g0091 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0041 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA20129 | hp1 | a0001 | c0003 | t0009 | g0022 | AFR | ASW | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA20129 | hp2 | a0001 | c0003 | t0003 | g0051 | AFR | ASW | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA20805 | hp1 | a0001 | c0002 | t0004 | g0002 | EUR | TSI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0105 | EUR | TSI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | GIH | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02486 | hp2 | a0001 | c0003 | t0003 | g0058 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG02559 | hp2 | a0001 | c0003 | t0005 | g0035 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03471 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG03471 | hp2 | a0001 | c0003 | t0005 | g0011 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
HG06807 | hp2 | a0001 | c0003 | t0005 | g0011 | AFR | USA | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA21309 | hp1 | a0001 | c0003 | t0005 | g0019 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:189961868
|
G | A | 1 | a0002 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.676G>A | p.Glu226Lys | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/9 | 814/978 | 676/777 | 226/258 | chr4 | 189961868 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:189941027
|
C | T | 3 | a0001c0002a0001c0003a0002c0004 | 192 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(189): Show |
synonymous_variant | LOW | c.18C>T | p.Tyr6Tyr | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 156/978 | 18/777 | 6/258 | chr4 | 189941027 | ||
chr4:189955040
|
C | T | 1 | a0001c0002 | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
synonymous_variant | LOW | c.321C>T | p.Ile107Ile | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/9 | 459/978 | 321/777 | 107/258 | chr4 | 189955040 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:189940880
|
C | G | 5 | a0001c0003t0003a0001c0003t0005a0001c0003t0007others(2): Show | 77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-130C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 130 | chr4 | 189940880 | |||||
chr4:189940887
|
G | A | 2 | a0001c0003t0005a0002c0004t0005 | 31 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-123G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 123 | chr4 | 189940887 | |||||
chr4:189940892
|
C | T | 1 | a0001c0002t0013 | 1 | HG03225.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-118C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | chr4 | 189940892 | ||||||
chr4:189940923
|
C | T | 1 | a0001c0002t0008 | 2 | NA18957.hp1 NA19068.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | chr4 | 189940923 | ||||||
chr4:189940928
|
T | C | 13 | a0001c0002t0002a0001c0002t0004a0001c0002t0006others(10): Show | 192 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(189): Show |
5_prime_UTR_variant | MODIFIER | c.-82T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 82 | chr4 | 189940928 | |||||
chr4:189940929
|
C | G | 5 | a0001c0003t0003a0001c0003t0005a0001c0003t0007others(2): Show | 77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-81C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | chr4 | 189940929 | ||||||
chr4:189940948
|
C | T | 6 | a0001c0002t0004a0001c0002t0011a0001c0003t0003others(3): Show | 109 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-62C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 62 | chr4 | 189940948 | |||||
chr4:189940949
|
C | G | 1 | a0001c0002t0010 | 1 | HG03654.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 61 | chr4 | 189940949 | |||||
chr4:189940949
|
C | T | 1 | a0001c0002t0013 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 61 | chr4 | 189940949 | |||||
chr4:189940971
|
A | G | 5 | a0001c0003t0003a0001c0003t0005a0001c0003t0007others(2): Show | 77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-39A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 39 | chr4 | 189940971 | |||||
chr4:189940983
|
C | T | 1 | a0001c0003t0009 | 2 | HG02647.hp2 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-27C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 27 | chr4 | 189940983 | |||||
chr4:189940987
|
C | T | 5 | a0001c0003t0003a0001c0003t0005a0001c0003t0007others(2): Show | 77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-23C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 23 | chr4 | 189940987 | |||||
chr4:189940996
|
A | C | 1 | a0001c0002t0006 | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-14A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 14 | chr4 | 189940996 | |||||
chr4:189940999
|
T | C | 5 | a0001c0003t0003a0001c0003t0005a0001c0003t0007others(2): Show | 77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-11T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 11 | chr4 | 189940999 | |||||
chr4:189941000
|
T | G | 5 | a0001c0002t0002a0001c0002t0004a0001c0002t0008others(2): Show | 108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | chr4 | 189941000 | ||||||
chr4:189941009
|
C | T | 1 | a0001c0001t0012 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 1 | chr4 | 189941009 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:189941132
|
C | T | 42 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(39): Show | 106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.62+61C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941132 | ||||||
chr4:189941222
|
C | T | 1 | a0001c0002t0010g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.62+151C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941222 | ||||||
chr4:189941271
|
A | G | 1 | a0001c0002t0004g0020 | 3 | NA18956.hp1 NA18970.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.62+200A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941271 | ||||||
chr4:189941291
|
G | A | 1 | a0001c0002t0004g0097 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.62+220G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941291 | ||||||
chr4:189941356
|
G | A | 48 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(45): Show | 113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.62+285G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941356 | ||||||
chr4:189941402
|
C | T | 1 | a0001c0003t0009g0022 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.62+331C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941402 | ||||||
chr4:189941434
|
C | T | 5 | a0001c0002t0002g0015a0001c0002t0002g0117a0001c0002t0002g0118others(2): Show | 8 | HG00733.hp2 HG01168.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.62+363C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941434 | ||||||
chr4:189941554
|
C | G | 1 | a0001c0001t0001g0095 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.62+483C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941554 | ||||||
chr4:189941637
|
T | C | 2 | a0001c0002t0002g0036a0001c0002t0004g0036 | 2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.62+566T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941637 | ||||||
chr4:189941643
|
C | T | 1 | a0001c0002t0002g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.62+572C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941643 | ||||||
chr4:189941726
|
A | G | 3 | a0001c0003t0005g0008a0001c0003t0005g0093a0002c0004t0005g0094 | 8 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.62+655A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941726 | ||||||
chr4:189941813
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.62+742G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941813 | ||||||
chr4:189941872
|
T | C | 1 | a0001c0001t0001g0012 | 4 | HG00280.hp1 HG00639.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.62+801T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941872 | ||||||
chr4:189941972
|
C | G | 44 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(41): Show | 108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.62+901C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941972 | ||||||
chr4:189942067
|
T | A | 3 | a0001c0003t0003g0051a0001c0003t0003g0052a0001c0003t0003g0053 | 3 | HG02615.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.62+996T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942067 | ||||||
chr4:189942442
|
T | G | 1 | a0001c0002t0002g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.63-760T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942442 | ||||||
chr4:189942443
|
C | T | 1 | a0001c0002t0002g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.63-759C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942443 | ||||||
chr4:189942505
|
A | G | 1 | a0001c0003t0005g0035 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.63-697A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942505 | ||||||
chr4:189942563
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.63-639T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942563 | ||||||
chr4:189942567
|
A | G | 1 | a0001c0003t0005g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.63-635A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942567 | ||||||
chr4:189942587
|
T | A | 50 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(47): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.63-615T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942587 | ||||||
chr4:189942688
|
G | A | 1 | a0001c0003t0005g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63-514G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942688 | ||||||
chr4:189942860
|
C | A | 44 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(41): Show | 108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.63-342C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942860 | ||||||
chr4:189942930
|
C | G | 1 | a0001c0002t0002g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.63-272C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942930 | ||||||
chr4:189942978
|
A | G | 1 | a0001c0003t0009g0022 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63-224A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942978 | ||||||
chr4:189942997
|
C | T | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.63-205C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942997 | ||||||
chr4:189943355
|
T | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0056 | 3 | NA18950.hp1 NA18967.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.133+83T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943355 | ||||||
chr4:189943388
|
A | G | 1 | a0001c0003t0007g0091 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133+116A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943388 | ||||||
chr4:189943487
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0057 | 3 | NA18972.hp1 NA18980.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.133+215G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943487 | ||||||
chr4:189943499
|
A | G | 1 | a0001c0002t0002g0042 | 2 | HG02155.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.133+227A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943499 | ||||||
chr4:189943777
|
G | A | 1 | a0001c0003t0002g0098 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.133+505G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943777 | ||||||
chr4:189943798
|
A | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+526A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943798 | ||||||
chr4:189943882
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.133+610A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943882 | ||||||
chr4:189943998
|
G | C | 1 | a0001c0002t0010g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133+726G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943998 | ||||||
chr4:189944133
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+861C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944133 | ||||||
chr4:189944240
|
G | A | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+968G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944240 | ||||||
chr4:189944241
|
A | G | 1 | a0001c0002t0010g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133+969A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944241 | ||||||
chr4:189944246
|
G | A | 1 | a0001c0002t0010g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133+974G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944246 | ||||||
chr4:189944613
|
CT | C | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+1352delT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189944613 | |||||
chr4:189944721
|
G | A | 1 | a0001c0001t0001g0025 | 2 | NA18950.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.133+1449G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944721 | ||||||
chr4:189944773
|
G | C | 43 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(40): Show | 107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.133+1501G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944773 | ||||||
chr4:189944895
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+1623T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944895 | ||||||
chr4:189944941
|
A | C | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+1669A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944941 | ||||||
chr4:189945043
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.133+1771C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945043 | ||||||
chr4:189945243
|
T | A | 3 | a0001c0003t0003g0051a0001c0003t0003g0052a0001c0003t0003g0053 | 3 | HG02615.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.133+1971T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945243 | ||||||
chr4:189945257
|
T | C | 1 | a0001c0003t0005g0035 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.133+1985T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945257 | ||||||
chr4:189945376
|
C | T | 1 | a0001c0002t0002g0115 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.133+2104C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945376 | ||||||
chr4:189945386
|
A | G | 13 | a0001c0003t0005g0008a0001c0003t0005g0010a0001c0003t0005g0011others(10): Show | 31 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.133+2114A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945386 | ||||||
chr4:189945400
|
C | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+2128C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945400 | ||||||
chr4:189945463
|
T | C | 1 | a0001c0003t0003g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133+2191T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945463 | ||||||
chr4:189945526
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.133+2254C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945526 | ||||||
chr4:189945608
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.133+2336C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945608 | ||||||
chr4:189945609
|
G | C | 1 | a0001c0001t0001g0059 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.133+2337G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945609 | ||||||
chr4:189945698
|
A | G | 1 | a0001c0001t0001g0007 | 6 | HG00140.hp2 HG01070.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+2426A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945698 | ||||||
chr4:189945773
|
A | C | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+2501A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945773 | ||||||
chr4:189945852
|
T | C | 2 | a0001c0003t0005g0010a0001c0003t0005g0086 | 6 | HG01081.hp2 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+2580T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945852 | ||||||
chr4:189946175
|
C | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+2903C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946175 | ||||||
chr4:189946280
|
CATAAA | C | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+3012_133+3016d others(7): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189946280 | |||||
chr4:189946286
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.133+3014A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946286 | ||||||
chr4:189946311
|
C | CAA | 9 | a0001c0002t0002g0110a0001c0002t0004g0049a0001c0002t0004g0111others(6): Show | 10 | HG02083.hp2 HG02258.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+3053_133+3054d others(4): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189946311 | |||||
chr4:189946311
|
C | CAAA | 36 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(33): Show | 100 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.133+3052_133+3054d others(5): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189946311 | |||||
chr4:189946336
|
T | C | 1 | a0001c0002t0006g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.133+3064T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946336 | ||||||
chr4:189946395
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.133+3123G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946395 | ||||||
chr4:189946634
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.133+3362C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946634 | ||||||
chr4:189946672
|
G | A | 1 | a0001c0001t0001g0026 | 2 | NA19060.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.133+3400G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946672 | ||||||
chr4:189946709
|
T | C | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+3437T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946709 | ||||||
chr4:189946714
|
A | G | 1 | a0001c0002t0010g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133+3442A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946714 | ||||||
chr4:189946783
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.133+3511T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946783 | ||||||
chr4:189946845
|
G | T | 46 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(43): Show | 110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.133+3573G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946845 | ||||||
chr4:189947099
|
T | G | 72 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(69): Show | 185 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.133+3827T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947099 | ||||||
chr4:189947143
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.133+3871G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947143 | ||||||
chr4:189947146
|
C | A | 1 | a0001c0003t0003g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133+3874C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947146 | ||||||
chr4:189947241
|
A | G | 1 | a0001c0001t0001g0012 | 4 | HG00280.hp1 HG00639.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+3969A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947241 | ||||||
chr4:189947246
|
T | G | 77 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(74): Show | 192 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.133+3974T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947246 | ||||||
chr4:189947252
|
T | C | 13 | a0001c0003t0005g0008a0001c0003t0005g0010a0001c0003t0005g0011others(10): Show | 31 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.133+3980T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947252 | ||||||
chr4:189947286
|
T | C | 1 | a0001c0003t0009g0022 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.133+4014T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947286 | ||||||
chr4:189947321
|
C | T | 76 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(73): Show | 191 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.133+4049C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947321 | ||||||
chr4:189947322
|
G | C | 76 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(73): Show | 191 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.133+4050G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947322 | ||||||
chr4:189947324
|
C | CATAAG | 76 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(73): Show | 191 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.133+4054_133+4055i others(7): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189947324 | |||||
chr4:189947442
|
C | A | 7 | a0001c0003t0003g0003a0001c0003t0003g0058a0001c0003t0003g0061others(4): Show | 36 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.133+4170C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947442 | ||||||
chr4:189947478
|
G | A | 3 | a0001c0003t0005g0008a0001c0003t0005g0093a0002c0004t0005g0094 | 8 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+4206G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947478 | ||||||
chr4:189947703
|
C | G | 9 | a0001c0003t0003g0003a0001c0003t0003g0051a0001c0003t0003g0053others(6): Show | 38 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(35): Show |
intron_variant | MODIFIER | c.133+4431C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947703 | ||||||
chr4:189947718
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(11): Show | 32 | HG00280.hp1 HG00639.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.134-4444A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947718 | ||||||
chr4:189947764
|
T | C | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-4398T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947764 | ||||||
chr4:189947915
|
C | G | 73 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(70): Show | 186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.134-4247C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947915 | ||||||
chr4:189948092
|
G | A | 1 | a0001c0002t0002g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.134-4070G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948092 | ||||||
chr4:189948118
|
G | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-4044G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948118 | ||||||
chr4:189948206
|
T | G | 10 | a0001c0003t0003g0003a0001c0003t0003g0051a0001c0003t0003g0052others(7): Show | 39 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(36): Show |
intron_variant | MODIFIER | c.134-3956T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948206 | ||||||
chr4:189948222
|
G | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-3940G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948222 | ||||||
chr4:189948244
|
G | A | 43 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(40): Show | 107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.134-3918G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948244 | ||||||
chr4:189948256
|
G | C | 43 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(40): Show | 107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.134-3906G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948256 | ||||||
chr4:189948511
|
C | G | 7 | a0001c0003t0003g0003a0001c0003t0003g0058a0001c0003t0003g0061others(4): Show | 36 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.134-3651C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948511 | ||||||
chr4:189948520
|
A | G | 1 | a0002c0004t0005g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.134-3642A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948520 | ||||||
chr4:189948549
|
T | A | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-3613T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948549 | ||||||
chr4:189948828
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.134-3334C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948828 | ||||||
chr4:189948841
|
C | A | 42 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(39): Show | 106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.134-3321C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948841 | ||||||
chr4:189948968
|
A | C | 7 | a0001c0003t0003g0003a0001c0003t0003g0058a0001c0003t0003g0061others(4): Show | 36 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.134-3194A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948968 | ||||||
chr4:189948969
|
G | A | 1 | a0001c0003t0003g0061 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.134-3193G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948969 | ||||||
chr4:189949318
|
T | G | 1 | a0001c0002t0004g0121 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-2844T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949318 | ||||||
chr4:189949356
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.134-2806A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949356 | ||||||
chr4:189949417
|
A | G | 5 | a0001c0003t0005g0010a0001c0003t0005g0034a0001c0003t0005g0035others(2): Show | 11 | HG01081.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-2745A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949417 | ||||||
chr4:189949765
|
T | C | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-2397T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949765 | ||||||
chr4:189949769
|
A | G | 1 | a0001c0003t0005g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.134-2393A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949769 | ||||||
chr4:189949817
|
T | C | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-2345T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949817 | ||||||
chr4:189949920
|
G | A | 1 | a0001c0002t0002g0117 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.134-2242G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949920 | ||||||
chr4:189949924
|
A | G | 1 | a0001c0002t0002g0109 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.134-2238A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949924 | ||||||
chr4:189949988
|
C | T | 1 | a0001c0002t0002g0108 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.134-2174C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949988 | ||||||
chr4:189950042
|
T | TTTTG | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-2104_134-2101d others(6): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189950042 | |||||
chr4:189950421
|
T | C | 1 | a0001c0002t0011g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.134-1741T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950421 | ||||||
chr4:189950660
|
A | C | 1 | a0001c0003t0005g0087 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.134-1502A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950660 | ||||||
chr4:189950707
|
A | G | 1 | a0001c0002t0006g0047 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.134-1455A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950707 | ||||||
chr4:189950792
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.134-1370T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950792 | ||||||
chr4:189950841
|
G | A | 73 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(70): Show | 186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.134-1321G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950841 | ||||||
chr4:189950852
|
T | C | 1 | a0001c0003t0009g0022 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.134-1310T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950852 | ||||||
chr4:189950938
|
A | G | 1 | a0001c0002t0010g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.134-1224A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950938 | ||||||
chr4:189950947
|
T | C | 1 | a0001c0002t0006g0021 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.134-1215T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950947 | ||||||
chr4:189951092
|
G | T | 77 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(74): Show | 192 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.134-1070G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951092 | ||||||
chr4:189951304
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.134-858G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951304 | ||||||
chr4:189951388
|
A | G | 1 | a0001c0002t0002g0041 | 2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.134-774A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951388 | ||||||
chr4:189951444
|
C | T | 1 | a0001c0002t0010g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.134-718C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951444 | ||||||
chr4:189951489
|
CA | C | 32 | a0001c0001t0001g0057a0001c0002t0006g0021a0001c0002t0006g0045others(29): Show | 83 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(80): Show |
intron_variant | MODIFIER | c.134-656delA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189951489 | |||||
chr4:189951489
|
CAA | C | 45 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(42): Show | 109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.134-657_134-656del others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189951489 | |||||
chr4:189951539
|
C | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-623C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951539 | ||||||
chr4:189951552
|
C | T | 2 | a0001c0003t0005g0019a0001c0003t0005g0092 | 4 | HG03688.hp2 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-610C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951552 | ||||||
chr4:189951623
|
T | C | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-539T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951623 | ||||||
chr4:189951633
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.134-529G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951633 | ||||||
chr4:189951650
|
C | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-512C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951650 | ||||||
chr4:189951727
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.134-435A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951727 | ||||||
chr4:189951739
|
C | T | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-423C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951739 | ||||||
chr4:189951881
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.134-281C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951881 | ||||||
chr4:189951888
|
A | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-274A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951888 | ||||||
chr4:189951939
|
T | C | 13 | a0001c0003t0005g0008a0001c0003t0005g0010a0001c0003t0005g0011others(10): Show | 31 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.134-223T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951939 | ||||||
chr4:189951962
|
T | G | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-200T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951962 | ||||||
chr4:189952005
|
T | G | 73 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(70): Show | 186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.134-157T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189952005 | ||||||
chr4:189952007
|
A | C | 73 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(70): Show | 186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.134-155A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189952007 | ||||||
chr4:189952029
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.134-133A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189952029 | ||||||
chr4:189952099
|
CA | C | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-55delA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189952099 | |||||
chr4:189952367
|
C | G | 1 | a0001c0003t0009g0022 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259+80C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189952367 | ||||||
chr4:189952634
|
G | A | 1 | a0001c0001t0001g0025 | 2 | NA18950.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.259+347G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189952634 | ||||||
chr4:189952797
|
G | A | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.260-271G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189952797 | ||||||
chr4:189952860
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.260-208C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189952860 | ||||||
chr4:189953039
|
T | C | 1 | a0001c0003t0009g0022 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.260-29T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189953039 | ||||||
chr4:189953165
|
T | G | 2 | a0001c0003t0005g0010a0001c0003t0005g0086 | 6 | HG01081.hp2 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.317+40T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953165 | ||||||
chr4:189953218
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG00544.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.317+93G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953218 | ||||||
chr4:189953314
|
G | GA | 85 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(82): Show | 212 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.317+197dupA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189953314 | |||||
chr4:189953314
|
G | GAA | 5 | a0001c0003t0005g0010a0001c0003t0005g0034a0001c0003t0005g0035others(2): Show | 11 | HG01081.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+196_317+197dup others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189953314 | |||||
chr4:189953349
|
T | A | 1 | a0001c0001t0001g0067 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.317+224T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953349 | ||||||
chr4:189953357
|
C | T | 1 | a0001c0001t0001g0031 | 2 | NA18747.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.317+232C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953357 | ||||||
chr4:189953359
|
G | A | 1 | a0001c0003t0009g0022 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.317+234G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953359 | ||||||
chr4:189953380
|
G | A | 72 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(69): Show | 184 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.317+255G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953380 | ||||||
chr4:189953600
|
C | T | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.317+475C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953600 | ||||||
chr4:189953622
|
T | C | 4 | a0001c0003t0005g0008a0001c0003t0005g0011a0001c0003t0005g0093others(1): Show | 13 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.317+497T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953622 | ||||||
chr4:189953680
|
T | C | 23 | a0001c0003t0003g0003a0001c0003t0003g0051a0001c0003t0003g0052others(20): Show | 70 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.317+555T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953680 | ||||||
chr4:189953739
|
G | T | 1 | a0001c0003t0009g0022 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.317+614G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953739 | ||||||
chr4:189953746
|
T | TA | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+625dupA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189953746 | |||||
chr4:189953797
|
T | G | 1 | a0001c0003t0005g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.317+672T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953797 | ||||||
chr4:189953883
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0075a0001c0001t0001g0084 | 5 | HG00735.hp1 HG01258.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+758A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953883 | ||||||
chr4:189953901
|
G | A | 3 | a0001c0002t0004g0014a0001c0002t0004g0097a0001c0002t0004g0112 | 6 | NA18947.hp2 NA18965.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.317+776G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953901 | ||||||
chr4:189954036
|
A | G | 1 | a0001c0002t0013g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.317+911A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954036 | ||||||
chr4:189954047
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.317+922A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954047 | ||||||
chr4:189954099
|
A | T | 1 | a0001c0002t0011g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.318-938A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954099 | ||||||
chr4:189954207
|
TA | T | 3 | a0001c0003t0005g0008a0001c0003t0005g0093a0002c0004t0005g0094 | 8 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.318-821delA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189954207 | |||||
chr4:189954382
|
A | G | 1 | a0001c0003t0007g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.318-655A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954382 | ||||||
chr4:189954398
|
TAAG | T | 4 | a0001c0003t0005g0019a0001c0003t0005g0033a0001c0003t0005g0087others(1): Show | 7 | HG02809.hp2 HG03453.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.318-637_318-635del others(3): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189954398 | |||||
chr4:189954399
|
AAG | A | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.318-634_318-633del others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189954399 | |||||
chr4:189954522
|
A | C | 1 | a0001c0003t0005g0034 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.318-515A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954522 | ||||||
chr4:189954525
|
G | A | 1 | a0001c0002t0010g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.318-512G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954525 | ||||||
chr4:189954593
|
TTC | T | 10 | a0001c0002t0002g0038a0001c0002t0002g0039a0001c0002t0002g0099others(7): Show | 12 | HG00558.hp1 HG02258.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-442_318-441del others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189954593 | |||||
chr4:189954594
|
TC | T | 36 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(33): Show | 99 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.318-442delC | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954594 | ||||||
chr4:189954595
|
C | T | 1 | a0001c0002t0002g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318-442C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954595 | ||||||
chr4:189954621
|
G | T | 1 | a0001c0003t0002g0098 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.318-416G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954621 | ||||||
chr4:189954654
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.318-383G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954654 | ||||||
chr4:189954788
|
G | T | 1 | a0001c0002t0004g0107 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.318-249G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954788 | ||||||
chr4:189955455
|
A | ATCT | 73 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(70): Show | 186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.432+306_432+308dup others(3): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 189955455 | |||||
chr4:189955682
|
G | GT | 4 | a0001c0003t0005g0019a0001c0003t0005g0033a0001c0003t0005g0087others(1): Show | 7 | HG02809.hp2 HG03453.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+532dupT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 189955682 | |||||
chr4:189955831
|
A | T | 1 | a0001c0002t0002g0106 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.432+680A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189955831 | ||||||
chr4:189955917
|
A | G | 2 | a0001c0002t0010g0096a0001c0002t0011g0044 | 2 | HG02976.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.432+766A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189955917 | ||||||
chr4:189956037
|
A | G | 2 | a0001c0003t0003g0052a0001c0003t0003g0053 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.432+886A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956037 | ||||||
chr4:189956138
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.432+987A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956138 | ||||||
chr4:189956201
|
A | T | 59 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(56): Show | 153 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.432+1050A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956201 | ||||||
chr4:189956408
|
T | G | 1 | a0001c0002t0002g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.433-990T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956408 | ||||||
chr4:189956413
|
G | C | 1 | a0001c0002t0006g0021 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.433-985G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956413 | ||||||
chr4:189956554
|
C | T | 1 | a0001c0002t0006g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.433-844C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956554 | ||||||
chr4:189956555
|
A | G | 74 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(71): Show | 187 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.433-843A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956555 | ||||||
chr4:189956672
|
G | T | 1 | a0001c0002t0002g0105 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.433-726G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956672 | ||||||
chr4:189956709
|
T | G | 56 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(53): Show | 133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.433-689T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956709 | ||||||
chr4:189956724
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.433-674G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956724 | ||||||
chr4:189956834
|
G | C | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-564G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956834 | ||||||
chr4:189957037
|
G | A | 10 | a0001c0003t0003g0003a0001c0003t0003g0051a0001c0003t0003g0052others(7): Show | 39 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(36): Show |
intron_variant | MODIFIER | c.433-361G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957037 | ||||||
chr4:189957167
|
CCTA | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0082 | 9 | HG02083.hp1 HG02698.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-227_433-225del others(3): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 189957167 | |||||
chr4:189957225
|
T | A | 1 | a0001c0003t0003g0062 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.433-173T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957225 | ||||||
chr4:189957230
|
G | T | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-168G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957230 | ||||||
chr4:189957258
|
G | C | 1 | a0001c0002t0004g0122 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.433-140G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957258 | ||||||
chr4:189957317
|
A | G | 56 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(53): Show | 133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.433-81A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957317 | ||||||
chr4:189957357
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0073 | 13 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.433-41A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957357 | ||||||
chr4:189957362
|
T | C | 1 | a0001c0003t0007g0091 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.433-36T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957362 | ||||||
chr4:189957383
|
A | AT | 74 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(71): Show | 187 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.433-12dupT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 189957383 | |||||
chr4:189957552
|
C | CTGTA | 11 | a0001c0003t0003g0003a0001c0003t0003g0051a0001c0003t0003g0052others(8): Show | 41 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(38): Show |
intron_variant | MODIFIER | c.537+52_537+55dupGT others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189957552 | |||||
chr4:189957587
|
G | C | 43 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(40): Show | 107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.537+85G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189957587 | ||||||
chr4:189957653
|
A | G | 57 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(54): Show | 134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.537+151A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189957653 | ||||||
chr4:189957672
|
T | G | 57 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(54): Show | 134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.537+170T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189957672 | ||||||
chr4:189957752
|
C | T | 5 | a0001c0003t0005g0010a0001c0003t0005g0034a0001c0003t0005g0035others(2): Show | 11 | HG01081.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.537+250C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189957752 | ||||||
chr4:189958105
|
G | GTTTTCTC | 43 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(40): Show | 107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.537+608_537+614dup others(7): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189958105 | |||||
chr4:189958138
|
C | A | 4 | a0001c0003t0005g0008a0001c0003t0005g0011a0001c0003t0005g0093others(1): Show | 13 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.537+636C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958138 | ||||||
chr4:189958170
|
C | T | 68 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(65): Show | 175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.537+668C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958170 | ||||||
chr4:189958233
|
T | C | 1 | a0001c0003t0003g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.537+731T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958233 | ||||||
chr4:189958292
|
C | T | 5 | a0001c0003t0005g0010a0001c0003t0005g0034a0001c0003t0005g0035others(2): Show | 11 | HG01081.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.537+790C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958292 | ||||||
chr4:189958345
|
T | C | 68 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(65): Show | 175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.537+843T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958345 | ||||||
chr4:189958596
|
G | A | 1 | a0001c0002t0013g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.537+1094G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958596 | ||||||
chr4:189958633
|
G | A | 2 | a0001c0003t0003g0052a0001c0003t0003g0053 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.537+1131G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958633 | ||||||
chr4:189958666
|
T | C | 5 | a0001c0002t0002g0009a0001c0002t0002g0038a0001c0002t0002g0102others(2): Show | 11 | HG00558.hp1 HG03710.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.537+1164T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958666 | ||||||
chr4:189958672
|
A | C | 1 | a0001c0001t0001g0018 | 3 | HG00735.hp1 HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.537+1170A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958672 | ||||||
chr4:189958696
|
A | T | 1 | a0001c0001t0001g0056 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.537+1194A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958696 | ||||||
chr4:189958774
|
A | C | 57 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(54): Show | 134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.537+1272A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958774 | ||||||
chr4:189958781
|
A | AT | 49 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(46): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.537+1285dupT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189958781 | |||||
chr4:189958827
|
A | G | 1 | a0001c0001t0001g0017 | 3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.537+1325A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958827 | ||||||
chr4:189959022
|
G | C | 1 | a0001c0001t0001g0028 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.537+1520G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959022 | ||||||
chr4:189959121
|
A | G | 2 | a0001c0002t0002g0037a0001c0002t0002g0099 | 3 | HG02895.hp1 HG02897.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.537+1619A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959121 | ||||||
chr4:189959136
|
A | G | 68 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(65): Show | 175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.538-1612A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959136 | ||||||
chr4:189959194
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.538-1554T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959194 | ||||||
chr4:189959254
|
A | G | 57 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(54): Show | 134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.538-1494A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959254 | ||||||
chr4:189959475
|
G | A | 1 | a0001c0003t0009g0022 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.538-1273G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959475 | ||||||
chr4:189959508
|
C | T | 4 | a0001c0003t0005g0008a0001c0003t0005g0011a0001c0003t0005g0093others(1): Show | 13 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.538-1240C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959508 | ||||||
chr4:189959649
|
A | G | 1 | a0001c0002t0011g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.538-1099A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959649 | ||||||
chr4:189959698
|
G | A | 57 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(54): Show | 134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.538-1050G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959698 | ||||||
chr4:189959894
|
TACCAGAA others(60): Show |
T | 1 | a0001c0003t0005g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.538-810_538-744del others(67): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189959894 | |||||
chr4:189959940
|
C | T | 1 | a0001c0002t0008g0040 | 2 | NA18957.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.538-808C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959940 | ||||||
chr4:189960114
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0080 | 3 | HG02109.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.538-634G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960114 | ||||||
chr4:189960283
|
T | C | 56 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(53): Show | 133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.538-465T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960283 | ||||||
chr4:189960381
|
C | T | 57 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(54): Show | 134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.538-367C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960381 | ||||||
chr4:189960536
|
A | G | 42 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(39): Show | 106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.538-212A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960536 | ||||||
chr4:189960552
|
A | T | 11 | a0001c0003t0003g0003a0001c0003t0003g0051a0001c0003t0003g0052others(8): Show | 41 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(38): Show |
intron_variant | MODIFIER | c.538-196A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960552 | ||||||
chr4:189960658
|
AATC | A | 10 | a0001c0003t0003g0003a0001c0003t0003g0051a0001c0003t0003g0052others(7): Show | 39 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(36): Show |
intron_variant | MODIFIER | c.538-86_538-84delAT others(1): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189960658 | |||||
chr4:189960678
|
T | C | 1 | a0001c0001t0001g0029 | 2 | HG00099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.538-70T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960678 | ||||||
chr4:189960699
|
G | C | 1 | a0001c0002t0002g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.538-49G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960699 | ||||||
chr4:189961059
|
G | A | 1 | a0001c0002t0002g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.629+220G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961059 | ||||||
chr4:189961083
|
G | A | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.629+244G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961083 | ||||||
chr4:189961217
|
A | C | 1 | a0001c0003t0005g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.629+378A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961217 | ||||||
chr4:189961338
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.630-484C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961338 | ||||||
chr4:189961418
|
T | C | 1 | a0001c0002t0011g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.630-404T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961418 | ||||||
chr4:189961445
|
T | A | 1 | a0001c0003t0003g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.630-377T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961445 | ||||||
chr4:189961493
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.630-329C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961493 | ||||||
chr4:189961531
|
C | G | 1 | a0001c0002t0011g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.630-291C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961531 | ||||||
chr4:189961537
|
A | G | 1 | a0001c0002t0002g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.630-285A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961537 | ||||||
chr4:189961676
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.630-146G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961676 | ||||||
chr4:189961807
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.630-15A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961807 | ||||||
chr4:189962132
|
C | T | 2 | a0001c0003t0003g0065a0001c0003t0005g0035 | 3 | HG02559.hp2 HG02976.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.740+200C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962132 | ||||||
chr4:189962150
|
T | A | 1 | a0001c0002t0006g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.740+218T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962150 | ||||||
chr4:189962522
|
G | A | 1 | a0001c0002t0002g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.741-571G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962522 | ||||||
chr4:189962559
|
C | CT | 11 | a0001c0003t0003g0003a0001c0003t0003g0051a0001c0003t0003g0052others(8): Show | 41 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(38): Show |
intron_variant | MODIFIER | c.741-526dupT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 189962559 | |||||
chr4:189962567
|
T | TA | 4 | a0001c0002t0006g0021a0001c0002t0006g0045a0001c0002t0006g0046others(1): Show | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.741-525dupA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 189962567 | |||||
chr4:189962704
|
CAAG | C | 2 | a0001c0003t0007g0016a0001c0003t0007g0066 | 4 | HG00735.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-384_741-382del others(3): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 189962704 | |||||
chr4:189962903
|
A | G | 1 | a0001c0002t0013g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.741-190A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962903 | ||||||
chr4:189962930
|
T | C | 57 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(54): Show | 134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.741-163T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962930 | ||||||
chr4:189963062
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.741-31A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189963062 | ||||||
chr4:189963070
|
T | TTTC | 68 | a0001c0002t0002g0002a0001c0002t0002g0009a0001c0002t0002g0015others(65): Show | 175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.741-21_741-20insCT others(1): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 189963070 |