geneid | 100129583 |
---|---|
ensemblid | ENSG00000189157.14 |
hgncid | 34343 |
symbol | FAM47E |
name | family with sequence similarity 47 member E |
refseq_nuc | NM_001136570.3 |
refseq_prot | NP_001130042.1 |
ensembl_nuc | ENST00000424749.7 |
ensembl_prot | ENSP00000409423.2 |
mane_status | MANE Select |
chr | chr4 |
start | 76251721 |
end | 76283783 |
strand | + |
ver | v1.2 |
region | chr4:76251721-76283783 |
region5000 | chr4:76246721-76288783 |
regionname0 | FAM47E_chr4_76251721_76283783 |
regionname5000 | FAM47E_chr4_76246721_76288783 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 393 | 151 | 22 | 22 | 89 | 3 | 14 | 66 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0002 | 0/0 | 393 | 131 | 19 | 28 | 66 | 4 | 14 | 58 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0003 | 0/0 | 393 | 53 | 31 | 3 | 14 | 4 | 1 | 11 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0004 | 0/1 | 393 | 42 | 13 | 11 | 8 | 1 | 8 | 8 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0005 | 0/0 | 393 | 8 | 7 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0006 | 0/0 | 393 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0007 | 0/0 | 393 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0008 | 0/0 | 393 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0009 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0010 | 0/0 | 393 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1182 | 149 | 22 | 22 | 88 | 3 | 13 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0002 | 0/0 | 1182 | 131 | 19 | 28 | 66 | 4 | 14 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0003 | 0/0 | 1182 | 53 | 31 | 3 | 14 | 4 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0004 | 0/0 | 1182 | 39 | 13 | 9 | 8 | 1 | 8 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0005 | 0/0 | 1182 | 8 | 7 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0006 | 0/1 | 1182 | 3 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0007 | 0/0 | 1182 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0008 | 0/0 | 1182 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0009 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0010 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0011 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0012 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
c0013 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 352 | 387 | 88 | 65 | 182 | 12 | 38 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
t0002 | 0/0 | 352 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
t0003 | 0/0 | 352 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
t0004 | 0/0 | 352 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 19 | 1 | 4 | 13 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0002 | 0/0 | 19 | 0 | 6 | 7 | 1 | 5 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0003 | 0/0 | 14 | 2 | 3 | 8 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0004 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0005 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0007 | 0/0 | 8 | 0 | 7 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0008 | 0/0 | 8 | 1 | 4 | 0 | 1 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0009 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0011 | 0/0 | 6 | 0 | 1 | 1 | 1 | 3 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0019 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0029 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0031 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1182 | 149 | 22 | 22 | 88 | 3 | 13 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0001c0010 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0001c0012 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0002c0002 | 0/0 | 1182 | 131 | 19 | 28 | 66 | 4 | 14 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0003c0003 | 0/0 | 1182 | 53 | 31 | 3 | 14 | 4 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0004c0004 | 0/0 | 1182 | 39 | 13 | 9 | 8 | 1 | 8 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0004c0006 | 0/1 | 1182 | 3 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0005c0005 | 0/0 | 1182 | 8 | 7 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0006c0007 | 0/0 | 1182 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0007c0008 | 0/0 | 1182 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0008c0013 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0009c0011 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0010c0009 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1533 | 149 | 22 | 22 | 88 | 3 | 13 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0001c0010t0001 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0001c0012t0001 | 0/0 | 1533 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0002c0002t0001 | 0/0 | 1533 | 130 | 19 | 27 | 66 | 4 | 14 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0002c0002t0003 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0003c0003t0001 | 0/0 | 1533 | 50 | 28 | 3 | 14 | 4 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0003c0003t0002 | 0/0 | 1533 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0003c0003t0004 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0004c0004t0001 | 0/0 | 1533 | 38 | 12 | 9 | 8 | 1 | 8 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0004c0004t0002 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0004c0006t0001 | 0/1 | 1533 | 3 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0005c0005t0001 | 0/0 | 1533 | 8 | 7 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0006c0007t0001 | 0/0 | 1533 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0007c0008t0001 | 0/0 | 1533 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0008c0013t0001 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0009c0011t0001 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
a0010c0009t0001 | 0/0 | 1533 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | copy fasta | chr4 | 76246721 | 76288783 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 18 | 0 | 6 | 7 | 1 | 4 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0003 | 0/0 | 13 | 2 | 2 | 8 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0010t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0001c0012t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0001 | 0/0 | 19 | 1 | 4 | 13 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0004 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0007 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0011 | 0/0 | 6 | 0 | 1 | 1 | 1 | 3 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0019 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0002c0002t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0009 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0003c0003t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0008 | 0/0 | 7 | 1 | 3 | 0 | 1 | 2 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0004t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0006t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0006t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0004c0006t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0005c0005t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0005c0005t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0005c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0005c0005t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0005c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0005c0005t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0006c0007t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0006c0007t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0007c0008t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0008c0013t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0009c0011t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
a0010c0009t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0011 | EUR | GBR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0121 | EUR | FIN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00280 | hp2 | a0003 | c0003 | t0001 | g0200 | EUR | FIN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00323 | hp1 | a0004 | c0004 | t0001 | g0008 | EUR | FIN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00639 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00642 | hp2 | a0004 | c0004 | t0001 | g0014 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00673 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00735 | hp2 | a0010 | c0009 | t0001 | g0041 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00738 | hp2 | a0004 | c0006 | t0001 | g0008 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00741 | hp1 | a0004 | c0004 | t0001 | g0014 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01070 | hp1 | a0004 | c0004 | t0001 | g0014 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01071 | hp2 | a0004 | c0004 | t0001 | g0014 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01109 | hp2 | a0004 | c0004 | t0001 | g0008 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0050 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01167 | hp2 | a0004 | c0004 | t0001 | g0107 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01169 | hp2 | a0003 | c0003 | t0001 | g0050 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01257 | hp2 | a0004 | c0004 | t0001 | g0008 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01358 | hp2 | a0004 | c0004 | t0001 | g0123 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01361 | hp2 | a0004 | c0006 | t0001 | g0127 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0049 | EUR | IBS | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01928 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01934 | hp2 | a0008 | c0013 | t0001 | g0003 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01943 | hp2 | a0004 | c0004 | t0001 | g0008 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0058 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02015 | hp1 | a0001 | c0010 | t0001 | g0164 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02258 | hp1 | a0004 | c0004 | t0001 | g0024 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02280 | hp1 | a0003 | c0003 | t0001 | g0071 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02572 | hp1 | a0003 | c0003 | t0001 | g0203 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02572 | hp2 | a0003 | c0003 | t0002 | g0161 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0170 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02615 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02622 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02630 | hp2 | a0003 | c0003 | t0001 | g0072 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02647 | hp1 | a0004 | c0004 | t0001 | g0008 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02647 | hp2 | a0003 | c0003 | t0001 | g0134 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02717 | hp2 | a0004 | c0004 | t0001 | g0109 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02723 | hp1 | a0005 | c0005 | t0001 | g0052 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02735 | hp1 | a0001 | c0012 | t0001 | g0002 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02735 | hp2 | a0004 | c0004 | t0001 | g0096 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02738 | hp2 | a0005 | c0005 | t0001 | g0175 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02818 | hp1 | a0004 | c0004 | t0001 | g0024 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02895 | hp1 | a0005 | c0005 | t0001 | g0038 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02896 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02897 | hp1 | a0003 | c0003 | t0001 | g0048 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02897 | hp2 | a0005 | c0005 | t0001 | g0038 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02965 | hp1 | a0004 | c0004 | t0001 | g0184 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02970 | hp1 | a0005 | c0005 | t0001 | g0176 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0204 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0030 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03195 | hp1 | a0005 | c0005 | t0001 | g0104 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0174 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0112 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03225 | hp2 | a0004 | c0004 | t0001 | g0108 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03453 | hp1 | a0004 | c0004 | t0001 | g0122 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0179 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03486 | hp2 | a0003 | c0003 | t0001 | g0102 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03491 | hp1 | a0004 | c0004 | t0001 | g0135 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03516 | hp1 | a0004 | c0004 | t0002 | g0101 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03540 | hp1 | a0003 | c0003 | t0002 | g0100 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03654 | hp1 | a0004 | c0004 | t0001 | g0136 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0190 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03704 | hp1 | a0004 | c0004 | t0001 | g0126 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03704 | hp2 | a0004 | c0004 | t0001 | g0008 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0094 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0011 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0077 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03942 | hp2 | a0004 | c0004 | t0001 | g0008 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG04184 | hp2 | a0004 | c0004 | t0001 | g0070 | SAS | BEB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0189 | SAS | STU | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18522 | hp1 | a0003 | c0003 | t0001 | g0103 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0040 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18906 | hp1 | a0004 | c0004 | t0001 | g0165 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0040 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18947 | hp1 | a0004 | c0004 | t0001 | g0158 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18948 | hp1 | a0004 | c0004 | t0001 | g0027 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18948 | hp2 | a0003 | c0003 | t0001 | g0133 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18962 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18962 | hp2 | a0009 | c0011 | t0001 | g0087 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18969 | hp1 | a0004 | c0004 | t0001 | g0047 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18970 | hp2 | a0004 | c0004 | t0001 | g0027 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18974 | hp1 | a0003 | c0003 | t0001 | g0132 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18985 | hp2 | a0004 | c0004 | t0001 | g0144 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18988 | hp1 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18993 | hp1 | a0007 | c0008 | t0001 | g0005 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18995 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA18999 | hp2 | a0004 | c0004 | t0001 | g0027 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19001 | hp2 | a0004 | c0004 | t0001 | g0145 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19012 | hp1 | a0006 | c0007 | t0001 | g0073 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0025 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19030 | hp2 | a0004 | c0004 | t0001 | g0111 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19043 | hp1 | a0003 | c0003 | t0001 | g0199 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19064 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19066 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19074 | hp1 | a0006 | c0007 | t0001 | g0089 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19074 | hp2 | a0004 | c0004 | t0001 | g0047 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19075 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19083 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19089 | hp1 | a0007 | c0008 | t0001 | g0005 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19240 | hp1 | a0003 | c0003 | t0001 | g0187 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0039 | AFR | YRI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0025 | AFR | ASW | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20752 | hp2 | a0003 | c0003 | t0001 | g0049 | EUR | TSI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20805 | hp1 | a0003 | c0003 | t0001 | g0172 | EUR | TSI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0120 | EUR | TSI | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20905 | hp1 | a0004 | c0004 | t0001 | g0114 | SAS | GIH | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02109 | hp2 | a0004 | c0004 | t0001 | g0024 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02486 | hp1 | a0004 | c0004 | t0001 | g0110 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02486 | hp2 | a0005 | c0005 | t0001 | g0168 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03471 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | MSL | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | USA | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | USA | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | USA | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | USA | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA21309 | hp1 | a0003 | c0003 | t0004 | g0025 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
NA21309 | hp2 | a0005 | c0005 | t0001 | g0052 | AFR | LWK | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
homoSapiens_chm13v2 | hp1 | a0004 | c0006 | t0001 | g0124 | REF | REF | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0181 | REF | REF | FAM47E_chr4_76246721_76288783 | FAM47E | chr4 | 76246721 | 76288783 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76251793
|
T | C | 1 | a0006 | 2 | NA19012.hp1 NA19074.hp1 |
missense_variant | MODERATE | c.47T>C | p.Val16Ala | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/8 | 73/1533 | 47/1182 | 16/393 | chr4 | 76251793 | ||
chr4:76256200
|
G | A | 1 | a0010 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.97G>A | p.Gly33Arg | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/8 | 123/1533 | 97/1182 | 33/393 | chr4 | 76256200 | ||
chr4:76263843
|
C | T | 1 | a0008 | 1 | HG01934.hp2 | missense_variant&splice_region_variant | MODERATE | c.560C>T | p.Pro187Leu | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/8 | 586/1533 | 560/1182 | 187/393 | chr4 | 76263843 | ||
chr4:76271575
|
C | T | 1 | a0007 | 2 | NA18993.hp1 NA19089.hp1 |
missense_variant | MODERATE | c.677C>T | p.Ser226Leu | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/8 | 703/1533 | 677/1182 | 226/393 | chr4 | 76271575 | ||
chr4:76271685
|
A | C | 1 | a0003 | 53 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(50): Show |
missense_variant | MODERATE | c.787A>C | p.Lys263Gln | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/8 | 813/1533 | 787/1182 | 263/393 | chr4 | 76271685 | ||
chr4:76271715
|
G | A | 4 | a0002a0006a0009others(1): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
missense_variant | MODERATE | c.817G>A | p.Glu273Lys | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/8 | 843/1533 | 817/1182 | 273/393 | chr4 | 76271715 | ||
chr4:76280334
|
C | T | 6 | a0002a0003a0004others(3): Show | 237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
missense_variant | MODERATE | c.1097C>T | p.Thr366Met | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/8 | 1123/1533 | 1097/1182 | 366/393 | chr4 | 76280334 | ||
chr4:76283417
|
C | T | 1 | a0005 | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
missense_variant | MODERATE | c.1141C>T | p.Arg381Cys | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 8/8 | 1167/1533 | 1141/1182 | 381/393 | chr4 | 76283417 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76256262
|
C | T | 1 | a0004c0006 | 3 | HG00738.hp2 HG01361.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.159C>T | p.Asp53Asp | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/8 | 185/1533 | 159/1182 | 53/393 | chr4 | 76256262 | ||
chr4:76256418
|
G | A | 1 | a0001c0010 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.315G>A | p.Ser105Ser | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/8 | 341/1533 | 315/1182 | 105/393 | chr4 | 76256418 | ||
chr4:76280278
|
A | G | 1 | a0001c0012 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1041A>G | p.Ala347Ala | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/8 | 1067/1533 | 1041/1182 | 347/393 | chr4 | 76280278 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76283549
|
T | C | 1 | a0002c0002t0003 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 8/8 | 91 | chr4 | 76283549 | |||||
chr4:76283677
|
T | G | 2 | a0003c0003t0002a0004c0004t0002 | 3 | HG02572.hp2 HG03516.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*219T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 8/8 | 219 | chr4 | 76283677 | |||||
chr4:76283720
|
C | T | 1 | a0003c0003t0004 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 8/8 | 262 | chr4 | 76283720 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:76252138
|
C | T | 3 | a0003c0003t0001g0032a0003c0003t0001g0203a0003c0003t0001g0204 | 5 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+318C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252138 | ||||||
chr4:76252146
|
T | C | 161 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 301 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.74+326T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252146 | ||||||
chr4:76252269
|
GC | G | 11 | a0002c0002t0001g0007a0002c0002t0001g0033a0002c0002t0001g0034others(8): Show | 19 | HG00609.hp2 HG01255.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+452delC | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76252269 | |||||
chr4:76252323
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0020others(22): Show | 56 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.74+503C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252323 | ||||||
chr4:76252528
|
T | G | 1 | a0002c0002t0001g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.74+708T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252528 | ||||||
chr4:76252586
|
T | C | 10 | a0001c0001t0001g0171a0003c0003t0001g0050a0003c0003t0001g0051others(7): Show | 13 | HG00597.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.74+766T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252586 | ||||||
chr4:76252724
|
A | C | 1 | a0001c0001t0001g0202 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.74+904A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252724 | ||||||
chr4:76252761
|
C | A | 67 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0069others(64): Show | 133 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.74+941C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252761 | ||||||
chr4:76252919
|
T | C | 5 | a0002c0002t0001g0007a0002c0002t0001g0033a0002c0002t0001g0058others(2): Show | 12 | HG01255.hp1 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.74+1099T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252919 | ||||||
chr4:76252942
|
T | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0069others(53): Show | 119 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.74+1122T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252942 | ||||||
chr4:76252994
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.74+1174C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76252994 | ||||||
chr4:76253285
|
G | GGTTGTTT others(11): Show |
64 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0069others(61): Show | 129 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.74+1469_74+1486dup others(18): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76253285 | |||||
chr4:76253316
|
A | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(110): Show | 193 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.74+1496A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253316 | ||||||
chr4:76253329
|
T | C | 1 | a0003c0003t0001g0170 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.74+1509T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253329 | ||||||
chr4:76253335
|
C | T | 4 | a0003c0003t0001g0174a0005c0005t0001g0052a0005c0005t0001g0175others(1): Show | 5 | HG02723.hp1 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+1515C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253335 | ||||||
chr4:76253432
|
A | G | 1 | a0002c0002t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.74+1612A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253432 | ||||||
chr4:76253444
|
C | T | 3 | a0002c0002t0001g0019a0002c0002t0001g0185a0004c0004t0001g0184 | 6 | HG01175.hp1 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.74+1624C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253444 | ||||||
chr4:76253509
|
A | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0069others(58): Show | 125 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.74+1689A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253509 | ||||||
chr4:76253719
|
A | C | 1 | a0002c0002t0001g0097 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.74+1899A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253719 | ||||||
chr4:76253780
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.74+1960G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253780 | ||||||
chr4:76253783
|
A | C | 3 | a0002c0002t0001g0094a0002c0002t0001g0095a0004c0004t0001g0096 | 3 | HG02735.hp2 HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.74+1963A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253783 | ||||||
chr4:76253796
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.74+1976C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253796 | ||||||
chr4:76253803
|
C | G | 6 | a0003c0003t0001g0174a0005c0005t0001g0038a0005c0005t0001g0052others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+1983C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253803 | ||||||
chr4:76253808
|
T | TA | 76 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(73): Show | 138 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.74+2000dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76253808 | |||||
chr4:76253808
|
T | TAA | 33 | a0001c0001t0001g0115a0002c0002t0001g0011a0002c0002t0001g0019others(30): Show | 53 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.74+1999_74+2000dup others(2): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76253808 | |||||
chr4:76253808
|
TA | T | 9 | a0001c0001t0001g0093a0002c0002t0001g0091a0002c0002t0001g0092others(6): Show | 11 | HG02486.hp2 HG02523.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+2000delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76253808 | |||||
chr4:76253838
|
G | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0185 | 5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+2018G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253838 | ||||||
chr4:76253849
|
G | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(114): Show | 201 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.74+2029G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253849 | ||||||
chr4:76253878
|
G | A | 6 | a0003c0003t0001g0174a0005c0005t0001g0038a0005c0005t0001g0052others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2058G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253878 | ||||||
chr4:76253897
|
G | A | 6 | a0003c0003t0001g0174a0005c0005t0001g0038a0005c0005t0001g0052others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2077G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253897 | ||||||
chr4:76253936
|
A | G | 2 | a0001c0001t0001g0166a0004c0004t0001g0165 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.74+2116A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253936 | ||||||
chr4:76253955
|
C | A | 72 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(69): Show | 134 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.74+2135C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253955 | ||||||
chr4:76253959
|
A | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0020others(22): Show | 56 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.74+2139A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253959 | ||||||
chr4:76253960
|
G | A | 6 | a0003c0003t0001g0174a0005c0005t0001g0038a0005c0005t0001g0052others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2140G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253960 | ||||||
chr4:76253966
|
T | A | 5 | a0001c0001t0001g0105a0002c0002t0001g0053a0003c0003t0001g0032others(2): Show | 8 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2146T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253966 | ||||||
chr4:76253981
|
G | T | 6 | a0003c0003t0001g0174a0005c0005t0001g0038a0005c0005t0001g0052others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+2161G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76253981 | ||||||
chr4:76254092
|
T | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(114): Show | 201 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.75-2086T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254092 | ||||||
chr4:76254110
|
A | G | 6 | a0003c0003t0001g0174a0005c0005t0001g0038a0005c0005t0001g0052others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-2068A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254110 | ||||||
chr4:76254128
|
GA | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(122): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.75-2034delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76254128 | |||||
chr4:76254144
|
A | C | 6 | a0003c0003t0001g0174a0005c0005t0001g0038a0005c0005t0001g0052others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-2034A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254144 | ||||||
chr4:76254389
|
A | G | 6 | a0003c0003t0001g0174a0005c0005t0001g0038a0005c0005t0001g0052others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-1789A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254389 | ||||||
chr4:76254534
|
A | G | 24 | a0001c0001t0001g0115a0002c0002t0001g0011a0002c0002t0001g0041others(21): Show | 40 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.75-1644A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254534 | ||||||
chr4:76254542
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(62): Show | 124 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.75-1636G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254542 | ||||||
chr4:76254590
|
A | G | 38 | a0001c0001t0001g0115a0002c0002t0001g0011a0002c0002t0001g0041others(35): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.75-1588A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254590 | ||||||
chr4:76254625
|
C | T | 6 | a0003c0003t0001g0174a0005c0005t0001g0038a0005c0005t0001g0052others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-1553C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254625 | ||||||
chr4:76254813
|
G | A | 38 | a0001c0001t0001g0115a0002c0002t0001g0011a0002c0002t0001g0041others(35): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.75-1365G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254813 | ||||||
chr4:76254888
|
T | C | 1 | a0002c0002t0001g0060 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.75-1290T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254888 | ||||||
chr4:76254914
|
C | G | 1 | a0001c0001t0001g0057 | 2 | NA18988.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.75-1264C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254914 | ||||||
chr4:76254937
|
C | G | 5 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0168others(2): Show | 7 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.75-1241C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254937 | ||||||
chr4:76254942
|
G | A | 2 | a0002c0002t0001g0019a0002c0002t0001g0185 | 5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-1236G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76254942 | ||||||
chr4:76255034
|
G | A | 6 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-1144G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255034 | ||||||
chr4:76255049
|
A | G | 1 | a0002c0002t0001g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.75-1129A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255049 | ||||||
chr4:76255050
|
T | C | 1 | a0003c0003t0001g0016 | 4 | HG01884.hp1 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-1128T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255050 | ||||||
chr4:76255128
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 199 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.75-1050G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255128 | ||||||
chr4:76255136
|
A | C | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.75-1042A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255136 | ||||||
chr4:76255283
|
C | T | 1 | a0004c0004t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.75-895C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255283 | ||||||
chr4:76255356
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.75-822C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255356 | ||||||
chr4:76255371
|
T | C | 108 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0115others(105): Show | 186 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.75-807T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255371 | ||||||
chr4:76255378
|
C | G | 3 | a0003c0003t0001g0032a0003c0003t0001g0203a0003c0003t0001g0204 | 5 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-800C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255378 | ||||||
chr4:76255399
|
G | A | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 282 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.75-779G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255399 | ||||||
chr4:76255479
|
A | G | 1 | a0004c0006t0001g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.75-699A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255479 | ||||||
chr4:76255480
|
A | G | 2 | a0003c0003t0001g0040a0003c0003t0001g0103 | 3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.75-698A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255480 | ||||||
chr4:76255521
|
G | A | 38 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(35): Show | 77 | HG00423.hp1 HG00558.hp2 HG01106.hp1 others(74): Show |
intron_variant | MODIFIER | c.75-657G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255521 | ||||||
chr4:76255547
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.75-631A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255547 | ||||||
chr4:76255592
|
A | G | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.75-586A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255592 | ||||||
chr4:76255613
|
G | A | 2 | a0002c0002t0001g0019a0002c0002t0001g0185 | 5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-565G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255613 | ||||||
chr4:76255615
|
T | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 221 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.75-563T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255615 | ||||||
chr4:76255633
|
T | G | 2 | a0002c0002t0001g0019a0002c0002t0001g0185 | 5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-545T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255633 | ||||||
chr4:76255691
|
C | T | 2 | a0001c0001t0001g0156a0004c0004t0001g0126 | 2 | HG03704.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.75-487C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255691 | ||||||
chr4:76255695
|
T | C | 52 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(49): Show | 102 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.75-483T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255695 | ||||||
chr4:76255699
|
G | A | 7 | a0004c0004t0001g0114a0005c0005t0001g0038a0005c0005t0001g0052others(4): Show | 9 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.75-479G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255699 | ||||||
chr4:76255716
|
C | T | 1 | a0004c0004t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.75-462C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255716 | ||||||
chr4:76255744
|
C | T | 67 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(64): Show | 125 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.75-434C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255744 | ||||||
chr4:76255789
|
CAAG | C | 2 | a0002c0002t0001g0022a0002c0002t0001g0084 | 4 | NA18951.hp2 NA19000.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-385_75-383delAA others(1): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 76255789 | |||||
chr4:76255814
|
G | A | 7 | a0002c0002t0001g0099a0003c0003t0001g0040a0003c0003t0001g0102others(4): Show | 8 | HG02055.hp1 HG03195.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-364G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255814 | ||||||
chr4:76255874
|
A | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(32): Show | 74 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.75-304A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255874 | ||||||
chr4:76255881
|
A | G | 1 | a0002c0002t0001g0013 | 4 | HG01884.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-297A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255881 | ||||||
chr4:76255887
|
C | T | 1 | a0005c0005t0001g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.75-291C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255887 | ||||||
chr4:76255894
|
A | G | 9 | a0002c0002t0001g0019a0002c0002t0001g0099a0002c0002t0001g0185others(6): Show | 13 | HG01175.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.75-284A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255894 | ||||||
chr4:76255967
|
G | C | 7 | a0001c0001t0001g0069a0002c0002t0001g0012a0002c0002t0001g0021others(4): Show | 12 | HG02040.hp1 NA18940.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.75-211G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76255967 | ||||||
chr4:76256078
|
A | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | NA18982.hp1 NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.75-100A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 1/7 | chr4 | 76256078 | ||||||
chr4:76256664
|
A | C | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.420+141A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76256664 | ||||||
chr4:76256664
|
A | G | 103 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0115others(100): Show | 179 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.420+141A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76256664 | ||||||
chr4:76256693
|
G | A | 39 | a0001c0001t0001g0115a0002c0002t0001g0011a0002c0002t0001g0041others(36): Show | 59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.420+170G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76256693 | ||||||
chr4:76257083
|
G | A | 1 | a0003c0003t0001g0132 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.420+560G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257083 | ||||||
chr4:76257226
|
A | G | 50 | a0001c0001t0001g0171a0002c0002t0001g0011a0002c0002t0001g0041others(47): Show | 72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.420+703A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257226 | ||||||
chr4:76257257
|
G | C | 1 | a0004c0004t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.420+734G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257257 | ||||||
chr4:76257461
|
A | C | 3 | a0002c0002t0001g0099a0003c0003t0001g0040a0003c0003t0001g0103 | 4 | HG02055.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+938A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257461 | ||||||
chr4:76257529
|
C | T | 4 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0203others(1): Show | 7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.420+1006C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257529 | ||||||
chr4:76257674
|
C | T | 6 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+1151C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257674 | ||||||
chr4:76257709
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.420+1186C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257709 | ||||||
chr4:76257951
|
G | A | 3 | a0003c0003t0001g0032a0003c0003t0001g0203a0003c0003t0001g0204 | 5 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+1428G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76257951 | ||||||
chr4:76258039
|
C | G | 1 | a0004c0004t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.420+1516C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258039 | ||||||
chr4:76258339
|
G | A | 1 | a0002c0002t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.420+1816G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258339 | ||||||
chr4:76258365
|
G | T | 102 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(99): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.420+1842G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258365 | ||||||
chr4:76258448
|
T | C | 38 | a0002c0002t0001g0011a0002c0002t0001g0041a0002c0002t0001g0046others(35): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.420+1925T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258448 | ||||||
chr4:76258499
|
A | C | 6 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+1976A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258499 | ||||||
chr4:76258538
|
G | A | 1 | a0004c0004t0001g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.420+2015G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258538 | ||||||
chr4:76258563
|
T | C | 8 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0102others(5): Show | 11 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.420+2040T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258563 | ||||||
chr4:76258598
|
T | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.420+2075T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258598 | ||||||
chr4:76258677
|
C | T | 55 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(52): Show | 107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.420+2154C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258677 | ||||||
chr4:76258745
|
C | T | 55 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(52): Show | 107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.420+2222C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258745 | ||||||
chr4:76258832
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.420+2309T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258832 | ||||||
chr4:76258992
|
T | C | 55 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(52): Show | 107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.420+2469T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76258992 | ||||||
chr4:76259017
|
A | G | 1 | a0002c0002t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.420+2494A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259017 | ||||||
chr4:76259051
|
G | T | 1 | a0002c0002t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.420+2528G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259051 | ||||||
chr4:76259062
|
C | T | 1 | a0004c0004t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.420+2539C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259062 | ||||||
chr4:76259408
|
G | A | 4 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0203others(1): Show | 7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.420+2885G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259408 | ||||||
chr4:76259459
|
G | A | 102 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(99): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.420+2936G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259459 | ||||||
chr4:76259514
|
C | A | 1 | a0004c0004t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.420+2991C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259514 | ||||||
chr4:76259663
|
T | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(31): Show | 72 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.420+3140T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259663 | ||||||
chr4:76259667
|
C | T | 1 | a0003c0003t0001g0173 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.420+3144C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259667 | ||||||
chr4:76259781
|
A | G | 1 | a0002c0002t0001g0125 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.420+3258A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259781 | ||||||
chr4:76259787
|
A | C | 104 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0105others(101): Show | 179 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.420+3264A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259787 | ||||||
chr4:76259864
|
A | AGG | 4 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0203others(1): Show | 7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.420+3342_420+3343i others(4): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 76259864 | |||||
chr4:76259980
|
A | G | 1 | a0001c0001t0001g0029 | 3 | HG02698.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.420+3457A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76259980 | ||||||
chr4:76260170
|
G | A | 102 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(99): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.421-3534G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260170 | ||||||
chr4:76260284
|
G | A | 102 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(99): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.421-3420G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260284 | ||||||
chr4:76260383
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.421-3321A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260383 | ||||||
chr4:76260391
|
T | G | 102 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(99): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.421-3313T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260391 | ||||||
chr4:76260549
|
A | G | 6 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-3155A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260549 | ||||||
chr4:76260559
|
TAACTC | T | 55 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(52): Show | 107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-3142_421-3138d others(7): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 76260559 | |||||
chr4:76260602
|
A | G | 55 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(52): Show | 107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-3102A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260602 | ||||||
chr4:76260786
|
A | G | 55 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(52): Show | 107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-2918A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260786 | ||||||
chr4:76260824
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.421-2880G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260824 | ||||||
chr4:76260830
|
T | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0185 | 5 | HG01175.hp1 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-2874T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260830 | ||||||
chr4:76260851
|
G | T | 102 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(99): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.421-2853G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260851 | ||||||
chr4:76260859
|
T | C | 42 | a0002c0002t0001g0011a0002c0002t0001g0041a0002c0002t0001g0046others(39): Show | 62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.421-2845T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260859 | ||||||
chr4:76260880
|
T | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 276 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.421-2824T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76260880 | ||||||
chr4:76260983
|
C | CA | 8 | a0001c0001t0001g0130a0002c0002t0001g0019a0002c0002t0001g0053others(5): Show | 12 | HG01175.hp1 HG02258.hp2 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-2708dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 76260983 | |||||
chr4:76261037
|
A | C | 1 | a0002c0002t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421-2667A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261037 | ||||||
chr4:76261120
|
C | T | 55 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(52): Show | 107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-2584C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261120 | ||||||
chr4:76261256
|
A | G | 55 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(52): Show | 107 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.421-2448A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261256 | ||||||
chr4:76261325
|
A | G | 1 | a0002c0002t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421-2379A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261325 | ||||||
chr4:76261523
|
G | A | 2 | a0002c0002t0001g0179a0002c0002t0001g0191 | 2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.421-2181G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261523 | ||||||
chr4:76261525
|
C | T | 4 | a0003c0003t0001g0102a0003c0003t0001g0174a0003c0003t0002g0100others(1): Show | 4 | HG03195.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-2179C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261525 | ||||||
chr4:76261527
|
T | C | 1 | a0003c0003t0001g0174 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.421-2177T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261527 | ||||||
chr4:76261573
|
A | G | 102 | a0001c0001t0001g0069a0001c0001t0001g0093a0002c0002t0001g0001others(99): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.421-2131A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261573 | ||||||
chr4:76261677
|
G | A | 4 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0203others(1): Show | 7 | HG02572.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-2027G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76261677 | ||||||
chr4:76262147
|
A | C | 38 | a0002c0002t0001g0019a0002c0002t0001g0099a0002c0002t0001g0179others(35): Show | 56 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.421-1557A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262147 | ||||||
chr4:76262148
|
A | G | 7 | a0004c0004t0001g0024a0005c0005t0001g0038a0005c0005t0001g0052others(4): Show | 11 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-1556A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262148 | ||||||
chr4:76262176
|
A | T | 1 | a0003c0003t0001g0051 | 2 | NA18988.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.421-1528A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262176 | ||||||
chr4:76262251
|
C | A | 1 | a0002c0002t0001g0061 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.421-1453C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262251 | ||||||
chr4:76262267
|
G | A | 1 | a0001c0001t0001g0057 | 2 | NA18988.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.421-1437G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262267 | ||||||
chr4:76262272
|
T | C | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.421-1432T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262272 | ||||||
chr4:76262281
|
T | C | 38 | a0002c0002t0001g0019a0002c0002t0001g0099a0002c0002t0001g0179others(35): Show | 56 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.421-1423T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262281 | ||||||
chr4:76262423
|
C | T | 1 | a0001c0001t0001g0044 | 2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.421-1281C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262423 | ||||||
chr4:76262493
|
A | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(39): Show | 92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.421-1211A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262493 | ||||||
chr4:76262713
|
A | G | 1 | a0004c0004t0001g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.421-991A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262713 | ||||||
chr4:76262724
|
T | C | 3 | a0002c0002t0001g0099a0003c0003t0001g0040a0003c0003t0001g0103 | 4 | HG02055.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-980T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262724 | ||||||
chr4:76262778
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(39): Show | 92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.421-926T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262778 | ||||||
chr4:76262876
|
C | G | 6 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-828C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262876 | ||||||
chr4:76262939
|
T | A | 8 | a0002c0002t0001g0053a0002c0002t0001g0098a0003c0003t0001g0032others(5): Show | 11 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-765T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76262939 | ||||||
chr4:76262943
|
TTAAATAG others(189): Show |
T | 1 | a0005c0005t0001g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.421-756_421-561del | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 76262943 | |||||
chr4:76263031
|
C | T | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.421-673C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263031 | ||||||
chr4:76263184
|
A | G | 1 | a0003c0003t0001g0050 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.421-520A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263184 | ||||||
chr4:76263191
|
T | C | 1 | a0006c0007t0001g0073 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.421-513T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263191 | ||||||
chr4:76263242
|
G | C | 109 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(106): Show | 188 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.421-462G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263242 | ||||||
chr4:76263380
|
T | G | 1 | a0001c0001t0001g0153 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.421-324T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263380 | ||||||
chr4:76263402
|
T | C | 5 | a0002c0002t0001g0019a0002c0002t0001g0098a0002c0002t0001g0179others(2): Show | 8 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-302T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 2/7 | chr4 | 76263402 | ||||||
chr4:76263844
|
G | A | 6 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0071others(3): Show | 9 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
splice_donor_variant&intron_variant | HIGH | c.560+1G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76263844 | ||||||
chr4:76263844
|
G | C | 3 | a0002c0002t0001g0035a0002c0002t0001g0074a0002c0002t0001g0140 | 4 | NA18957.hp2 NA19063.hp2 NA19067.hp2 others(1): Show |
splice_donor_variant&intron_variant | HIGH | c.560+1G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76263844 | ||||||
chr4:76263898
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.560+55G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76263898 | ||||||
chr4:76263993
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.560+150C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76263993 | ||||||
chr4:76264023
|
A | T | 19 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(16): Show | 37 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.560+180A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264023 | ||||||
chr4:76264041
|
C | T | 19 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(16): Show | 37 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.560+198C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264041 | ||||||
chr4:76264056
|
C | T | 3 | a0001c0001t0001g0105a0004c0004t0001g0114a0004c0004t0001g0184 | 3 | HG02965.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.560+213C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264056 | ||||||
chr4:76264140
|
G | A | 70 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(67): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.560+297G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264140 | ||||||
chr4:76264206
|
T | C | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.560+363T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264206 | ||||||
chr4:76264213
|
A | G | 1 | a0001c0001t0001g0018 | 4 | HG01070.hp2 HG01361.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+370A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264213 | ||||||
chr4:76264376
|
G | C | 64 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(61): Show | 121 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.560+533G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264376 | ||||||
chr4:76264547
|
G | A | 3 | a0001c0001t0001g0105a0004c0004t0001g0114a0004c0004t0001g0184 | 3 | HG02965.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.560+704G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264547 | ||||||
chr4:76264552
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.560+709G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264552 | ||||||
chr4:76264726
|
A | G | 31 | a0003c0003t0001g0102a0003c0003t0002g0100a0004c0004t0001g0008others(28): Show | 45 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.560+883A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264726 | ||||||
chr4:76264747
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.560+904C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264747 | ||||||
chr4:76264795
|
C | T | 1 | a0003c0003t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+952C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264795 | ||||||
chr4:76264844
|
C | T | 70 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(67): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.560+1001C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264844 | ||||||
chr4:76264947
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.560+1104G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76264947 | ||||||
chr4:76265099
|
A | T | 1 | a0004c0004t0001g0014 | 4 | HG00642.hp2 HG00741.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+1256A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265099 | ||||||
chr4:76265262
|
A | C | 71 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(68): Show | 132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.560+1419A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265262 | ||||||
chr4:76265277
|
C | T | 3 | a0003c0003t0001g0102a0003c0003t0002g0100a0004c0004t0002g0101 | 3 | HG03486.hp2 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.560+1434C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265277 | ||||||
chr4:76265294
|
G | A | 2 | a0002c0002t0001g0116a0002c0002t0001g0117 | 2 | HG01081.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.560+1451G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265294 | ||||||
chr4:76265424
|
A | G | 1 | a0001c0001t0001g0057 | 2 | NA18988.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.560+1581A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265424 | ||||||
chr4:76265434
|
C | T | 3 | a0001c0001t0001g0105a0004c0004t0001g0114a0004c0004t0001g0184 | 3 | HG02965.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.560+1591C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265434 | ||||||
chr4:76265443
|
C | G | 64 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(61): Show | 122 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.560+1600C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265443 | ||||||
chr4:76265489
|
G | A | 31 | a0003c0003t0001g0102a0003c0003t0002g0100a0004c0004t0001g0008others(28): Show | 45 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.560+1646G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265489 | ||||||
chr4:76265519
|
T | C | 71 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(68): Show | 132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.560+1676T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265519 | ||||||
chr4:76265609
|
T | TTATTCAT others(1): Show |
110 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(107): Show | 189 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.560+1767_560+1774d others(10): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 76265609 | |||||
chr4:76265659
|
T | C | 110 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(107): Show | 189 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.560+1816T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265659 | ||||||
chr4:76265660
|
G | A | 2 | a0003c0003t0001g0040a0003c0003t0001g0103 | 3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.560+1817G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265660 | ||||||
chr4:76265683
|
G | A | 1 | a0002c0002t0001g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560+1840G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265683 | ||||||
chr4:76265771
|
A | C | 102 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(99): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.560+1928A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265771 | ||||||
chr4:76265781
|
C | T | 2 | a0001c0001t0001g0105a0004c0004t0001g0114 | 2 | HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.560+1938C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265781 | ||||||
chr4:76265868
|
C | T | 1 | a0003c0003t0001g0072 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.560+2025C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265868 | ||||||
chr4:76265879
|
T | C | 102 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(99): Show | 177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.560+2036T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76265879 | ||||||
chr4:76265947
|
T | TA | 42 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(39): Show | 92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.560+2105dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 76265947 | |||||
chr4:76266070
|
G | C | 7 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0071others(4): Show | 10 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.560+2227G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266070 | ||||||
chr4:76266143
|
G | A | 4 | a0003c0003t0001g0102a0003c0003t0002g0100a0004c0004t0001g0165others(1): Show | 4 | HG03486.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.560+2300G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266143 | ||||||
chr4:76266160
|
T | C | 1 | a0004c0004t0001g0109 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.560+2317T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266160 | ||||||
chr4:76266328
|
C | T | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.561-2332C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266328 | ||||||
chr4:76266403
|
G | A | 71 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(68): Show | 132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.561-2257G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266403 | ||||||
chr4:76266473
|
A | G | 110 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(107): Show | 189 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.561-2187A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266473 | ||||||
chr4:76266517
|
T | C | 1 | a0004c0004t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.561-2143T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266517 | ||||||
chr4:76266668
|
G | A | 3 | a0003c0003t0001g0040a0003c0003t0001g0103a0004c0004t0002g0101 | 4 | HG03516.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-1992G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266668 | ||||||
chr4:76266726
|
T | C | 2 | a0003c0003t0001g0040a0003c0003t0001g0103 | 3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1934T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266726 | ||||||
chr4:76266763
|
C | T | 39 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0040others(36): Show | 57 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.561-1897C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266763 | ||||||
chr4:76266905
|
A | G | 39 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0040others(36): Show | 57 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.561-1755A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266905 | ||||||
chr4:76266967
|
T | C | 3 | a0001c0001t0001g0105a0004c0004t0001g0114a0004c0004t0001g0184 | 3 | HG02965.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.561-1693T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266967 | ||||||
chr4:76266979
|
A | G | 66 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(63): Show | 124 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.561-1681A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76266979 | ||||||
chr4:76267021
|
TCC | T | 39 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0040others(36): Show | 57 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.561-1635_561-1634d others(4): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 76267021 | |||||
chr4:76267087
|
A | G | 71 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(68): Show | 132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.561-1573A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267087 | ||||||
chr4:76267091
|
G | A | 110 | a0001c0001t0001g0069a0002c0002t0001g0001a0002c0002t0001g0004others(107): Show | 189 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.561-1569G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267091 | ||||||
chr4:76267124
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0198 | 5 | NA18945.hp2 NA18970.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-1536C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267124 | ||||||
chr4:76267135
|
G | C | 39 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0040others(36): Show | 57 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.561-1525G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267135 | ||||||
chr4:76267174
|
T | G | 39 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0040others(36): Show | 57 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.561-1486T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267174 | ||||||
chr4:76267186
|
A | T | 21 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(18): Show | 40 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.561-1474A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267186 | ||||||
chr4:76267218
|
T | C | 2 | a0003c0003t0001g0040a0003c0003t0001g0103 | 3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1442T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267218 | ||||||
chr4:76267223
|
G | A | 1 | a0004c0004t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.561-1437G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267223 | ||||||
chr4:76267251
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.561-1409T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267251 | ||||||
chr4:76267265
|
C | G | 39 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0040others(36): Show | 57 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.561-1395C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267265 | ||||||
chr4:76267330
|
G | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0086others(4): Show | 19 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.561-1330G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267330 | ||||||
chr4:76267460
|
T | C | 115 | a0001c0001t0001g0069a0001c0001t0001g0162a0001c0001t0001g0163others(112): Show | 195 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.561-1200T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267460 | ||||||
chr4:76267613
|
A | T | 39 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0040others(36): Show | 57 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.561-1047A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267613 | ||||||
chr4:76267753
|
A | G | 1 | a0002c0002t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.561-907A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76267753 | ||||||
chr4:76268119
|
G | C | 2 | a0003c0003t0001g0102a0004c0004t0002g0101 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.561-541G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268119 | ||||||
chr4:76268227
|
A | G | 37 | a0002c0002t0001g0053a0003c0003t0001g0032a0003c0003t0001g0071others(34): Show | 54 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.561-433A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268227 | ||||||
chr4:76268265
|
C | T | 36 | a0003c0003t0001g0032a0003c0003t0001g0040a0003c0003t0001g0071others(33): Show | 53 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.561-395C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268265 | ||||||
chr4:76268408
|
T | A | 1 | a0002c0002t0001g0062 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.561-252T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268408 | ||||||
chr4:76268409
|
A | T | 1 | a0002c0002t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.561-251A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268409 | ||||||
chr4:76268460
|
C | A | 5 | a0003c0003t0001g0032a0003c0003t0001g0071a0003c0003t0001g0072others(2): Show | 7 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.561-200C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 3/7 | chr4 | 76268460 | ||||||
chr4:76268830
|
A | G | 2 | a0003c0003t0001g0040a0003c0003t0001g0103 | 3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.669+62A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76268830 | ||||||
chr4:76268831
|
T | C | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+63T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76268831 | ||||||
chr4:76268916
|
C | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+148C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76268916 | ||||||
chr4:76269068
|
T | A | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+300T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269068 | ||||||
chr4:76269116
|
T | C | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+348T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269116 | ||||||
chr4:76269194
|
G | A | 6 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+426G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269194 | ||||||
chr4:76269240
|
C | T | 1 | a0002c0002t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.669+472C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269240 | ||||||
chr4:76269245
|
A | G | 125 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(122): Show | 222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.669+477A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269245 | ||||||
chr4:76269343
|
G | A | 1 | a0002c0002t0001g0077 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.669+575G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269343 | ||||||
chr4:76269496
|
A | G | 31 | a0003c0003t0001g0102a0003c0003t0002g0100a0004c0004t0001g0008others(28): Show | 45 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.669+728A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269496 | ||||||
chr4:76269527
|
G | A | 65 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(62): Show | 123 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.669+759G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269527 | ||||||
chr4:76269580
|
T | C | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+812T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269580 | ||||||
chr4:76269621
|
A | ATATAT | 6 | a0002c0002t0001g0019a0002c0002t0001g0053a0002c0002t0001g0054others(3): Show | 11 | HG01175.hp1 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.669+853_669+854ins others(5): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269621 | ||||||
chr4:76269621
|
A | ATATATAA others(2): Show |
66 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(63): Show | 124 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.669+853_669+854ins others(9): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269621 | ||||||
chr4:76269623
|
T | A | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+855T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269623 | ||||||
chr4:76269720
|
C | A | 2 | a0003c0003t0001g0040a0003c0003t0001g0103 | 3 | NA18522.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.669+952C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269720 | ||||||
chr4:76269749
|
T | C | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+981T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269749 | ||||||
chr4:76269779
|
T | C | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1011T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269779 | ||||||
chr4:76269787
|
C | CA | 115 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0023others(112): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.669+1032dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 76269787 | |||||
chr4:76269787
|
CA | C | 5 | a0003c0003t0001g0032a0003c0003t0001g0071a0003c0003t0001g0072others(2): Show | 7 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+1032delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 76269787 | |||||
chr4:76269850
|
G | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1082G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269850 | ||||||
chr4:76269896
|
T | C | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1128T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269896 | ||||||
chr4:76269959
|
T | C | 134 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(131): Show | 233 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.669+1191T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269959 | ||||||
chr4:76269990
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.669+1222G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76269990 | ||||||
chr4:76270107
|
A | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1339A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270107 | ||||||
chr4:76270163
|
T | C | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.669+1395T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270163 | ||||||
chr4:76270202
|
TC | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-1362delC | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 76270202 | |||||
chr4:76270269
|
G | A | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-1299G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270269 | ||||||
chr4:76270443
|
A | G | 66 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(63): Show | 125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.670-1125A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270443 | ||||||
chr4:76270564
|
T | C | 1 | a0002c0002t0001g0137 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.670-1004T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270564 | ||||||
chr4:76270768
|
C | A | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-800C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270768 | ||||||
chr4:76270799
|
G | A | 29 | a0004c0004t0001g0008a0004c0004t0001g0014a0004c0004t0001g0024others(26): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.670-769G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270799 | ||||||
chr4:76270910
|
T | G | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-658T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270910 | ||||||
chr4:76270926
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.670-642A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76270926 | ||||||
chr4:76271039
|
T | C | 1 | a0004c0004t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.670-529T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271039 | ||||||
chr4:76271235
|
T | G | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-333T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271235 | ||||||
chr4:76271339
|
C | T | 1 | a0002c0002t0001g0037 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.670-229C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271339 | ||||||
chr4:76271359
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.670-209C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271359 | ||||||
chr4:76271459
|
A | T | 1 | a0004c0004t0001g0158 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.670-109A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271459 | ||||||
chr4:76271469
|
A | T | 1 | a0004c0004t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.670-99A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271469 | ||||||
chr4:76271535
|
G | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.670-33G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 4/7 | chr4 | 76271535 | ||||||
chr4:76271793
|
G | A | 1 | a0002c0002t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.870+25G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271793 | ||||||
chr4:76271854
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0130 | 5 | NA18946.hp2 NA18981.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.870+86G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271854 | ||||||
chr4:76271880
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.870+112C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271880 | ||||||
chr4:76271894
|
A | G | 6 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+126A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271894 | ||||||
chr4:76271904
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.870+136T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271904 | ||||||
chr4:76271942
|
T | G | 1 | a0002c0002t0001g0033 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.870+174T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271942 | ||||||
chr4:76271983
|
A | G | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+215A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76271983 | ||||||
chr4:76272055
|
A | T | 21 | a0004c0004t0001g0008a0004c0004t0001g0014a0004c0004t0001g0024others(18): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.870+287A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272055 | ||||||
chr4:76272075
|
T | C | 2 | a0003c0003t0001g0049a0003c0003t0001g0134 | 3 | HG01516.hp2 HG02647.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.870+307T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272075 | ||||||
chr4:76272296
|
T | C | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+528T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272296 | ||||||
chr4:76272392
|
T | G | 134 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(131): Show | 233 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.870+624T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272392 | ||||||
chr4:76272413
|
C | T | 1 | a0001c0001t0001g0017 | 4 | NA18942.hp1 NA18943.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+645C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272413 | ||||||
chr4:76272437
|
A | G | 1 | a0003c0003t0001g0050 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.870+669A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272437 | ||||||
chr4:76272496
|
T | A | 21 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(18): Show | 40 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.870+728T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272496 | ||||||
chr4:76272575
|
T | G | 134 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(131): Show | 233 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.870+807T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272575 | ||||||
chr4:76272589
|
C | A | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+821C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272589 | ||||||
chr4:76272782
|
T | G | 1 | a0001c0001t0001g0031 | 3 | HG02165.hp1 HG03834.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.870+1014T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272782 | ||||||
chr4:76272893
|
A | G | 6 | a0003c0003t0001g0032a0003c0003t0001g0071a0003c0003t0001g0072others(3): Show | 8 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+1125A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272893 | ||||||
chr4:76272911
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.870+1143A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272911 | ||||||
chr4:76272939
|
G | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1171G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272939 | ||||||
chr4:76272993
|
G | T | 1 | a0001c0001t0001g0055 | 2 | HG01106.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.870+1225G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76272993 | ||||||
chr4:76273068
|
A | G | 5 | a0002c0002t0001g0019a0002c0002t0001g0053a0002c0002t0001g0098others(2): Show | 9 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.870+1300A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273068 | ||||||
chr4:76273070
|
T | C | 1 | a0001c0001t0001g0029 | 3 | HG02698.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.870+1302T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273070 | ||||||
chr4:76273093
|
G | A | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1325G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273093 | ||||||
chr4:76273119
|
T | C | 1 | a0001c0001t0001g0029 | 3 | HG02698.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.870+1351T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273119 | ||||||
chr4:76273158
|
G | C | 1 | a0003c0003t0001g0173 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.870+1390G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273158 | ||||||
chr4:76273159
|
G | T | 1 | a0003c0003t0001g0173 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.870+1391G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273159 | ||||||
chr4:76273320
|
G | A | 127 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(124): Show | 222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.870+1552G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273320 | ||||||
chr4:76273448
|
GCCTT | G | 3 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0176 | 5 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.870+1684_870+1687d others(6): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76273448 | |||||
chr4:76273511
|
T | G | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1743T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273511 | ||||||
chr4:76273517
|
G | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1749G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273517 | ||||||
chr4:76273524
|
C | G | 1 | a0005c0005t0001g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.870+1756C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273524 | ||||||
chr4:76273531
|
C | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1763C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273531 | ||||||
chr4:76273650
|
G | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(37): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.870+1882G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273650 | ||||||
chr4:76273728
|
C | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+1960C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273728 | ||||||
chr4:76273844
|
G | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+2076G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273844 | ||||||
chr4:76273856
|
A | AT | 71 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(68): Show | 134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.870+2097dupT | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76273856 | |||||
chr4:76273920
|
T | C | 5 | a0002c0002t0001g0019a0002c0002t0001g0053a0002c0002t0001g0098others(2): Show | 9 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.870+2152T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273920 | ||||||
chr4:76273953
|
G | C | 23 | a0004c0004t0001g0008a0004c0004t0001g0014a0004c0004t0001g0024others(20): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.870+2185G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273953 | ||||||
chr4:76273957
|
T | C | 28 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(25): Show | 49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.870+2189T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76273957 | ||||||
chr4:76274165
|
C | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+2397C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274165 | ||||||
chr4:76274380
|
C | T | 1 | a0004c0004t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.870+2612C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274380 | ||||||
chr4:76274389
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.870+2621T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274389 | ||||||
chr4:76274409
|
C | CA | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+2650dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76274409 | |||||
chr4:76274579
|
T | C | 76 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(73): Show | 147 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.870+2811T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274579 | ||||||
chr4:76274837
|
C | A | 1 | a0003c0003t0001g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.870+3069C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274837 | ||||||
chr4:76274881
|
T | C | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.870+3113T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274881 | ||||||
chr4:76274953
|
C | T | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.871-3116C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274953 | ||||||
chr4:76274990
|
C | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(37): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.871-3079C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76274990 | ||||||
chr4:76275035
|
T | C | 29 | a0004c0004t0001g0008a0004c0004t0001g0014a0004c0004t0001g0024others(26): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.871-3034T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275035 | ||||||
chr4:76275067
|
A | AT | 22 | a0004c0004t0001g0008a0004c0004t0001g0014a0004c0004t0001g0024others(19): Show | 34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.871-2996dupT | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76275067 | |||||
chr4:76275294
|
T | C | 2 | a0003c0003t0001g0042a0003c0003t0001g0133 | 3 | NA18948.hp2 NA18954.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.871-2775T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275294 | ||||||
chr4:76275323
|
T | G | 21 | a0004c0004t0001g0008a0004c0004t0001g0014a0004c0004t0001g0024others(18): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.871-2746T>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275323 | ||||||
chr4:76275347
|
C | T | 67 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(64): Show | 126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.871-2722C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275347 | ||||||
chr4:76275426
|
C | T | 2 | a0003c0003t0001g0030a0003c0003t0002g0161 | 4 | HG02572.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2643C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275426 | ||||||
chr4:76275519
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.871-2550A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275519 | ||||||
chr4:76275524
|
G | A | 60 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(57): Show | 96 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.871-2545G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275524 | ||||||
chr4:76275695
|
A | G | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.871-2374A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275695 | ||||||
chr4:76275862
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(207): Show | 391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.871-2207A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275862 | ||||||
chr4:76275872
|
G | T | 1 | a0002c0002t0001g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.871-2197G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76275872 | ||||||
chr4:76276029
|
GACAGACA others(9): Show |
G | 33 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(30): Show | 56 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.871-2036_871-2021d others(18): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276029 | |||||
chr4:76276033
|
G | GACACACA others(3): Show |
1 | a0004c0004t0001g0144 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.871-2033_871-2032i others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276033 | |||||
chr4:76276033
|
GACAGACA others(7): Show |
G | 3 | a0003c0003t0001g0040a0003c0003t0001g0103a0003c0003t0001g0187 | 4 | NA18522.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2032_871-2019d others(16): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276033 | |||||
chr4:76276033
|
GACAGACA others(9): Show |
G | 24 | a0003c0003t0002g0100a0004c0004t0001g0008a0004c0004t0001g0014others(21): Show | 36 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.871-2032_871-2017d others(18): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276033 | |||||
chr4:76276037
|
G | C | 5 | a0001c0001t0001g0154a0002c0002t0001g0061a0002c0002t0001g0062others(2): Show | 5 | HG00609.hp2 HG01069.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.871-2032G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276037 | ||||||
chr4:76276037
|
G | GAC | 4 | a0001c0001t0001g0056a0001c0001t0001g0115a0001c0001t0001g0194others(1): Show | 5 | HG00642.hp1 HG01255.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-2001_871-2000d others(4): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | |||||
chr4:76276037
|
G | GACAC | 37 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(34): Show | 92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-2003_871-2000d others(6): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | |||||
chr4:76276037
|
G | GACACAC | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0167others(6): Show | 13 | HG01884.hp2 HG02055.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.871-2005_871-2000d others(8): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | |||||
chr4:76276037
|
G | GACACACA others(1): Show |
17 | a0002c0002t0001g0004a0002c0002t0001g0011a0002c0002t0001g0034others(14): Show | 35 | HG00140.hp2 HG01433.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.871-2007_871-2000d others(10): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | |||||
chr4:76276037
|
G | GACACACA others(3): Show |
20 | a0001c0001t0001g0105a0002c0002t0001g0001a0002c0002t0001g0012others(17): Show | 49 | HG00423.hp1 HG00558.hp2 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.871-2009_871-2000d others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | |||||
chr4:76276037
|
G | GACACACA others(5): Show |
8 | a0002c0002t0001g0036a0002c0002t0001g0082a0002c0002t0001g0084others(5): Show | 9 | HG01081.hp1 HG01258.hp1 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.871-2011_871-2000d others(14): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | |||||
chr4:76276037
|
G | GACAGACA others(1): Show |
8 | a0001c0001t0001g0150a0002c0002t0001g0019a0002c0002t0001g0041others(5): Show | 13 | HG00735.hp2 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.871-2029_871-2028i others(10): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | |||||
chr4:76276037
|
G | GACAGACA others(3): Show |
1 | a0002c0002t0001g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.871-2029_871-2028i others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | |||||
chr4:76276037
|
G | GACAGACA others(3): Show |
1 | a0002c0002t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.871-2029_871-2028i others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276037 | |||||
chr4:76276070
|
C | A | 69 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(66): Show | 130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.871-1999C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276070 | ||||||
chr4:76276071
|
C | A | 1 | a0002c0002t0001g0064 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.871-1998C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276071 | ||||||
chr4:76276073
|
T | C | 1 | a0002c0002t0001g0064 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.871-1996T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276073 | ||||||
chr4:76276074
|
C | T | 1 | a0002c0002t0001g0064 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.871-1995C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276074 | ||||||
chr4:76276077
|
C | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0085 | 4 | NA18939.hp2 NA18941.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-1992C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276077 | ||||||
chr4:76276231
|
T | C | 1 | a0002c0002t0001g0043 | 2 | NA18961.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.871-1838T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276231 | ||||||
chr4:76276243
|
C | T | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-1826C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276243 | ||||||
chr4:76276244
|
A | G | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-1825A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276244 | ||||||
chr4:76276285
|
GA | G | 5 | a0002c0002t0001g0019a0002c0002t0001g0053a0002c0002t0001g0098others(2): Show | 9 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-1781delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276285 | |||||
chr4:76276355
|
C | CTTTTTGT others(3): Show |
27 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(24): Show | 48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.871-1709_871-1708i others(12): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276355 | |||||
chr4:76276355
|
C | CTTTTTGT others(4): Show |
7 | a0004c0004t0001g0165a0005c0005t0001g0038a0005c0005t0001g0052others(4): Show | 9 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-1709_871-1708i others(13): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276355 | |||||
chr4:76276356
|
T | TTTTTGTT others(21): Show |
1 | a0004c0004t0001g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.871-1709_871-1708i others(30): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276356 | |||||
chr4:76276356
|
T | TTTTTGTT others(12): Show |
1 | a0004c0004t0001g0110 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.871-1709_871-1708i others(21): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276356 | |||||
chr4:76276356
|
T | TTTTTGTT others(21): Show |
21 | a0003c0003t0002g0100a0004c0004t0001g0008a0004c0004t0001g0014others(18): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.871-1709_871-1708i others(30): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276356 | |||||
chr4:76276364
|
G | GT | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-1702dupT | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276364 | |||||
chr4:76276368
|
G | GTTTGTTT others(1): Show |
70 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(67): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.871-1693_871-1686d others(10): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276368 | |||||
chr4:76276368
|
G | T | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-1701G>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276368 | ||||||
chr4:76276384
|
A | T | 174 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 322 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.871-1685A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276384 | ||||||
chr4:76276397
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.871-1672G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276397 | ||||||
chr4:76276411
|
C | T | 1 | a0004c0004t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.871-1658C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276411 | ||||||
chr4:76276434
|
G | A | 2 | a0001c0001t0001g0152a0002c0002t0001g0080 | 2 | HG00423.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.871-1635G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276434 | ||||||
chr4:76276498
|
G | A | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-1571G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276498 | ||||||
chr4:76276518
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.871-1551A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276518 | ||||||
chr4:76276521
|
C | T | 58 | a0001c0001t0001g0105a0003c0003t0001g0009a0003c0003t0001g0016others(55): Show | 93 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.871-1548C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276521 | ||||||
chr4:76276588
|
CCCAA | C | 68 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(65): Show | 128 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.871-1478_871-1475d others(6): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76276588 | |||||
chr4:76276692
|
A | G | 31 | a0003c0003t0001g0102a0003c0003t0002g0100a0004c0004t0001g0008others(28): Show | 45 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.871-1377A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276692 | ||||||
chr4:76276729
|
G | C | 70 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(67): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.871-1340G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276729 | ||||||
chr4:76276901
|
C | T | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-1168C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276901 | ||||||
chr4:76276913
|
G | A | 5 | a0003c0003t0001g0032a0003c0003t0001g0071a0003c0003t0001g0072others(2): Show | 7 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-1156G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76276913 | ||||||
chr4:76277077
|
T | C | 2 | a0002c0002t0001g0036a0002c0002t0001g0082 | 3 | NA18947.hp2 NA19056.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.871-992T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277077 | ||||||
chr4:76277210
|
C | T | 21 | a0004c0004t0001g0008a0004c0004t0001g0014a0004c0004t0001g0024others(18): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.871-859C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277210 | ||||||
chr4:76277211
|
G | A | 1 | a0003c0003t0001g0133 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.871-858G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277211 | ||||||
chr4:76277266
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0147 | 4 | HG00609.hp1 NA18952.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-803C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277266 | ||||||
chr4:76277312
|
G | A | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-757G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277312 | ||||||
chr4:76277413
|
G | A | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-656G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277413 | ||||||
chr4:76277418
|
G | A | 71 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(68): Show | 133 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.871-651G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277418 | ||||||
chr4:76277434
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.871-635C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277434 | ||||||
chr4:76277484
|
C | T | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-585C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277484 | ||||||
chr4:76277489
|
C | G | 5 | a0003c0003t0001g0032a0003c0003t0001g0071a0003c0003t0001g0072others(2): Show | 7 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.871-580C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277489 | ||||||
chr4:76277509
|
GA | G | 2 | a0002c0002t0001g0012a0002c0002t0001g0067 | 5 | NA18946.hp1 NA18952.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-550delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76277509 | |||||
chr4:76277547
|
T | TA | 33 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(30): Show | 56 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.871-511dupA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76277547 | |||||
chr4:76277547
|
TA | T | 21 | a0004c0004t0001g0008a0004c0004t0001g0014a0004c0004t0001g0024others(18): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.871-511delA | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 76277547 | |||||
chr4:76277603
|
A | G | 174 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 322 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.871-466A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277603 | ||||||
chr4:76277635
|
A | G | 3 | a0002c0002t0001g0019a0002c0002t0001g0179a0002c0002t0001g0191 | 6 | HG01175.hp1 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.871-434A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277635 | ||||||
chr4:76277638
|
G | A | 73 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(70): Show | 135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.871-431G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277638 | ||||||
chr4:76277758
|
C | T | 2 | a0003c0003t0002g0100a0004c0004t0002g0101 | 2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.871-311C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277758 | ||||||
chr4:76277833
|
C | T | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.871-236C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277833 | ||||||
chr4:76277953
|
A | G | 1 | a0004c0004t0001g0122 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.871-116A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277953 | ||||||
chr4:76277986
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.871-83C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76277986 | ||||||
chr4:76278058
|
A | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(27): Show | 65 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.871-11A>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 5/7 | chr4 | 76278058 | ||||||
chr4:76278261
|
C | A | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1026+37C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278261 | ||||||
chr4:76278309
|
G | A | 2 | a0003c0003t0002g0100a0004c0004t0002g0101 | 2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1026+85G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278309 | ||||||
chr4:76278338
|
C | T | 2 | a0003c0003t0001g0103a0003c0003t0001g0187 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1026+114C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278338 | ||||||
chr4:76278548
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0201 | 2 | HG00544.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1026+324C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278548 | ||||||
chr4:76278751
|
A | G | 131 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(128): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1026+527A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278751 | ||||||
chr4:76278760
|
G | A | 57 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(54): Show | 92 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1026+536G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278760 | ||||||
chr4:76278788
|
C | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1026+564C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76278788 | ||||||
chr4:76279503
|
T | C | 1 | a0002c0002t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1027-761T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279503 | ||||||
chr4:76279646
|
C | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1027-618C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279646 | ||||||
chr4:76279652
|
C | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1027-612C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279652 | ||||||
chr4:76279664
|
C | A | 2 | a0004c0004t0001g0114a0004c0004t0001g0184 | 2 | HG02965.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1027-600C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279664 | ||||||
chr4:76279720
|
C | A | 1 | a0002c0002t0001g0058 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1027-544C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279720 | ||||||
chr4:76279722
|
A | G | 72 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(69): Show | 134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1027-542A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279722 | ||||||
chr4:76279913
|
A | T | 136 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(133): Show | 237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1027-351A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279913 | ||||||
chr4:76279927
|
T | A | 27 | a0003c0003t0001g0009a0003c0003t0001g0016a0003c0003t0001g0025others(24): Show | 48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1027-337T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76279927 | ||||||
chr4:76280065
|
G | C | 2 | a0002c0002t0001g0075a0002c0002t0001g0076 | 2 | HG01106.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1027-199G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76280065 | ||||||
chr4:76280179
|
G | A | 174 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 322 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.1027-85G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 6/7 | chr4 | 76280179 | ||||||
chr4:76280402
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1104+61C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280402 | ||||||
chr4:76280475
|
A | T | 1 | a0002c0002t0001g0117 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1104+134A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280475 | ||||||
chr4:76280485
|
C | T | 1 | a0003c0003t0001g0048 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1104+144C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280485 | ||||||
chr4:76280497
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1104+156C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280497 | ||||||
chr4:76280684
|
C | G | 2 | a0004c0004t0001g0114a0004c0004t0001g0184 | 2 | HG02965.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1104+343C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280684 | ||||||
chr4:76280710
|
G | A | 6 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1104+369G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280710 | ||||||
chr4:76280866
|
T | C | 22 | a0003c0003t0002g0100a0004c0004t0001g0008a0004c0004t0001g0014others(19): Show | 34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1104+525T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76280866 | ||||||
chr4:76281033
|
G | A | 1 | a0004c0004t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1104+692G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281033 | ||||||
chr4:76281251
|
A | T | 129 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0001g0001others(126): Show | 226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1104+910A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281251 | ||||||
chr4:76281322
|
C | G | 1 | a0004c0004t0001g0122 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1104+981C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281322 | ||||||
chr4:76281560
|
A | G | 136 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0182others(133): Show | 237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1104+1219A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281560 | ||||||
chr4:76281609
|
A | G | 137 | a0001c0001t0001g0105a0001c0001t0001g0177a0001c0001t0001g0178others(134): Show | 238 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1104+1268A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281609 | ||||||
chr4:76281659
|
A | G | 76 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(73): Show | 146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1104+1318A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281659 | ||||||
chr4:76281708
|
A | G | 114 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0001g0001others(111): Show | 203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1104+1367A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281708 | ||||||
chr4:76281729
|
C | A | 76 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(73): Show | 146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1104+1388C>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281729 | ||||||
chr4:76281765
|
G | A | 6 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(3): Show | 8 | HG02486.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1104+1424G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281765 | ||||||
chr4:76281821
|
C | T | 1 | a0002c0002t0001g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1104+1480C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281821 | ||||||
chr4:76281825
|
T | C | 1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1104+1484T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281825 | ||||||
chr4:76281888
|
G | A | 31 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0001g0019others(28): Show | 47 | HG00280.hp2 HG00597.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.1105-1493G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281888 | ||||||
chr4:76281890
|
C | T | 76 | a0002c0002t0001g0001a0002c0002t0001g0004a0002c0002t0001g0007others(73): Show | 146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1105-1491C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281890 | ||||||
chr4:76281961
|
G | A | 2 | a0001c0001t0001g0026a0003c0003t0001g0174 | 4 | HG02165.hp2 HG03195.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-1420G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281961 | ||||||
chr4:76281964
|
G | C | 28 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0001g0019others(25): Show | 44 | HG00280.hp2 HG00597.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.1105-1417G>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281964 | ||||||
chr4:76281994
|
G | A | 1 | a0003c0003t0001g0174 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1105-1387G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281994 | ||||||
chr4:76281999
|
A | G | 110 | a0001c0001t0001g0115a0001c0001t0001g0138a0001c0001t0001g0150others(107): Show | 196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1105-1382A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76281999 | ||||||
chr4:76282037
|
TAACATTT others(8): Show |
T | 1 | a0002c0002t0001g0059 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1105-1341_1105-132 others(19): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 76282037 | |||||
chr4:76282038
|
A | AACATTTG others(16): Show |
1 | a0002c0002t0001g0054 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1105-1319_1105-129 others(27): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 76282038 | |||||
chr4:76282038
|
AACATTTG others(16): Show |
A | 54 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0023others(51): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1105-1319_1105-129 others(27): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 76282038 | |||||
chr4:76282042
|
TTTGTATG others(11): Show |
T | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1105-1337_1105-132 others(22): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 76282042 | |||||
chr4:76282061
|
T | A | 1 | a0002c0002t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1105-1320T>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282061 | ||||||
chr4:76282062
|
ACATTTGT others(16): Show |
A | 3 | a0001c0001t0001g0157a0005c0005t0001g0104a0005c0005t0001g0168 | 3 | HG02486.hp2 HG03195.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1105-1318_1105-129 others(27): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282062 | ||||||
chr4:76282085
|
G | A | 5 | a0003c0003t0001g0032a0005c0005t0001g0038a0005c0005t0001g0052others(2): Show | 9 | HG02622.hp2 HG02723.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1105-1296G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282085 | ||||||
chr4:76282119
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0197 | 2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1105-1262G>A | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282119 | ||||||
chr4:76282123
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0197 | 2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1105-1258A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282123 | ||||||
chr4:76282124
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0197 | 2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1105-1257T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282124 | ||||||
chr4:76282260
|
C | G | 81 | a0001c0001t0001g0105a0001c0001t0001g0150a0002c0002t0001g0001others(78): Show | 151 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1105-1121C>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282260 | ||||||
chr4:76282458
|
T | C | 5 | a0005c0005t0001g0038a0005c0005t0001g0052a0005c0005t0001g0104others(2): Show | 7 | HG02486.hp2 HG02723.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-923T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282458 | ||||||
chr4:76282703
|
C | T | 1 | a0002c0002t0001g0013 | 4 | HG01884.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-678C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282703 | ||||||
chr4:76282706
|
CT | C | 74 | a0001c0001t0001g0105a0002c0002t0001g0001a0002c0002t0001g0004others(71): Show | 132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1105-674delT | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282706 | ||||||
chr4:76282919
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1105-462A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282919 | ||||||
chr4:76282963
|
A | T | 1 | a0003c0003t0001g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1105-418A>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76282963 | ||||||
chr4:76283152
|
T | C | 1 | a0002c0002t0001g0053 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1105-229T>C | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76283152 | ||||||
chr4:76283245
|
CAT | C | 18 | a0004c0004t0001g0008a0004c0004t0001g0014a0004c0004t0001g0024others(15): Show | 29 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1105-135_1105-134d others(4): Show |
FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76283245 | ||||||
chr4:76283347
|
C | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 280 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.1105-34C>T | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76283347 | ||||||
chr4:76283379
|
A | G | 1 | a0004c0004t0001g0184 | 1 | HG02965.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1105-2A>G | FAM47E | ENSG00000189157.14 | transcript | ENST00000424749.7 | protein_coding | 7/7 | chr4 | 76283379 |