geneid | 2147 |
---|---|
ensemblid | ENSG00000180210.15 |
hgncid | 3535 |
symbol | F2 |
name | coagulation factor II, thrombin |
refseq_nuc | NM_000506.5 |
refseq_prot | NP_000497.1 |
ensembl_nuc | ENST00000311907.10 |
ensembl_prot | ENSP00000308541.5 |
mane_status | MANE Select |
chr | chr11 |
start | 46719213 |
end | 46739506 |
strand | + |
ver | v1.2 |
region | chr11:46719213-46739506 |
region5000 | chr11:46714213-46744506 |
regionname0 | F2_chr11_46719213_46739506 |
regionname5000 | F2_chr11_46714213_46744506 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 622 | 266 | 93 | 47 | 83 | 11 | 31 | 65 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0002 | 0/1 | 622 | 82 | 1 | 14 | 60 | 1 | 5 | 50 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0003 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0004 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1869 | 227 | 72 | 38 | 80 | 10 | 26 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0002 | 0/1 | 1869 | 82 | 1 | 14 | 60 | 1 | 5 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0003 | 0/0 | 1869 | 20 | 19 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0004 | 0/0 | 1869 | 12 | 0 | 6 | 0 | 1 | 5 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0005 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0006 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0007 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0008 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0009 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0010 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0011 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
c0012 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 122 | 349 | 94 | 61 | 144 | 12 | 36 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
t0002 | 0/0 | 122 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 23 | 3 | 4 | 10 | 2 | 4 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0002 | 0/0 | 15 | 0 | 3 | 12 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0003 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0004 | 0/0 | 9 | 1 | 2 | 4 | 1 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0005 | 0/0 | 8 | 0 | 0 | 6 | 1 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0007 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0008 | 0/0 | 5 | 0 | 1 | 1 | 1 | 2 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0033 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0209 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1869 | 227 | 72 | 38 | 80 | 10 | 26 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0003 | 0/0 | 1869 | 20 | 19 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0004 | 0/0 | 1869 | 12 | 0 | 6 | 0 | 1 | 5 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0005 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0006 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0007 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0008 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0009 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0012 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0002c0002 | 0/1 | 1869 | 82 | 1 | 14 | 60 | 1 | 5 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0003c0011 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0004c0010 | 0/0 | 1869 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1990 | 227 | 72 | 38 | 80 | 10 | 26 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0003t0001 | 0/0 | 1990 | 20 | 19 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0004t0001 | 0/0 | 1990 | 11 | 0 | 5 | 0 | 1 | 5 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0004t0002 | 0/0 | 1990 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0005t0001 | 0/0 | 1990 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0006t0001 | 0/0 | 1990 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0007t0001 | 0/0 | 1990 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0008t0001 | 0/0 | 1990 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0009t0001 | 0/0 | 1990 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0001c0012t0001 | 0/0 | 1990 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0002c0002t0001 | 0/1 | 1990 | 82 | 1 | 14 | 60 | 1 | 5 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0003c0011t0001 | 0/0 | 1990 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
a0004c0010t0001 | 0/0 | 1990 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | copy fasta | chr11 | 46714213 | 46744506 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 23 | 3 | 4 | 10 | 2 | 4 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0003 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0004 | 0/0 | 8 | 1 | 2 | 3 | 1 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 6 | 1 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0007 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 1 | 1 | 2 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0033 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0005t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0006t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0007t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0008t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0009t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0001c0012t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0002 | 0/0 | 15 | 0 | 3 | 12 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0209 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0003c0011t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
a0004c0010t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0206 | EUR | FIN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00733 | hp1 | a0004 | c0010 | t0001 | g0018 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00735 | hp1 | a0001 | c0004 | t0001 | g0048 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01074 | hp1 | a0001 | c0004 | t0001 | g0050 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01109 | hp1 | a0001 | c0004 | t0002 | g0045 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0155 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01257 | hp2 | a0001 | c0004 | t0001 | g0052 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01261 | hp1 | a0001 | c0004 | t0001 | g0021 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01261 | hp2 | a0001 | c0008 | t0001 | g0024 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01433 | hp1 | a0001 | c0007 | t0001 | g0011 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01515 | hp1 | a0001 | c0004 | t0001 | g0049 | EUR | IBS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01981 | hp1 | a0001 | c0004 | t0001 | g0047 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02015 | hp1 | a0001 | c0009 | t0001 | g0160 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PEL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0156 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02896 | hp1 | a0001 | c0005 | t0001 | g0046 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0223 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03017 | hp2 | a0001 | c0004 | t0001 | g0051 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03098 | hp1 | a0001 | c0005 | t0001 | g0044 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0147 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0148 | AFR | ESN | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03688 | hp1 | a0001 | c0004 | t0001 | g0021 | SAS | STU | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0197 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03704 | hp2 | a0001 | c0004 | t0001 | g0054 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03710 | hp2 | a0001 | c0004 | t0001 | g0055 | SAS | PJL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0226 | SAS | BEB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0182 | SAS | BEB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG04115 | hp1 | a0001 | c0004 | t0001 | g0053 | SAS | STU | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | STU | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | CHB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18962 | hp1 | a0003 | c0011 | t0001 | g0188 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19011 | hp2 | a0001 | c0006 | t0001 | g0022 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19068 | hp1 | a0001 | c0012 | t0001 | g0004 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0149 | AFR | MSL | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | USA | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0209 | REF | REF | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0033 | REF | REF | F2_chr11_46714213_46744506 | F2 | chr11 | 46714213 | 46744506 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46720808
|
C | T | 1 | a0003 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.284C>T | p.Thr95Met | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/14 | 307/1990 | 284/1869 | 95/622 | chr11 | 46720808 | ||
chr11:46723453
|
C | T | 3 | a0002a0003a0004 | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
missense_variant | MODERATE | c.494C>T | p.Thr165Met | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/14 | 517/1990 | 494/1869 | 165/622 | chr11 | 46723453 | ||
chr11:46729406
|
G | A | 1 | a0004 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.1499G>A | p.Arg500Gln | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/14 | 1522/1990 | 1499/1869 | 500/622 | chr11 | 46729406 | ||
chr11:46739504
|
C | T | 1 | a0001 | 1 | HG01109.hp1 | splice_region_variant | LOW | c.*96C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 14/14 | chr11 | 46739504 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46720528
|
G | C | 1 | a0001c0006 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.246G>C | p.Val82Val | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 3/14 | 269/1990 | 246/1869 | 82/622 | chr11 | 46720528 | ||
chr11:46720543
|
C | T | 1 | a0001c0012 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.261C>T | p.Tyr87Tyr | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 3/14 | 284/1990 | 261/1869 | 87/622 | chr11 | 46720543 | ||
chr11:46723439
|
C | T | 1 | a0001c0003 | 20 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(17): Show |
synonymous_variant | LOW | c.480C>T | p.Pro160Pro | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/14 | 503/1990 | 480/1869 | 160/622 | chr11 | 46723439 | ||
chr11:46725896
|
C | T | 1 | a0001c0009 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.597C>T | p.Ser199Ser | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 7/14 | 620/1990 | 597/1869 | 199/622 | chr11 | 46725896 | ||
chr11:46726097
|
C | T | 1 | a0001c0008 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.798C>T | p.Asp266Asp | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 7/14 | 821/1990 | 798/1869 | 266/622 | chr11 | 46726097 | ||
chr11:46728098
|
G | A | 2 | a0001c0004a0001c0005 | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
synonymous_variant | LOW | c.1233G>A | p.Pro411Pro | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 10/14 | 1256/1990 | 1233/1869 | 411/622 | chr11 | 46728098 | ||
chr11:46729509
|
G | A | 1 | a0001c0007 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1602G>A | p.Pro534Pro | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/14 | 1625/1990 | 1602/1869 | 534/622 | chr11 | 46729509 | ||
chr11:46739396
|
G | A | 1 | a0001c0005 | 2 | HG02896.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.1857G>A | p.Gln619Gln | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 14/14 | 1880/1990 | 1857/1869 | 619/622 | chr11 | 46739396 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46719321
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0042 | 4 | HG02723.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.79+7G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 1/13 | chr11 | 46719321 | ||||||
chr11:46719470
|
G | T | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.79+156G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 1/13 | chr11 | 46719470 | ||||||
chr11:46719509
|
C | G | 1 | a0002c0002t0001g0231 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.80-193C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 1/13 | chr11 | 46719509 | ||||||
chr11:46719903
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.240+41G>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 2/13 | chr11 | 46719903 | ||||||
chr11:46719945
|
C | T | 59 | a0001c0001t0001g0040a0001c0001t0001g0228a0001c0001t0001g0229others(56): Show | 82 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.240+83C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 2/13 | chr11 | 46719945 | ||||||
chr11:46720066
|
C | T | 1 | a0002c0002t0001g0230 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.240+204C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 2/13 | chr11 | 46720066 | ||||||
chr11:46720358
|
C | A | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.241-165C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 2/13 | chr11 | 46720358 | ||||||
chr11:46720431
|
G | A | 2 | a0002c0002t0001g0017a0002c0002t0001g0182 | 4 | HG01070.hp2 HG01071.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-92G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 2/13 | chr11 | 46720431 | ||||||
chr11:46720497
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.241-26C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 2/13 | chr11 | 46720497 | ||||||
chr11:46720699
|
T | C | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.266-91T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 3/13 | chr11 | 46720699 | ||||||
chr11:46720876
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 55 | HG01070.hp1 HG01081.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.316+36G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46720876 | ||||||
chr11:46720938
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG00609.hp1 HG02040.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+98C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46720938 | ||||||
chr11:46720939
|
A | G | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.316+99A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46720939 | ||||||
chr11:46720973
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.316+133G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46720973 | ||||||
chr11:46721104
|
G | A | 1 | a0001c0001t0001g0026 | 2 | NA18964.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.316+264G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721104 | ||||||
chr11:46721186
|
G | A | 2 | a0002c0002t0001g0017a0002c0002t0001g0182 | 4 | HG01070.hp2 HG01071.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+346G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721186 | ||||||
chr11:46721193
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.316+353G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721193 | ||||||
chr11:46721218
|
A | ATTTTTAG others(793): Show |
1 | a0002c0002t0001g0186 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.316+856_316+857ins others(800): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721218 | |||||
chr11:46721218
|
A | ATTTTTAG others(794): Show |
46 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(43): Show | 69 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.316+856_316+857ins others(801): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721218 | |||||
chr11:46721218
|
A | ATTTTTAG others(795): Show |
4 | a0002c0002t0001g0088a0002c0002t0001g0225a0002c0002t0001g0226others(1): Show | 4 | HG03831.hp1 NA18961.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+856_316+857ins others(802): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721218 | |||||
chr11:46721294
|
G | GGCCTCAA others(794): Show |
1 | a0002c0002t0001g0189 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.316+856_316+857ins others(801): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721294 | |||||
chr11:46721338
|
C | G | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+498C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721338 | ||||||
chr11:46721341
|
T | A | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+501T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721341 | ||||||
chr11:46721343
|
A | G | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+503A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721343 | ||||||
chr11:46721348
|
A | T | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+508A>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721348 | ||||||
chr11:46721350
|
G | GTGGACGA others(21): Show |
1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+511_316+512ins others(28): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721350 | |||||
chr11:46721355
|
A | C | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+515A>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721355 | ||||||
chr11:46721361
|
C | G | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+521C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721361 | ||||||
chr11:46721362
|
A | T | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+522A>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721362 | ||||||
chr11:46721377
|
A | T | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+537A>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721377 | ||||||
chr11:46721380
|
C | T | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+540C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721380 | ||||||
chr11:46721381
|
G | T | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+541G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721381 | ||||||
chr11:46721382
|
A | T | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+542A>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721382 | ||||||
chr11:46721383
|
G | C | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+543G>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721383 | ||||||
chr11:46721386
|
T | G | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+546T>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721386 | ||||||
chr11:46721389
|
G | A | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+549G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721389 | ||||||
chr11:46721390
|
C | G | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+550C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721390 | ||||||
chr11:46721391
|
C | T | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+551C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721391 | ||||||
chr11:46721393
|
C | T | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+553C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721393 | ||||||
chr11:46721407
|
C | T | 1 | a0001c0004t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.316+567C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721407 | ||||||
chr11:46721468
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.316+628A>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721468 | ||||||
chr11:46721493
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0228 | 3 | HG02615.hp2 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.316+653A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721493 | ||||||
chr11:46721547
|
A | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | NA18973.hp1 NA19005.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+707A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721547 | ||||||
chr11:46721585
|
T | C | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.316+745T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721585 | ||||||
chr11:46721682
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0084others(21): Show | 33 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.316+842C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721682 | ||||||
chr11:46721697
|
T | C | 61 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(58): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.316+857T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721697 | ||||||
chr11:46721784
|
T | C | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.316+944T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721784 | ||||||
chr11:46721789
|
C | A | 1 | a0001c0001t0001g0089 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.316+949C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721789 | ||||||
chr11:46721805
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.316+965T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721805 | ||||||
chr11:46721807
|
A | C | 1 | a0001c0001t0001g0089 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.316+967A>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721807 | ||||||
chr11:46721841
|
A | AT | 12 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0081others(9): Show | 17 | HG01070.hp1 HG01081.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.316+1020dupT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721841 | |||||
chr11:46721841
|
A | ATT | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.316+1019_316+1020d others(4): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721841 | |||||
chr11:46721841
|
A | ATTTTTTT others(793): Show |
1 | a0002c0002t0001g0183 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.316+1019_316+1020i others(802): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721841 | |||||
chr11:46721841
|
A | ATTTTTTT others(795): Show |
1 | a0002c0002t0001g0230 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.317-1118_317-1117i others(804): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721841 | |||||
chr11:46721841
|
AT | A | 7 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG02280.hp2 HG02818.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.316+1020delT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721841 | |||||
chr11:46721842
|
T | TTTTTTTT others(792): Show |
1 | a0002c0002t0001g0185 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.316+1019_316+1020i others(801): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721842 | |||||
chr11:46721842
|
T | TTTTTTTT others(793): Show |
2 | a0002c0002t0001g0190a0002c0002t0001g0191 | 2 | NA18954.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.317-1118_317-1117i others(802): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 46721842 | |||||
chr11:46721882
|
G | A | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.316+1042G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721882 | ||||||
chr11:46721891
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.316+1051G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721891 | ||||||
chr11:46721912
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0097 | 3 | HG02486.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.316+1072G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46721912 | ||||||
chr11:46722313
|
C | G | 1 | a0001c0001t0001g0089 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.317-867C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722313 | ||||||
chr11:46722314
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.317-866G>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722314 | ||||||
chr11:46722334
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.317-846G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722334 | ||||||
chr11:46722647
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.317-533G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722647 | ||||||
chr11:46722807
|
G | A | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.317-373G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722807 | ||||||
chr11:46722818
|
T | C | 81 | a0001c0001t0001g0040a0001c0001t0001g0091a0001c0001t0001g0092others(78): Show | 106 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.317-362T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722818 | ||||||
chr11:46722819
|
G | A | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.317-361G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722819 | ||||||
chr11:46722920
|
G | A | 61 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(58): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.317-260G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722920 | ||||||
chr11:46722978
|
T | C | 76 | a0001c0001t0001g0040a0001c0001t0001g0228a0001c0004t0001g0021others(73): Show | 101 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.317-202T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722978 | ||||||
chr11:46722995
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317-185G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 4/13 | chr11 | 46722995 | ||||||
chr11:46723375
|
G | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
splice_region_variant&intron_variant | LOW | c.423-7G>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 5/13 | chr11 | 46723375 | ||||||
chr11:46723538
|
G | T | 1 | a0001c0001t0001g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.559+20G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46723538 | ||||||
chr11:46723759
|
G | A | 1 | a0002c0002t0001g0192 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.559+241G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46723759 | ||||||
chr11:46723767
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.559+249G>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46723767 | ||||||
chr11:46723771
|
T | A | 1 | a0001c0001t0001g0089 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.559+253T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46723771 | ||||||
chr11:46723772
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.559+254C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46723772 | ||||||
chr11:46723894
|
G | GA | 15 | a0001c0001t0001g0099a0001c0004t0001g0021a0001c0004t0001g0047others(12): Show | 16 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.559+386dupA | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 46723894 | |||||
chr11:46723901
|
AAAAGATG others(4): Show |
A | 1 | a0001c0001t0001g0089 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.559+384_559+394del others(11): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46723901 | ||||||
chr11:46723906
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.559+388A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46723906 | ||||||
chr11:46723930
|
G | A | 1 | a0002c0002t0001g0194 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.559+412G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46723930 | ||||||
chr11:46723995
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.559+477G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46723995 | ||||||
chr11:46724000
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.559+482G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724000 | ||||||
chr11:46724132
|
C | T | 15 | a0001c0001t0001g0056a0001c0003t0001g0006a0001c0003t0001g0035others(12): Show | 21 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.559+614C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724132 | ||||||
chr11:46724311
|
C | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0022others(14): Show | 30 | HG01070.hp1 HG01081.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.559+793C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724311 | ||||||
chr11:46724311
|
C | G | 1 | a0001c0003t0001g0152 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.559+793C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724311 | ||||||
chr11:46724460
|
C | T | 1 | a0002c0002t0001g0223 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.559+942C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724460 | ||||||
chr11:46724708
|
G | C | 61 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(58): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.560-1151G>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724708 | ||||||
chr11:46724746
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.560-1113T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724746 | ||||||
chr11:46724767
|
C | CT | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.560-1080dupT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 46724767 | |||||
chr11:46724773
|
T | G | 1 | a0002c0002t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.560-1086T>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724773 | ||||||
chr11:46724856
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.560-1003C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724856 | ||||||
chr11:46724930
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.560-929C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46724930 | ||||||
chr11:46725066
|
G | A | 61 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(58): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.560-793G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46725066 | ||||||
chr11:46725069
|
C | CT | 36 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(33): Show | 46 | HG01109.hp1 HG01109.hp2 HG01261.hp2 others(43): Show |
intron_variant | MODIFIER | c.560-772dupT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 46725069 | |||||
chr11:46725069
|
C | CTT | 36 | a0001c0001t0001g0040a0001c0001t0001g0056a0001c0001t0001g0077others(33): Show | 44 | HG00735.hp1 HG01074.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.560-773_560-772dup others(2): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 46725069 | |||||
chr11:46725069
|
C | CTTT | 56 | a0001c0003t0001g0151a0002c0002t0001g0002a0002c0002t0001g0017others(53): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.560-774_560-772dup others(3): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 46725069 | |||||
chr11:46725069
|
C | CTTTT | 6 | a0001c0001t0001g0140a0002c0002t0001g0219a0002c0002t0001g0220others(3): Show | 6 | HG02965.hp1 NA18977.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-775_560-772dup others(4): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 46725069 | |||||
chr11:46725104
|
CTG | C | 61 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(58): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.560-753_560-752del others(2): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 46725104 | |||||
chr11:46725515
|
C | G | 61 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(58): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.560-344C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46725515 | ||||||
chr11:46725640
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.560-219C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46725640 | ||||||
chr11:46725819
|
T | C | 4 | a0001c0001t0001g0232a0001c0004t0002g0045a0001c0005t0001g0044others(1): Show | 4 | HG01109.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.560-40T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 6/13 | chr11 | 46725819 | ||||||
chr11:46726237
|
G | A | 1 | a0002c0002t0001g0196 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.874+64G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 7/13 | chr11 | 46726237 | ||||||
chr11:46726303
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.874+130G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 7/13 | chr11 | 46726303 | ||||||
chr11:46726317
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.874+144G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 7/13 | chr11 | 46726317 | ||||||
chr11:46726429
|
T | C | 61 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(58): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.875-69T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 7/13 | chr11 | 46726429 | ||||||
chr11:46726479
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.875-19G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 7/13 | chr11 | 46726479 | ||||||
chr11:46726644
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1003+18C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 8/13 | chr11 | 46726644 | ||||||
chr11:46726647
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1003+21G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 8/13 | chr11 | 46726647 | ||||||
chr11:46726686
|
C | T | 1 | a0001c0004t0001g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1004-25C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 8/13 | chr11 | 46726686 | ||||||
chr11:46726900
|
C | A | 1 | a0002c0002t0001g0197 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1130+63C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 9/13 | chr11 | 46726900 | ||||||
chr11:46727094
|
T | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1130+257T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 9/13 | chr11 | 46727094 | ||||||
chr11:46727579
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0228 | 3 | HG02615.hp2 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1131-417G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 9/13 | chr11 | 46727579 | ||||||
chr11:46727684
|
G | A | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1131-312G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 9/13 | chr11 | 46727684 | ||||||
chr11:46727692
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19077.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1131-304C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 9/13 | chr11 | 46727692 | ||||||
chr11:46727696
|
T | C | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1131-300T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 9/13 | chr11 | 46727696 | ||||||
chr11:46727784
|
T | A | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1131-212T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 9/13 | chr11 | 46727784 | ||||||
chr11:46727833
|
C | T | 1 | a0002c0002t0001g0218 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1131-163C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 9/13 | chr11 | 46727833 | ||||||
chr11:46728274
|
A | G | 1 | a0001c0003t0001g0150 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1298+111A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 10/13 | chr11 | 46728274 | ||||||
chr11:46728514
|
C | G | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1299-150C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 10/13 | chr11 | 46728514 | ||||||
chr11:46728975
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG00099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1472+138G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 11/13 | chr11 | 46728975 | ||||||
chr11:46728983
|
GT | G | 24 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0024others(21): Show | 29 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1472+150delT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 46728983 | |||||
chr11:46728991
|
T | A | 4 | a0002c0002t0001g0186a0002c0002t0001g0190a0002c0002t0001g0198others(1): Show | 4 | NA18948.hp1 NA19002.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472+154T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 11/13 | chr11 | 46728991 | ||||||
chr11:46729088
|
T | C | 139 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(136): Show | 191 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.1472+251T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 11/13 | chr11 | 46729088 | ||||||
chr11:46729268
|
C | A | 1 | a0001c0009t0001g0160 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1473-112C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 11/13 | chr11 | 46729268 | ||||||
chr11:46729269
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0022others(28): Show | 50 | HG01070.hp1 HG01081.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.1473-111T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 11/13 | chr11 | 46729269 | ||||||
chr11:46729296
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1473-84A>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 11/13 | chr11 | 46729296 | ||||||
chr11:46729611
|
G | T | 2 | a0002c0002t0001g0196a0002c0002t0001g0222 | 2 | NA19007.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1654+50G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46729611 | ||||||
chr11:46729634
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1654+73A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46729634 | ||||||
chr11:46729851
|
T | C | 61 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(58): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1654+290T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46729851 | ||||||
chr11:46729945
|
T | TAGG | 54 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(51): Show | 78 | HG00735.hp1 HG01070.hp1 HG01074.hp1 others(75): Show |
intron_variant | MODIFIER | c.1654+388_1654+390d others(5): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46729945 | |||||
chr11:46729960
|
A | G | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1654+399A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46729960 | ||||||
chr11:46729984
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1654+423C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46729984 | ||||||
chr11:46730017
|
G | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0024others(21): Show | 29 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1654+456G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46730017 | ||||||
chr11:46730205
|
CAGG | C | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1654+647_1654+649d others(5): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46730205 | |||||
chr11:46730232
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1654+671G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46730232 | ||||||
chr11:46730298
|
T | G | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1654+737T>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46730298 | ||||||
chr11:46730796
|
A | ATATATAT others(39): Show |
1 | a0001c0005t0001g0044 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1654+1238_1654+123 others(50): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46730796 | |||||
chr11:46730796
|
A | ATATATAT others(37): Show |
4 | a0001c0004t0001g0047a0001c0004t0001g0048a0001c0004t0001g0049others(1): Show | 4 | HG00735.hp1 HG01515.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654+1238_1654+123 others(48): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46730796 | |||||
chr11:46730796
|
A | ATATATAT others(35): Show |
1 | a0001c0004t0001g0050 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1654+1238_1654+123 others(46): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46730796 | |||||
chr11:46730796
|
A | ATATATAT others(33): Show |
2 | a0001c0004t0001g0051a0001c0004t0001g0054 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1654+1238_1654+123 others(44): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46730796 | |||||
chr11:46730796
|
A | ATATATAT others(31): Show |
3 | a0001c0004t0001g0021a0001c0004t0001g0052a0001c0004t0002g0045 | 4 | HG01109.hp1 HG01257.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654+1238_1654+123 others(42): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46730796 | |||||
chr11:46730796
|
A | ATATATAT others(25): Show |
2 | a0001c0004t0001g0053a0001c0005t0001g0046 | 2 | HG02896.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1654+1238_1654+123 others(36): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46730796 | |||||
chr11:46730813
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1654+1252G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46730813 | ||||||
chr11:46730862
|
C | CA | 103 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(100): Show | 141 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1654+1315dupA | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46730862 | |||||
chr11:46730862
|
C | CAA | 19 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0077others(16): Show | 20 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1654+1314_1654+131 others(6): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46730862 | |||||
chr11:46730986
|
G | C | 1 | a0001c0001t0001g0029 | 2 | HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1654+1425G>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46730986 | ||||||
chr11:46731095
|
G | T | 1 | a0001c0001t0001g0129 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1654+1534G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731095 | ||||||
chr11:46731109
|
G | T | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1654+1548G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731109 | ||||||
chr11:46731282
|
G | A | 20 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0024others(17): Show | 25 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1654+1721G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731282 | ||||||
chr11:46731408
|
T | C | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1654+1847T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731408 | ||||||
chr11:46731570
|
A | AG | 8 | a0001c0004t0001g0021a0001c0004t0001g0048a0001c0004t0001g0049others(5): Show | 9 | HG00735.hp1 HG01074.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1654+2012dupG | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46731570 | |||||
chr11:46731573
|
G | GA | 52 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0043others(49): Show | 66 | HG00099.hp1 HG00609.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1654+2028dupA | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46731573 | |||||
chr11:46731573
|
G | GGA | 5 | a0001c0004t0001g0047a0001c0004t0001g0053a0001c0004t0002g0045others(2): Show | 5 | HG01109.hp1 HG01981.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654+2012_1654+201 others(6): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731573 | ||||||
chr11:46731573
|
GA | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0024others(24): Show | 34 | HG00099.hp2 HG01261.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.1654+2028delA | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46731573 | |||||
chr11:46731574
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1654+2013A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731574 | ||||||
chr11:46731695
|
C | T | 1 | a0001c0009t0001g0160 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1654+2134C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731695 | ||||||
chr11:46731912
|
G | GT | 15 | a0001c0001t0001g0076a0001c0001t0001g0115a0002c0002t0001g0019others(12): Show | 18 | HG00621.hp2 HG00673.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1654+2373dupT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46731912 | |||||
chr11:46731912
|
G | GTTTTTTT others(13): Show |
1 | a0001c0001t0001g0228 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1654+2354_1654+237 others(24): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46731912 | |||||
chr11:46731912
|
G | GTTTTTTT others(14): Show |
1 | a0001c0001t0001g0040 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1654+2353_1654+237 others(25): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46731912 | |||||
chr11:46731912
|
GT | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1654+2373delT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46731912 | |||||
chr11:46731912
|
GTTTTTT | G | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1654+2368_1654+237 others(10): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46731912 | |||||
chr11:46731918
|
T | TG | 6 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 6 | HG01496.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1654+2357_1654+235 others(5): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731918 | ||||||
chr11:46731919
|
T | G | 25 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0022others(22): Show | 44 | HG01070.hp1 HG01081.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.1654+2358T>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731919 | ||||||
chr11:46731924
|
T | G | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1654+2363T>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731924 | ||||||
chr11:46731978
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1654+2417C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46731978 | ||||||
chr11:46732143
|
T | C | 15 | a0001c0001t0001g0080a0001c0003t0001g0006a0001c0003t0001g0035others(12): Show | 21 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1654+2582T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46732143 | ||||||
chr11:46732174
|
A | G | 2 | a0002c0002t0001g0198a0002c0002t0001g0199 | 2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1654+2613A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46732174 | ||||||
chr11:46732202
|
A | G | 3 | a0002c0002t0001g0018a0002c0002t0001g0214a0004c0010t0001g0018 | 4 | HG00733.hp1 HG01074.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1654+2641A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46732202 | ||||||
chr11:46732345
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1654+2784C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46732345 | ||||||
chr11:46732458
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1654+2897C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46732458 | ||||||
chr11:46732691
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1654+3130G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46732691 | ||||||
chr11:46732976
|
C | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0141others(1): Show | 7 | HG02559.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654+3415C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46732976 | ||||||
chr11:46733099
|
C | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0024others(21): Show | 29 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1654+3538C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46733099 | ||||||
chr11:46733507
|
C | T | 1 | a0002c0002t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1654+3946C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46733507 | ||||||
chr11:46733621
|
A | T | 1 | a0002c0002t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1654+4060A>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46733621 | ||||||
chr11:46733682
|
T | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1654+4121T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46733682 | ||||||
chr11:46733710
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1654+4149T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46733710 | ||||||
chr11:46733729
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1654+4168G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46733729 | ||||||
chr11:46733782
|
C | CT | 92 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(89): Show | 118 | HG00609.hp2 HG00621.hp1 HG00642.hp2 others(115): Show |
intron_variant | MODIFIER | c.1654+4245dupT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46733782 | |||||
chr11:46733782
|
C | CTT | 18 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 21 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.1654+4244_1654+424 others(6): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46733782 | |||||
chr11:46733782
|
CT | C | 7 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0118others(4): Show | 8 | HG00741.hp1 HG01109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1654+4245delT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46733782 | |||||
chr11:46733782
|
CTT | C | 10 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(7): Show | 11 | HG00735.hp1 HG01074.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1654+4244_1654+424 others(6): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46733782 | |||||
chr11:46733782
|
CTTTTTTT others(1): Show |
C | 4 | a0002c0002t0001g0017a0002c0002t0001g0182a0002c0002t0001g0206others(1): Show | 6 | HG00280.hp2 HG00741.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1654+4238_1654+424 others(12): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46733782 | |||||
chr11:46733838
|
G | C | 10 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(7): Show | 11 | HG00735.hp1 HG01074.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1654+4277G>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46733838 | ||||||
chr11:46733891
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0109others(1): Show | 7 | HG01255.hp2 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1654+4330C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46733891 | ||||||
chr11:46733914
|
A | G | 12 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(9): Show | 13 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1654+4353A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46733914 | ||||||
chr11:46734103
|
T | A | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1654+4542T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46734103 | ||||||
chr11:46734105
|
AT | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0119a0001c0001t0001g0125 | 6 | HG00733.hp2 HG00735.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1654+4554delT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46734105 | |||||
chr11:46734244
|
C | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0022others(31): Show | 53 | HG01070.hp1 HG01081.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.1654+4683C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46734244 | ||||||
chr11:46734534
|
A | G | 1 | a0002c0002t0001g0223 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1655-4514A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46734534 | ||||||
chr11:46734538
|
G | T | 1 | a0001c0001t0001g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1655-4510G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46734538 | ||||||
chr11:46734679
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0169 | 4 | NA18941.hp2 NA18970.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1655-4369C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46734679 | ||||||
chr11:46734947
|
T | A | 1 | a0002c0002t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1655-4101T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46734947 | ||||||
chr11:46734958
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-4090T>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46734958 | ||||||
chr11:46734959
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-4089G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46734959 | ||||||
chr11:46734988
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-4060C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46734988 | ||||||
chr11:46735003
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-4045C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735003 | ||||||
chr11:46735004
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-4044T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735004 | ||||||
chr11:46735015
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-4033C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735015 | ||||||
chr11:46735127
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-3921C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735127 | ||||||
chr11:46735128
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-3920A>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735128 | ||||||
chr11:46735267
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-3781C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735267 | ||||||
chr11:46735268
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-3780T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735268 | ||||||
chr11:46735269
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-3779C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735269 | ||||||
chr11:46735340
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-3708C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735340 | ||||||
chr11:46735380
|
G | T | 1 | a0002c0002t0001g0231 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1655-3668G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735380 | ||||||
chr11:46735467
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1655-3581T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735467 | ||||||
chr11:46735533
|
GGATTGCT others(3): Show |
G | 1 | a0002c0002t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1655-3513_1655-350 others(14): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46735533 | |||||
chr11:46735641
|
G | A | 11 | a0001c0001t0001g0080a0001c0003t0001g0006a0001c0003t0001g0035others(8): Show | 17 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1655-3407G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735641 | ||||||
chr11:46735651
|
G | A | 5 | a0002c0002t0001g0038a0002c0002t0001g0184a0002c0002t0001g0207others(2): Show | 6 | NA18949.hp2 NA18957.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.1655-3397G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735651 | ||||||
chr11:46735654
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1655-3394G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735654 | ||||||
chr11:46735656
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0111 | 2 | HG00099.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1655-3392C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735656 | ||||||
chr11:46735748
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-3300C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735748 | ||||||
chr11:46735769
|
A | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1655-3279A>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735769 | ||||||
chr11:46735796
|
T | C | 2 | a0002c0002t0001g0198a0002c0002t0001g0199 | 2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1655-3252T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735796 | ||||||
chr11:46735973
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1655-3075G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46735973 | ||||||
chr11:46736068
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-2980T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736068 | ||||||
chr11:46736219
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-2829C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736219 | ||||||
chr11:46736252
|
A | ACCTTTAT | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1655-2794_1655-278 others(11): Show |
F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46736252 | |||||
chr11:46736290
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1655-2758A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736290 | ||||||
chr11:46736314
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1655-2734T>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736314 | ||||||
chr11:46736486
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1655-2562C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736486 | ||||||
chr11:46736487
|
G | A | 12 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(9): Show | 13 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1655-2561G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736487 | ||||||
chr11:46736557
|
C | G | 1 | a0002c0002t0001g0205 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1655-2491C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736557 | ||||||
chr11:46736616
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0042 | 4 | HG02723.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1655-2432T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736616 | ||||||
chr11:46736728
|
G | A | 2 | a0001c0003t0001g0035a0001c0003t0001g0155 | 3 | HG01243.hp1 HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1655-2320G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736728 | ||||||
chr11:46736736
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1655-2312C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736736 | ||||||
chr11:46736740
|
G | A | 61 | a0002c0002t0001g0002a0002c0002t0001g0017a0002c0002t0001g0018others(58): Show | 84 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1655-2308G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736740 | ||||||
chr11:46736833
|
C | T | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1655-2215C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736833 | ||||||
chr11:46736905
|
G | C | 1 | a0001c0001t0001g0090 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1655-2143G>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736905 | ||||||
chr11:46736921
|
T | C | 2 | a0002c0002t0001g0183a0002c0002t0001g0194 | 2 | NA18960.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1655-2127T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736921 | ||||||
chr11:46736950
|
G | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0141others(1): Show | 7 | HG02559.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1655-2098G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46736950 | ||||||
chr11:46737035
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0090a0001c0001t0001g0228 | 4 | HG02280.hp1 HG02615.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1655-2013T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737035 | ||||||
chr11:46737065
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-1983T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737065 | ||||||
chr11:46737074
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-1974T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737074 | ||||||
chr11:46737075
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-1973A>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737075 | ||||||
chr11:46737103
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-1945C>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737103 | ||||||
chr11:46737109
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-1939T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737109 | ||||||
chr11:46737110
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-1938C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737110 | ||||||
chr11:46737111
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-1937T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737111 | ||||||
chr11:46737124
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1655-1924T>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737124 | ||||||
chr11:46737316
|
A | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0141others(1): Show | 7 | HG02559.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1655-1732A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737316 | ||||||
chr11:46737332
|
C | T | 13 | a0001c0004t0001g0021a0001c0004t0001g0047a0001c0004t0001g0048others(10): Show | 14 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1655-1716C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737332 | ||||||
chr11:46737441
|
C | CT | 41 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0020others(38): Show | 53 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(50): Show |
intron_variant | MODIFIER | c.1655-1590dupT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46737441 | |||||
chr11:46737441
|
CT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1655-1590delT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46737441 | |||||
chr11:46737483
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1655-1565C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737483 | ||||||
chr11:46737534
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0078 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1655-1514G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737534 | ||||||
chr11:46737565
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | NA18973.hp1 NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1655-1483C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737565 | ||||||
chr11:46737646
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1655-1402G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737646 | ||||||
chr11:46737704
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1655-1344C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737704 | ||||||
chr11:46737734
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1655-1314G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737734 | ||||||
chr11:46737755
|
A | G | 1 | a0002c0002t0001g0189 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1655-1293A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737755 | ||||||
chr11:46737839
|
C | CT | 26 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0020others(23): Show | 32 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1655-1197dupT | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 46737839 | |||||
chr11:46737851
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1655-1197T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737851 | ||||||
chr11:46737963
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1655-1085C>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737963 | ||||||
chr11:46737964
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1655-1084G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46737964 | ||||||
chr11:46738021
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(120): Show | 172 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1655-1027A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738021 | ||||||
chr11:46738045
|
G | A | 2 | a0001c0003t0001g0149a0001c0003t0001g0150 | 2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1655-1003G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738045 | ||||||
chr11:46738084
|
A | G | 21 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0024others(18): Show | 26 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1655-964A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738084 | ||||||
chr11:46738159
|
T | C | 6 | a0002c0002t0001g0017a0002c0002t0001g0182a0002c0002t0001g0206others(3): Show | 8 | HG00280.hp2 HG00741.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1655-889T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738159 | ||||||
chr11:46738241
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0093others(1): Show | 7 | HG02559.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1655-807C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738241 | ||||||
chr11:46738259
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0097 | 3 | HG02486.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1655-789A>G | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738259 | ||||||
chr11:46738288
|
A | C | 1 | a0002c0002t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1655-760A>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738288 | ||||||
chr11:46738301
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1655-747G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738301 | ||||||
chr11:46738366
|
G | A | 3 | a0001c0001t0001g0072a0001c0005t0001g0044a0001c0005t0001g0046 | 3 | HG02717.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1655-682G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738366 | ||||||
chr11:46738570
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(74): Show | 126 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1655-478C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738570 | ||||||
chr11:46738612
|
T | C | 1 | a0002c0002t0001g0227 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1655-436T>C | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738612 | ||||||
chr11:46738712
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0065others(5): Show | 10 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1655-336C>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738712 | ||||||
chr11:46738916
|
G | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1655-132G>T | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 12/13 | chr11 | 46738916 | ||||||
chr11:46739206
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(38): Show | 78 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.1726-59G>A | F2 | ENSG00000180210.15 | transcript | ENST00000311907.10 | protein_coding | 13/13 | chr11 | 46739206 |