geneid | 619208 |
---|---|
ensemblid | ENSG00000203778.8 |
hgncid | 33858 |
symbol | FAM229B |
name | family with sequence similarity 229 member B |
refseq_nuc | NM_001033564.3 |
refseq_prot | NP_001028736.1 |
ensembl_nuc | ENST00000368656.7 |
ensembl_prot | ENSP00000357645.2 |
mane_status | MANE Select |
chr | chr6 |
start | 112087591 |
end | 112102790 |
strand | + |
ver | v1.2 |
region | chr6:112087591-112102790 |
region5000 | chr6:112082591-112107790 |
regionname0 | FAM229B_chr6_112087591_112102790 |
regionname5000 | FAM229B_chr6_112082591_112107790 |
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 | 1/1 | 80 | 405 | 86 | 69 | 193 | 13 | 42 | 148 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0002 | 0/0 | 80 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0003 | 0/0 | 80 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0004 | 0/0 | 80 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0005 | 0/0 | 80 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
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 | 1/1 | 243 | 405 | 86 | 69 | 193 | 13 | 42 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
c0002 | 0/0 | 243 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
c0003 | 0/0 | 243 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
c0004 | 0/0 | 243 | 3 | 3 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
c0005 | 0/0 | 243 | 2 | 0 | 1 | 0 | 1 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
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 | 2309 | 177 | 18 | 35 | 89 | 7 | 26 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0002 | 0/0 | 2310 | 99 | 14 | 14 | 59 | 3 | 9 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0003 | 0/0 | 2309 | 64 | 13 | 17 | 26 | 4 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0004 | 0/0 | 2309 | 36 | 17 | 2 | 14 | 0 | 3 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0005 | 0/0 | 2309 | 14 | 14 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0006 | 0/0 | 2310 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0007 | 0/0 | 2302 | 3 | 2 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0008 | 0/0 | 2309 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0009 | 0/0 | 2309 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0010 | 0/0 | 2309 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0011 | 0/0 | 2309 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0012 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0013 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0014 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0015 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0016 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0017 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0018 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0019 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0020 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0021 | 0/0 | 2309 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
t0022 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
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 | 1/1 | 65 | 3 | 17 | 31 | 2 | 10 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0002 | 0/0 | 40 | 10 | 9 | 14 | 3 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0003 | 0/0 | 33 | 0 | 0 | 29 | 0 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0004 | 0/0 | 30 | 7 | 5 | 13 | 2 | 3 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0005 | 0/0 | 22 | 0 | 5 | 11 | 2 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0006 | 0/0 | 18 | 0 | 4 | 10 | 1 | 3 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0007 | 0/0 | 16 | 9 | 0 | 7 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0008 | 0/0 | 12 | 4 | 2 | 6 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0009 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0010 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0013 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0014 | 0/0 | 6 | 2 | 1 | 2 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0015 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0016 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0018 | 0/0 | 5 | 3 | 0 | 1 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0019 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0020 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0021 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
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 | 1/1 | 243 | 405 | 86 | 69 | 193 | 13 | 42 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0002c0002 | 0/0 | 243 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0003c0003 | 0/0 | 243 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0004c0004 | 0/0 | 243 | 3 | 3 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0005c0005 | 0/0 | 243 | 2 | 0 | 1 | 0 | 1 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2551 | 169 | 13 | 34 | 88 | 6 | 26 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0002 | 0/0 | 2552 | 99 | 14 | 14 | 59 | 3 | 9 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0003 | 0/0 | 2551 | 62 | 13 | 17 | 24 | 4 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0004 | 0/0 | 2551 | 36 | 17 | 2 | 14 | 0 | 3 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0005 | 0/0 | 2551 | 14 | 14 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0006 | 0/0 | 2552 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0007 | 0/0 | 2544 | 3 | 2 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0008 | 0/0 | 2551 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0009 | 0/0 | 2551 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0010 | 0/0 | 2551 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0012 | 0/0 | 2552 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0013 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0014 | 0/0 | 2552 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0015 | 0/0 | 2552 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0017 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0018 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0019 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0020 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0021 | 0/0 | 2551 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0001c0001t0022 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0002c0002t0001 | 0/0 | 2551 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0003c0003t0001 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0003c0003t0003 | 0/0 | 2551 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0004c0004t0011 | 0/0 | 2551 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0004c0004t0016 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
a0005c0005t0001 | 0/0 | 2551 | 2 | 0 | 1 | 0 | 1 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | copy fasta | chr6 | 112082591 | 112107790 |
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 | 1/1 | 59 | 2 | 16 | 28 | 1 | 10 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0005 | 0/0 | 21 | 0 | 5 | 10 | 2 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0006 | 0/0 | 18 | 0 | 4 | 10 | 1 | 3 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0009 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0019 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0021 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0002 | 0/0 | 39 | 9 | 9 | 14 | 3 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0003 | 0/0 | 33 | 0 | 0 | 29 | 0 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0014 | 0/0 | 5 | 1 | 1 | 2 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0015 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0004 | 0/0 | 25 | 5 | 5 | 10 | 2 | 3 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0008 | 0/0 | 11 | 4 | 2 | 5 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0010 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0013 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0007 | 0/0 | 16 | 9 | 0 | 7 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0018 | 0/0 | 5 | 3 | 0 | 1 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0005g0016 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0005g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0005g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0006g0020 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0007g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0008g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0014g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0015g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0017g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0018g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0019g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0020g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0021g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0001c0001t0022g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0002c0002t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0002c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0003c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0003c0003t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0003c0003t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0004c0004t0011g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0004c0004t0016g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
a0005c0005t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0013 | EUR | GBR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00597 | hp2 | a0001 | c0001 | t0017 | g0005 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00609 | hp1 | a0001 | c0001 | t0008 | g0090 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0086 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02004 | hp1 | a0005 | c0005 | t0001 | g0001 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02004 | hp2 | a0001 | c0001 | t0021 | g0010 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02055 | hp2 | a0004 | c0004 | t0011 | g0027 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02074 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02155 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | CDX | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02280 | hp1 | a0001 | c0001 | t0022 | g0004 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0087 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02886 | hp1 | a0001 | c0001 | t0010 | g0056 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03195 | hp2 | a0001 | c0001 | t0019 | g0052 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03579 | hp2 | a0001 | c0001 | t0020 | g0004 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0067 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0075 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0054 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0018 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18747 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | CHB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18939 | hp1 | a0001 | c0001 | t0018 | g0039 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18948 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18991 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19056 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19076 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19076 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19085 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ASW | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ASW | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20752 | hp1 | a0005 | c0005 | t0001 | g0001 | EUR | TSI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0013 | EUR | TSI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02109 | hp1 | a0004 | c0004 | t0011 | g0027 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0048 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | USA | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | USA | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | USA | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA20300 | hp2 | a0004 | c0004 | t0016 | g0044 | AFR | USA | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:112099297
|
T | G | 1 | a0002 | 5 | HG01884.hp2 HG02486.hp2 HG03209.hp1 others(2): Show |
missense_variant | MODERATE | c.14T>G | p.Phe5Cys | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/4 | 319/2551 | 14/243 | 5/80 | chr6 | 112099297 | ||
chr6:112099312
|
G | A | 1 | a0005 | 2 | HG02004.hp1 NA20752.hp1 |
missense_variant | MODERATE | c.29G>A | p.Arg10Lys | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/4 | 334/2551 | 29/243 | 10/80 | chr6 | 112099312 | ||
chr6:112100722
|
G | A | 1 | a0003 | 3 | HG02155.hp2 NA18959.hp2 NA19076.hp1 |
missense_variant | MODERATE | c.178G>A | p.Val60Ile | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 483/2551 | 178/243 | 60/80 | chr6 | 112100722 | ||
chr6:112100731
|
T | A | 1 | a0004 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.187T>A | p.Tyr63Asn | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 492/2551 | 187/243 | 63/80 | chr6 | 112100731 |
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 |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:112097055
|
T | C | 1 | a0001c0001t0012 | 1 | HG03453.hp2 | 5_prime_UTR_variant | MODIFIER | c.-161T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/4 | 2229 | chr6 | 112097055 | |||||
chr6:112097086
|
G | A | 1 | a0001c0001t0004 | 36 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-130G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/4 | 2198 | chr6 | 112097086 | |||||
chr6:112099276
|
A | G | 1 | a0001c0001t0022 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-8A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/4 | 8 | chr6 | 112099276 | |||||
chr6:112100824
|
A | G | 1 | a0004c0004t0011 | 2 | HG02055.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*37A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 37 | chr6 | 112100824 | |||||
chr6:112100901
|
G | A | 1 | a0001c0001t0013 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 114 | chr6 | 112100901 | |||||
chr6:112100924
|
C | T | 1 | a0001c0001t0021 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 137 | chr6 | 112100924 | |||||
chr6:112100951
|
T | C | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(3): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*164T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 164 | chr6 | 112100951 | |||||
chr6:112100980
|
T | C | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 193 | chr6 | 112100980 | |||||
chr6:112101018
|
C | T | 1 | a0001c0001t0008 | 3 | HG00609.hp1 HG02074.hp1 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*231C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 231 | chr6 | 112101018 | |||||
chr6:112101159
|
TGCTACTT others(1): Show |
T | 1 | a0001c0001t0007 | 3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*377_*384delCTTGGC others(2): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 377 | INFO_REALIGN_3_PRIME | chr6 | 112101159 | ||||
chr6:112101187
|
G | T | 1 | a0001c0001t0020 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 400 | chr6 | 112101187 | |||||
chr6:112101206
|
T | A | 1 | a0001c0001t0009 | 2 | NA19056.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*419T>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 419 | chr6 | 112101206 | |||||
chr6:112101365
|
C | G | 1 | a0001c0001t0019 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 578 | chr6 | 112101365 | |||||
chr6:112101444
|
T | C | 10 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(7): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*657T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 657 | chr6 | 112101444 | |||||
chr6:112101461
|
A | C | 10 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(7): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*674A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 674 | chr6 | 112101461 | |||||
chr6:112101595
|
T | C | 1 | a0001c0001t0015 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 808 | chr6 | 112101595 | |||||
chr6:112101613
|
A | G | 1 | a0001c0001t0005 | 14 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*826A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 826 | chr6 | 112101613 | |||||
chr6:112101638
|
G | A | 1 | a0001c0001t0017 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*851G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 851 | chr6 | 112101638 | |||||
chr6:112101710
|
A | G | 1 | a0004c0004t0016 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*923A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 923 | chr6 | 112101710 | |||||
chr6:112101824
|
G | A | 1 | a0001c0001t0018 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1037G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1037 | chr6 | 112101824 | |||||
chr6:112102003
|
G | A | 4 | a0001c0001t0005a0001c0001t0019a0004c0004t0011others(1): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1216G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1216 | chr6 | 112102003 | |||||
chr6:112102059
|
G | C | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(3): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1272G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1272 | chr6 | 112102059 | |||||
chr6:112102079
|
T | C | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1292 | chr6 | 112102079 | |||||
chr6:112102195
|
C | T | 1 | a0004c0004t0016 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1408C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1408 | chr6 | 112102195 | |||||
chr6:112102281
|
C | T | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1494C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1494 | chr6 | 112102281 | |||||
chr6:112102312
|
C | T | 1 | a0001c0001t0010 | 2 | HG02886.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1525C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1525 | chr6 | 112102312 | |||||
chr6:112102379
|
G | C | 3 | a0001c0001t0002a0001c0001t0012a0001c0001t0015 | 101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1592G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1592 | chr6 | 112102379 | |||||
chr6:112102484
|
C | CA | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(3): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1706dupA | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1707 | INFO_REALIGN_3_PRIME | chr6 | 112102484 | ||||
chr6:112102607
|
A | G | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(15): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1820A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1820 | chr6 | 112102607 | |||||
chr6:112102640
|
G | A | 1 | a0001c0001t0010 | 2 | HG02886.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1853G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1853 | chr6 | 112102640 | |||||
chr6:112102741
|
C | A | 1 | a0001c0001t0006 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1954C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1954 | chr6 | 112102741 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:112087778
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-176+58A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112087778 | ||||||
chr6:112087805
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-176+85C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112087805 | ||||||
chr6:112087909
|
T | C | 2 | a0004c0004t0011g0027a0004c0004t0016g0044 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-176+189T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112087909 | ||||||
chr6:112087991
|
A | G | 2 | a0001c0001t0002g0043a0001c0001t0002g0092 | 3 | HG01891.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-176+271A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112087991 | ||||||
chr6:112088027
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-176+307G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088027 | ||||||
chr6:112088066
|
G | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0045others(3): Show | 13 | HG01433.hp1 HG02027.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-176+346G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088066 | ||||||
chr6:112088095
|
T | C | 1 | a0001c0001t0014g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-176+375T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088095 | ||||||
chr6:112088149
|
T | G | 2 | a0001c0001t0003g0049a0001c0001t0003g0050 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-176+429T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088149 | ||||||
chr6:112088269
|
T | G | 1 | a0001c0001t0004g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-176+549T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088269 | ||||||
chr6:112088421
|
T | C | 2 | a0004c0004t0011g0027a0004c0004t0016g0044 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-176+701T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088421 | ||||||
chr6:112088600
|
C | T | 1 | a0001c0001t0008g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-176+880C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088600 | ||||||
chr6:112088601
|
G | A | 3 | a0001c0001t0019g0052a0004c0004t0011g0027a0004c0004t0016g0044 | 4 | HG02055.hp2 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176+881G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088601 | ||||||
chr6:112088810
|
G | A | 1 | a0004c0004t0011g0027 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-176+1090G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088810 | ||||||
chr6:112088908
|
C | G | 1 | a0001c0001t0006g0020 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176+1188C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088908 | ||||||
chr6:112088922
|
G | T | 1 | a0001c0001t0003g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-176+1202G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088922 | ||||||
chr6:112088946
|
A | C | 1 | a0001c0001t0002g0089 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-176+1226A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088946 | ||||||
chr6:112089076
|
T | C | 1 | a0001c0001t0014g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-176+1356T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089076 | ||||||
chr6:112089133
|
A | G | 27 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(24): Show | 123 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-176+1413A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089133 | ||||||
chr6:112089283
|
A | G | 3 | a0001c0001t0019g0052a0004c0004t0011g0027a0004c0004t0016g0044 | 4 | HG02055.hp2 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176+1563A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089283 | ||||||
chr6:112089388
|
G | GA | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 115 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-176+1672dupA | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112089388 | |||||
chr6:112089529
|
A | G | 2 | a0004c0004t0011g0027a0004c0004t0016g0044 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-176+1809A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089529 | ||||||
chr6:112089656
|
G | T | 3 | a0001c0001t0003g0010a0001c0001t0003g0077a0001c0001t0021g0010 | 9 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-176+1936G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089656 | ||||||
chr6:112089825
|
A | G | 1 | a0001c0001t0007g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176+2105A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089825 | ||||||
chr6:112089830
|
C | T | 5 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(2): Show | 14 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-176+2110C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089830 | ||||||
chr6:112089857
|
C | T | 1 | a0001c0001t0019g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-176+2137C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089857 | ||||||
chr6:112089871
|
A | G | 19 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0010others(16): Show | 68 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-176+2151A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089871 | ||||||
chr6:112089979
|
G | C | 5 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(2): Show | 14 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-176+2259G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089979 | ||||||
chr6:112090047
|
A | G | 22 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(19): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-176+2327A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090047 | ||||||
chr6:112090064
|
A | G | 2 | a0001c0001t0003g0040a0001c0001t0003g0076 | 3 | NA18971.hp2 NA19062.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-176+2344A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090064 | ||||||
chr6:112090145
|
G | A | 2 | a0001c0001t0004g0024a0001c0001t0004g0028 | 5 | HG00438.hp2 HG02040.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176+2425G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090145 | ||||||
chr6:112090207
|
G | GTCTA | 30 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(27): Show | 127 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-176+2490_-176+249 others(8): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112090207 | |||||
chr6:112090479
|
G | A | 21 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(18): Show | 104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-176+2759G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090479 | ||||||
chr6:112090548
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0037 | 9 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-176+2828A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090548 | ||||||
chr6:112090567
|
ACAAT | A | 21 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(18): Show | 104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-176+2851_-176+285 others(8): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112090567 | |||||
chr6:112090749
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-176+3029T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090749 | ||||||
chr6:112090838
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-176+3118C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090838 | ||||||
chr6:112090856
|
G | A | 16 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(13): Show | 98 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-176+3136G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090856 | ||||||
chr6:112090980
|
G | T | 31 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-176+3260G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090980 | ||||||
chr6:112091000
|
C | T | 8 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(5): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-176+3280C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091000 | ||||||
chr6:112091017
|
TC | T | 8 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(5): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-176+3299delC | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112091017 | |||||
chr6:112091054
|
CTCTACTT others(1): Show |
C | 21 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(18): Show | 104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-176+3336_-176+334 others(12): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112091054 | |||||
chr6:112091092
|
C | A | 30 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(27): Show | 127 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-176+3372C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091092 | ||||||
chr6:112091382
|
T | C | 3 | a0001c0001t0004g0025a0001c0001t0004g0054a0001c0001t0004g0055 | 5 | HG01081.hp1 HG02723.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176+3662T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091382 | ||||||
chr6:112091479
|
G | C | 1 | a0001c0001t0006g0020 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176+3759G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091479 | ||||||
chr6:112091619
|
A | G | 1 | a0001c0001t0014g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-176+3899A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091619 | ||||||
chr6:112091785
|
T | G | 1 | a0001c0001t0019g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-176+4065T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091785 | ||||||
chr6:112091793
|
A | G | 2 | a0004c0004t0011g0027a0004c0004t0016g0044 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-176+4073A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091793 | ||||||
chr6:112091878
|
GAA | G | 16 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(13): Show | 98 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-176+4160_-176+416 others(6): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112091878 | |||||
chr6:112091975
|
G | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-176+4255G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091975 | ||||||
chr6:112092217
|
C | A | 18 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(15): Show | 101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-176+4497C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092217 | ||||||
chr6:112092259
|
G | A | 55 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(52): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-176+4539G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092259 | ||||||
chr6:112092313
|
T | G | 31 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-176+4593T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092313 | ||||||
chr6:112092634
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-175-4407A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092634 | ||||||
chr6:112092729
|
T | C | 3 | a0001c0001t0007g0086a0001c0001t0007g0087a0001c0001t0007g0088 | 3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-175-4312T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092729 | ||||||
chr6:112092767
|
A | C | 1 | a0001c0001t0004g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-175-4274A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092767 | ||||||
chr6:112092832
|
A | G | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-4209A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092832 | ||||||
chr6:112092842
|
G | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-4199G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092842 | ||||||
chr6:112092883
|
A | T | 1 | a0001c0001t0003g0075 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-175-4158A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092883 | ||||||
chr6:112093032
|
A | G | 1 | a0001c0001t0019g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-175-4009A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093032 | ||||||
chr6:112093040
|
G | A | 19 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0010others(16): Show | 68 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-175-4001G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093040 | ||||||
chr6:112093049
|
A | G | 31 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-175-3992A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093049 | ||||||
chr6:112093077
|
A | T | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-3964A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093077 | ||||||
chr6:112093107
|
A | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(15): Show | 101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-175-3934A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093107 | ||||||
chr6:112093222
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-175-3819C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093222 | ||||||
chr6:112093251
|
C | G | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-175-3790C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093251 | ||||||
chr6:112093252
|
A | T | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-175-3789A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093252 | ||||||
chr6:112093253
|
G | T | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-175-3788G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093253 | ||||||
chr6:112093558
|
C | T | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-175-3483C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093558 | ||||||
chr6:112093573
|
G | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(30): Show | 130 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-175-3468G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093573 | ||||||
chr6:112093658
|
G | A | 3 | a0001c0001t0007g0086a0001c0001t0007g0087a0001c0001t0007g0088 | 3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-175-3383G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093658 | ||||||
chr6:112093687
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0029 | 7 | NA18947.hp2 NA18961.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.-175-3354T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093687 | ||||||
chr6:112093730
|
A | G | 1 | a0004c0004t0016g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-175-3311A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093730 | ||||||
chr6:112093889
|
G | T | 2 | a0004c0004t0011g0027a0004c0004t0016g0044 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-175-3152G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093889 | ||||||
chr6:112094008
|
A | G | 3 | a0001c0001t0007g0086a0001c0001t0007g0087a0001c0001t0007g0088 | 3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-175-3033A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094008 | ||||||
chr6:112094026
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-175-3015A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094026 | ||||||
chr6:112094045
|
G | A | 2 | a0002c0002t0001g0030a0002c0002t0001g0031 | 4 | HG01884.hp2 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-175-2996G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094045 | ||||||
chr6:112094148
|
T | C | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-2893T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094148 | ||||||
chr6:112094244
|
G | C | 1 | a0001c0001t0019g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-175-2797G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094244 | ||||||
chr6:112094260
|
C | G | 22 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(19): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-175-2781C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094260 | ||||||
chr6:112094361
|
G | A | 8 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(5): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-2680G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094361 | ||||||
chr6:112094364
|
T | C | 1 | a0001c0001t0004g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-175-2677T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094364 | ||||||
chr6:112094446
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-175-2595C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094446 | ||||||
chr6:112094567
|
A | G | 3 | a0001c0001t0007g0086a0001c0001t0007g0087a0001c0001t0007g0088 | 3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-175-2474A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094567 | ||||||
chr6:112094817
|
A | G | 31 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-175-2224A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094817 | ||||||
chr6:112094982
|
A | G | 31 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-175-2059A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094982 | ||||||
chr6:112095043
|
A | G | 1 | a0001c0001t0004g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-175-1998A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095043 | ||||||
chr6:112095114
|
A | G | 33 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(30): Show | 130 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-175-1927A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095114 | ||||||
chr6:112095281
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-175-1760T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095281 | ||||||
chr6:112095426
|
A | G | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-175-1615A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095426 | ||||||
chr6:112095461
|
C | G | 55 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(52): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-175-1580C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095461 | ||||||
chr6:112095634
|
TCAAAAAA others(20): Show |
T | 1 | a0001c0001t0003g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-175-1390_-175-136 others(31): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095634 | |||||
chr6:112095635
|
C | CA | 22 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0023others(19): Show | 65 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-175-1381dupA | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | |||||
chr6:112095635
|
CA | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0003g0050others(4): Show | 21 | HG00408.hp2 HG00673.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-175-1381delA | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | |||||
chr6:112095635
|
CAA | C | 4 | a0001c0001t0005g0016a0001c0001t0005g0084a0001c0001t0019g0052others(1): Show | 10 | HG02055.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-175-1382_-175-138 others(6): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | |||||
chr6:112095635
|
CAAAAAA | C | 9 | a0001c0001t0002g0014a0001c0001t0002g0041a0001c0001t0002g0043others(6): Show | 15 | HG01243.hp1 HG01981.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.-175-1386_-175-138 others(10): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | |||||
chr6:112095635
|
CAAAAAAA | C | 8 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0015others(5): Show | 85 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-175-1387_-175-138 others(11): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | |||||
chr6:112095654
|
A | C | 2 | a0001c0001t0002g0083a0001c0001t0002g0089 | 2 | NA18965.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-175-1387A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095654 | ||||||
chr6:112095655
|
A | C | 2 | a0001c0001t0002g0083a0001c0001t0002g0089 | 2 | NA18965.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-175-1386A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095655 | ||||||
chr6:112095659
|
A | C | 1 | a0001c0001t0004g0067 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-175-1382A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095659 | ||||||
chr6:112095660
|
A | C | 1 | a0001c0001t0002g0079 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-175-1381A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095660 | ||||||
chr6:112095661
|
C | A | 1 | a0004c0004t0016g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-175-1380C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095661 | ||||||
chr6:112095662
|
C | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0091others(1): Show | 6 | HG01358.hp1 HG02738.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.-175-1379C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095662 | ||||||
chr6:112095663
|
A | C | 1 | a0004c0004t0016g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-175-1378A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095663 | ||||||
chr6:112095670
|
AAAAAAAA others(1): Show |
A | 7 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(4): Show | 17 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-175-1363_-175-135 others(12): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095670 | |||||
chr6:112095678
|
G | A | 22 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(19): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-175-1363G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095678 | ||||||
chr6:112095679
|
A | G | 22 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(19): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-175-1362A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095679 | ||||||
chr6:112095680
|
A | G | 8 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(5): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-1361A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095680 | ||||||
chr6:112095685
|
A | G | 1 | a0001c0001t0002g0082 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-175-1356A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095685 | ||||||
chr6:112095752
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-175-1289T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095752 | ||||||
chr6:112095844
|
G | A | 12 | a0001c0001t0004g0007a0001c0001t0004g0018a0001c0001t0004g0024others(9): Show | 36 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.-175-1197G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095844 | ||||||
chr6:112095993
|
G | C | 2 | a0001c0001t0005g0022a0001c0001t0005g0085 | 5 | HG01891.hp2 HG02257.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-175-1048G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095993 | ||||||
chr6:112096150
|
G | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(47): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-175-891G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096150 | ||||||
chr6:112096232
|
G | A | 1 | a0001c0001t0014g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-175-809G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096232 | ||||||
chr6:112096283
|
G | A | 8 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(5): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-758G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096283 | ||||||
chr6:112096339
|
G | A | 8 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(5): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-702G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096339 | ||||||
chr6:112096377
|
A | G | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-664A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096377 | ||||||
chr6:112096433
|
G | A | 1 | a0001c0001t0001g0036 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-175-608G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096433 | ||||||
chr6:112096474
|
T | TG | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-566dupG | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112096474 | |||||
chr6:112096479
|
A | G | 1 | a0001c0001t0006g0020 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-175-562A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096479 | ||||||
chr6:112096521
|
A | C | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-175-520A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096521 | ||||||
chr6:112096564
|
C | A | 2 | a0001c0001t0003g0039a0001c0001t0018g0039 | 2 | NA18939.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-175-477C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096564 | ||||||
chr6:112096687
|
T | TAAAGAAT others(309): Show |
1 | a0001c0001t0002g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-175-340_-175-339i others(318): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112096687 | |||||
chr6:112096777
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-175-264G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096777 | ||||||
chr6:112096791
|
A | T | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-175-250A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096791 | ||||||
chr6:112097020
|
T | C | 8 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(5): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-21T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112097020 | ||||||
chr6:112097035
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.-175-6C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112097035 | ||||||
chr6:112097257
|
G | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0038 | 9 | HG00099.hp1 HG01168.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+56G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097257 | ||||||
chr6:112097311
|
G | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-15+110G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097311 | ||||||
chr6:112097341
|
C | T | 1 | a0001c0001t0019g0052 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+140C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097341 | ||||||
chr6:112097439
|
A | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0064 | 3 | HG00621.hp1 NA18953.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-15+238A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097439 | ||||||
chr6:112097440
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0064 | 3 | HG00621.hp1 NA18953.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-15+239T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097440 | ||||||
chr6:112097482
|
GTACTAAT others(16): Show |
G | 1 | a0001c0001t0001g0046 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-15+304_-15+326del others(23): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 112097482 | |||||
chr6:112097520
|
TACATTGT others(16): Show |
T | 1 | a0001c0001t0003g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+360_-15+382del others(23): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 112097520 | |||||
chr6:112097570
|
T | TTGTGTAC others(16): Show |
2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+391_-15+392ins others(23): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 112097570 | |||||
chr6:112097593
|
T | C | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+392T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097593 | ||||||
chr6:112097620
|
G | A | 1 | a0001c0001t0007g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15+419G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097620 | ||||||
chr6:112097660
|
CAG | C | 21 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(18): Show | 104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-15+460_-15+461del others(2): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097660 | ||||||
chr6:112097671
|
A | G | 2 | a0001c0001t0010g0056a0001c0001t0010g0057 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+470A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097671 | ||||||
chr6:112097686
|
T | G | 1 | a0001c0001t0002g0026 | 3 | HG01109.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-15+485T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097686 | ||||||
chr6:112097776
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-15+575A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097776 | ||||||
chr6:112097863
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-15+662C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097863 | ||||||
chr6:112097960
|
A | T | 1 | a0001c0001t0003g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+759A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097960 | ||||||
chr6:112098050
|
G | A | 8 | a0001c0001t0002g0003a0001c0001t0002g0015a0001c0001t0002g0041others(5): Show | 46 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+849G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098050 | ||||||
chr6:112098203
|
G | A | 8 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(5): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-15+1002G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098203 | ||||||
chr6:112098268
|
C | T | 1 | a0001c0001t0006g0020 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1002C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098268 | ||||||
chr6:112098274
|
C | A | 1 | a0001c0001t0003g0074 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-14-996C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098274 | ||||||
chr6:112098306
|
T | A | 33 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(30): Show | 130 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-14-964T>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098306 | ||||||
chr6:112098399
|
A | G | 1 | a0001c0001t0004g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14-871A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098399 | ||||||
chr6:112098461
|
C | T | 21 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(18): Show | 104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-14-809C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098461 | ||||||
chr6:112098502
|
A | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0080 | 7 | HG02074.hp2 NA18960.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-768A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098502 | ||||||
chr6:112098607
|
C | T | 1 | a0001c0001t0006g0020 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-663C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098607 | ||||||
chr6:112098801
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG01071.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-14-469C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098801 | ||||||
chr6:112098849
|
G | A | 31 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-14-421G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098849 | ||||||
chr6:112098927
|
A | G | 1 | a0001c0001t0007g0087 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-14-343A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098927 | ||||||
chr6:112099024
|
T | C | 16 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(13): Show | 98 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-14-246T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099024 | ||||||
chr6:112099053
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-14-217G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099053 | ||||||
chr6:112099086
|
G | T | 1 | a0001c0001t0014g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14-184G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099086 | ||||||
chr6:112099183
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0059 | 5 | HG01168.hp2 HG01169.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-87A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099183 | ||||||
chr6:112099241
|
G | A | 5 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(2): Show | 14 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-29G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099241 | ||||||
chr6:112099482
|
T | G | 31 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.125+74T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112099482 | ||||||
chr6:112099500
|
T | C | 31 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(28): Show | 128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.125+92T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112099500 | ||||||
chr6:112099812
|
C | A | 8 | a0001c0001t0005g0016a0001c0001t0005g0022a0001c0001t0005g0042others(5): Show | 18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.125+404C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112099812 | ||||||
chr6:112099855
|
G | A | 1 | a0001c0001t0014g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.125+447G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112099855 | ||||||
chr6:112100102
|
C | T | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.126-568C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100102 | ||||||
chr6:112100117
|
C | T | 55 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(52): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.126-553C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100117 | ||||||
chr6:112100518
|
C | T | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0014others(20): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.126-152C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100518 | ||||||
chr6:112100519
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.126-151G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100519 | ||||||
chr6:112100602
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0033others(3): Show | 31 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-68T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100602 |