geneid | 90525 |
---|---|
ensemblid | ENSG00000138606.20 |
hgncid | 25116 |
symbol | SHF |
name | Src homology 2 domain containing F |
refseq_nuc | NM_001394037.1 |
refseq_prot | NP_001380966.1 |
ensembl_nuc | ENST00000690270.1 |
ensembl_prot | ENSP00000508579.1 |
mane_status | MANE Select |
chr | chr15 |
start | 45167214 |
end | 45187966 |
strand | - |
ver | v1.2 |
region | chr15:45167214-45187966 |
region5000 | chr15:45162214-45192966 |
regionname0 | SHF_chr15_45167214_45187966 |
regionname5000 | SHF_chr15_45162214_45192966 |
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 | 0/1 | 488 | 338 | 91 | 66 | 130 | 10 | 40 | 94 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0002 | 1/0 | 488 | 56 | 1 | 5 | 49 | 0 | 0 | 39 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0003 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0004 | 0/0 | 434 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0005 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0006 | 0/0 | 488 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
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 | 0/1 | 1467 | 336 | 89 | 66 | 130 | 10 | 40 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
c0002 | 1/0 | 1467 | 42 | 1 | 5 | 35 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
c0003 | 0/0 | 1467 | 14 | 0 | 0 | 14 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
c0004 | 0/0 | 1467 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
c0005 | 0/0 | 1467 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
c0006 | 0/0 | 1466 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
c0007 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
c0008 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
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 | 1/0 | 749 | 165 | 49 | 14 | 90 | 0 | 11 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
t0002 | 0/1 | 749 | 162 | 24 | 51 | 60 | 9 | 17 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
t0003 | 0/0 | 749 | 60 | 16 | 3 | 30 | 1 | 10 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
t0004 | 0/0 | 749 | 4 | 2 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
t0005 | 0/0 | 749 | 2 | 0 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
t0006 | 0/0 | 749 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
t0007 | 0/0 | 749 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
t0008 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
t0009 | 0/0 | 749 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
t0010 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 33 | 0 | 4 | 26 | 0 | 3 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0002 | 0/0 | 28 | 0 | 4 | 24 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0003 | 0/0 | 28 | 1 | 9 | 15 | 1 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0004 | 0/0 | 28 | 2 | 3 | 18 | 1 | 4 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0005 | 0/0 | 23 | 0 | 1 | 22 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0006 | 0/1 | 16 | 0 | 7 | 4 | 1 | 3 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0007 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0008 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0009 | 0/0 | 8 | 2 | 2 | 0 | 1 | 3 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0010 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0012 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0020 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0044 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
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 | 0/1 | 1467 | 336 | 89 | 66 | 130 | 10 | 40 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0004 | 0/0 | 1467 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0002c0002 | 1/0 | 1467 | 42 | 1 | 5 | 35 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0002c0003 | 0/0 | 1467 | 14 | 0 | 0 | 14 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0003c0008 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0004c0006 | 0/0 | 1466 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0005c0007 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0006c0005 | 0/0 | 1467 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2215 | 109 | 48 | 9 | 41 | 0 | 11 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0001t0002 | 0/1 | 2215 | 156 | 22 | 50 | 57 | 9 | 17 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0001t0003 | 0/0 | 2215 | 60 | 16 | 3 | 30 | 1 | 10 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0001t0004 | 0/0 | 2215 | 4 | 2 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0001t0005 | 0/0 | 2215 | 2 | 0 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0001t0006 | 0/0 | 2215 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0001t0007 | 0/0 | 2215 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0001t0008 | 0/0 | 2215 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0001t0009 | 0/0 | 2215 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0001t0010 | 0/0 | 2215 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0001c0004t0002 | 0/0 | 2215 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0002c0002t0001 | 1/0 | 2215 | 42 | 1 | 5 | 35 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0002c0003t0001 | 0/0 | 2215 | 14 | 0 | 0 | 14 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0003c0008t0002 | 0/0 | 2215 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0004c0006t0002 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0005c0007t0002 | 0/0 | 2215 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
a0006c0005t0002 | 0/0 | 2215 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | copy fasta | chr15 | 45162214 | 45192966 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 33 | 0 | 4 | 26 | 0 | 3 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0003 | 0/0 | 28 | 1 | 9 | 15 | 1 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0005 | 0/0 | 23 | 0 | 1 | 22 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0006 | 0/1 | 16 | 0 | 7 | 4 | 1 | 3 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0008 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0009 | 0/0 | 8 | 2 | 2 | 0 | 1 | 3 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0010 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0012 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0004 | 0/0 | 28 | 2 | 3 | 18 | 1 | 4 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0044 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0004g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0005g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0001c0004t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0002 | 0/0 | 28 | 0 | 4 | 24 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0003t0001g0007 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0003c0008t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0004c0006t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0005c0007t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
a0006c0005t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | GBR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | GBR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | GBR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | GBR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | FIN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00558 | hp2 | a0001 | c0001 | t0008 | g0130 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00639 | hp1 | a0006 | c0005 | t0002 | g0091 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0132 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0103 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03225 | hp1 | a0001 | c0004 | t0002 | g0047 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0034 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0082 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | CHB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18941 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18949 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18968 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18981 | hp1 | a0005 | c0007 | t0002 | g0102 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18991 | hp1 | a0001 | c0001 | t0010 | g0137 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18992 | hp1 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18995 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18997 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19043 | hp1 | a0001 | c0004 | t0002 | g0047 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19055 | hp2 | a0004 | c0006 | t0002 | g0098 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19063 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19067 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19078 | hp2 | a0003 | c0008 | t0002 | g0052 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19079 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19081 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ASW | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | TSI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | USA | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | USA | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0006 | REF | REF | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0062 | REF | REF | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:45167951
|
A | C | 1 | a0005 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1463T>G | p.Leu488Arg | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 1478/2215 | 1463/1467 | 488/488 | chr15 | 45167951 | ||
chr15:45168132
|
TCCTGGGA others(6): Show |
T | 1 | a0004 | 1 | NA19055.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1281-12_1281delTCC others(10): Show |
p.Ser428fs | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 1296/2215 | 1281/1467 | 427/488 | chr15 | 45168132 | ||
chr15:45172312
|
A | G | 1 | a0006 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.995T>C | p.Phe332Ser | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 5/7 | 1010/2215 | 995/1467 | 332/488 | chr15 | 45172312 | ||
chr15:45175342
|
C | G | 5 | a0001a0003a0004others(2): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
missense_variant | MODERATE | c.724G>C | p.Ala242Pro | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/7 | 739/2215 | 724/1467 | 242/488 | chr15 | 45175342 | ||
chr15:45175419
|
C | G | 1 | a0003 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.647G>C | p.Arg216Pro | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/7 | 662/2215 | 647/1467 | 216/488 | chr15 | 45175419 | ||
chr15:45175420
|
G | C | 1 | a0003 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.646C>G | p.Arg216Gly | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/7 | 661/2215 | 646/1467 | 216/488 | chr15 | 45175420 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:45175343
|
G | A | 1 | a0002c0003 | 14 | NA18941.hp1 NA18949.hp1 NA18953.hp1 others(11): Show |
synonymous_variant | LOW | c.723C>T | p.Thr241Thr | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/7 | 738/2215 | 723/1467 | 241/488 | chr15 | 45175343 | ||
chr15:45178271
|
A | G | 1 | a0001c0004 | 2 | HG03225.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.534T>C | p.Asp178Asp | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/7 | 549/2215 | 534/1467 | 178/488 | chr15 | 45178271 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:45167360
|
G | A | 1 | a0001c0001t0007 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*587C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 587 | chr15 | 45167360 | |||||
chr15:45167366
|
G | A | 10 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(7): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*581C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 581 | chr15 | 45167366 | |||||
chr15:45167439
|
C | G | 1 | a0001c0001t0007 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*508G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 508 | chr15 | 45167439 | |||||
chr15:45167534
|
G | A | 1 | a0001c0001t0008 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*413C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 413 | chr15 | 45167534 | |||||
chr15:45167587
|
C | A | 1 | a0001c0001t0009 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 360 | chr15 | 45167587 | |||||
chr15:45167675
|
C | T | 1 | a0001c0001t0006 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 272 | chr15 | 45167675 | |||||
chr15:45167773
|
C | G | 1 | a0001c0001t0003 | 60 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*174G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 174 | chr15 | 45167773 | |||||
chr15:45167774
|
C | A | 1 | a0001c0001t0010 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 173 | chr15 | 45167774 | |||||
chr15:45167792
|
T | C | 1 | a0001c0001t0004 | 4 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*155A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 155 | chr15 | 45167792 | |||||
chr15:45187965
|
C | A | 1 | a0001c0001t0005 | 2 | HG00642.hp2 HG01358.hp1 |
5_prime_UTR_variant | MODIFIER | c.-14G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/7 | 14 | chr15 | 45187965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:45168224
|
A | G | 73 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0041others(70): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1281-91T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168224 | ||||||
chr15:45168386
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1281-253C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168386 | ||||||
chr15:45168404
|
C | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0030others(44): Show | 120 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1281-271G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168404 | ||||||
chr15:45168435
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1281-302A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168435 | ||||||
chr15:45168480
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1281-347C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168480 | ||||||
chr15:45168527
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0070others(4): Show | 8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281-394G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168527 | ||||||
chr15:45168530
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0065others(5): Show | 11 | HG00642.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1281-397C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168530 | ||||||
chr15:45169180
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1281-1047G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169180 | ||||||
chr15:45169203
|
A | G | 24 | a0001c0001t0001g0041a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.1281-1070T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169203 | ||||||
chr15:45169559
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0070others(4): Show | 8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281-1426G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169559 | ||||||
chr15:45169856
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1281-1723C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169856 | ||||||
chr15:45169893
|
C | G | 1 | a0001c0001t0003g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1281-1760G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169893 | ||||||
chr15:45170241
|
C | T | 8 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0073others(5): Show | 17 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1280+1642G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170241 | ||||||
chr15:45170383
|
C | T | 1 | a0001c0001t0001g0011 | 5 | HG01496.hp2 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+1500G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170383 | ||||||
chr15:45170486
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1280+1397C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170486 | ||||||
chr15:45170538
|
C | T | 4 | a0001c0001t0002g0008a0001c0001t0002g0123a0001c0001t0004g0018others(1): Show | 15 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1280+1345G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170538 | ||||||
chr15:45170645
|
C | CT | 4 | a0001c0001t0001g0116a0001c0001t0001g0146a0001c0001t0002g0021others(1): Show | 6 | HG00741.hp2 HG01081.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+1237dupA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170645 | ||||||
chr15:45170645
|
CT | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(70): Show | 195 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1280+1237delA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170645 | ||||||
chr15:45170645
|
CTT | C | 8 | a0001c0001t0001g0067a0001c0001t0001g0081a0001c0001t0001g0088others(5): Show | 11 | HG02451.hp1 HG02896.hp1 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.1280+1236_1280+123 others(6): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170645 | ||||||
chr15:45170649
|
T | C | 36 | a0001c0001t0001g0050a0001c0001t0001g0108a0001c0001t0002g0003others(33): Show | 107 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1280+1234A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170649 | ||||||
chr15:45170650
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1280+1233A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170650 | ||||||
chr15:45170653
|
T | C | 1 | a0001c0001t0002g0092 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1280+1230A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170653 | ||||||
chr15:45170747
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0004g0018a0001c0001t0004g0078 | 14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1280+1136C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170747 | ||||||
chr15:45170758
|
TTTCCTGC others(14): Show |
T | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+1104_1280+112 others(25): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170758 | ||||||
chr15:45170843
|
G | T | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+1040C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170843 | ||||||
chr15:45170863
|
G | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0023others(51): Show | 131 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1280+1020C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170863 | ||||||
chr15:45170903
|
C | T | 3 | a0001c0001t0002g0051a0001c0001t0002g0101a0003c0008t0002g0052 | 3 | NA18993.hp1 NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1280+980G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170903 | ||||||
chr15:45170996
|
A | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0055 | 3 | HG01109.hp1 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1280+887T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170996 | ||||||
chr15:45171082
|
A | G | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+801T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171082 | ||||||
chr15:45171083
|
T | A | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+800A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171083 | ||||||
chr15:45171084
|
G | T | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+799C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171084 | ||||||
chr15:45171117
|
A | T | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+766T>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171117 | ||||||
chr15:45171122
|
G | C | 1 | a0001c0001t0002g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1280+761C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171122 | ||||||
chr15:45171298
|
C | T | 1 | a0001c0001t0002g0042 | 2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1280+585G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171298 | ||||||
chr15:45171357
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0065others(1): Show | 7 | HG00642.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280+526T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171357 | ||||||
chr15:45171426
|
C | G | 24 | a0001c0001t0001g0041a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.1280+457G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171426 | ||||||
chr15:45171438
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1280+445G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171438 | ||||||
chr15:45171692
|
A | G | 3 | a0001c0001t0002g0008a0001c0001t0004g0018a0001c0001t0004g0078 | 14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1280+191T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171692 | ||||||
chr15:45172378
|
T | C | 1 | a0001c0001t0001g0030 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.989-60A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172378 | ||||||
chr15:45172467
|
G | C | 1 | a0001c0001t0002g0095 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.989-149C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172467 | ||||||
chr15:45172570
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(125): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.989-252T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172570 | ||||||
chr15:45172804
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.989-486C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172804 | ||||||
chr15:45172836
|
G | C | 60 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(57): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.989-518C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172836 | ||||||
chr15:45172845
|
C | T | 8 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0073others(5): Show | 17 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.989-527G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172845 | ||||||
chr15:45172918
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.989-600C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172918 | ||||||
chr15:45172959
|
G | C | 1 | a0001c0001t0003g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.988+617C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172959 | ||||||
chr15:45172960
|
T | C | 1 | a0001c0001t0003g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.988+616A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172960 | ||||||
chr15:45172962
|
G | T | 1 | a0001c0001t0003g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.988+614C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172962 | ||||||
chr15:45172980
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.988+596G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172980 | ||||||
chr15:45172995
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0065others(5): Show | 11 | HG00642.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.988+581C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172995 | ||||||
chr15:45172995
|
G | T | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.988+581C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172995 | ||||||
chr15:45173053
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0025others(118): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.988+523C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173053 | ||||||
chr15:45173085
|
T | A | 1 | a0001c0001t0003g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.988+491A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173085 | ||||||
chr15:45173134
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0068 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.988+442C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173134 | ||||||
chr15:45173335
|
T | A | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.988+241A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173335 | ||||||
chr15:45173388
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.988+188G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173388 | ||||||
chr15:45173453
|
C | G | 1 | a0001c0001t0003g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.988+123G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173453 | ||||||
chr15:45173457
|
A | C | 1 | a0002c0002t0001g0061 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.988+119T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173457 | ||||||
chr15:45173538
|
G | T | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.988+38C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173538 | ||||||
chr15:45173794
|
C | A | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-78G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45173794 | ||||||
chr15:45173832
|
GGGCAGA | G | 4 | a0001c0001t0002g0009a0001c0001t0002g0120a0001c0001t0002g0126others(1): Show | 11 | HG00099.hp2 HG00140.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.848-122_848-117del others(6): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45173832 | ||||||
chr15:45173897
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0004g0018a0001c0001t0004g0078 | 14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.848-181G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45173897 | ||||||
chr15:45173996
|
T | G | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-280A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45173996 | ||||||
chr15:45174211
|
T | C | 23 | a0001c0001t0001g0041a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.848-495A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174211 | ||||||
chr15:45174234
|
A | G | 23 | a0001c0001t0001g0041a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.848-518T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174234 | ||||||
chr15:45174273
|
C | T | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-557G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174273 | ||||||
chr15:45174274
|
T | C | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-558A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174274 | ||||||
chr15:45174278
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0148 | 2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.848-562C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174278 | ||||||
chr15:45174281
|
T | G | 1 | a0003c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-565A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174281 | ||||||
chr15:45174463
|
C | A | 3 | a0001c0001t0002g0008a0001c0001t0004g0018a0001c0001t0004g0078 | 14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.848-747G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174463 | ||||||
chr15:45174532
|
A | T | 1 | a0001c0001t0003g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.847+687T>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174532 | ||||||
chr15:45174646
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.847+573G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174646 | ||||||
chr15:45174750
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0068 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.847+469T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174750 | ||||||
chr15:45174894
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(98): Show | 252 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.847+325T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174894 | ||||||
chr15:45175075
|
C | G | 1 | a0001c0001t0003g0138 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.847+144G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45175075 | ||||||
chr15:45175543
|
G | C | 1 | a0001c0001t0002g0074 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.641-118C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175543 | ||||||
chr15:45175600
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.641-175G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175600 | ||||||
chr15:45175611
|
A | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0057others(6): Show | 12 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-186T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175611 | ||||||
chr15:45175819
|
CT | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0113a0001c0001t0001g0121others(2): Show | 6 | HG02109.hp1 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.641-395delA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175819 | ||||||
chr15:45175819
|
CTT | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0022others(116): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.641-396_641-395del others(2): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175819 | ||||||
chr15:45175819
|
CTTT | C | 5 | a0001c0001t0001g0025a0001c0001t0002g0008a0001c0001t0002g0043others(2): Show | 18 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.641-397_641-395del others(3): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175819 | ||||||
chr15:45175826
|
T | C | 45 | a0001c0001t0001g0019a0001c0001t0001g0057a0001c0001t0001g0070others(42): Show | 118 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.641-401A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175826 | ||||||
chr15:45175827
|
T | C | 1 | a0001c0001t0001g0025 | 2 | HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.641-402A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175827 | ||||||
chr15:45175841
|
C | T | 21 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0021others(18): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.641-416G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175841 | ||||||
chr15:45175905
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.641-480C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175905 | ||||||
chr15:45175936
|
A | G | 1 | a0001c0001t0007g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.641-511T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175936 | ||||||
chr15:45175967
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.641-542G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175967 | ||||||
chr15:45176336
|
T | C | 1 | a0001c0001t0007g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.641-911A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176336 | ||||||
chr15:45176428
|
T | C | 73 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0041others(70): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.641-1003A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176428 | ||||||
chr15:45176551
|
T | C | 1 | a0001c0001t0003g0140 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.641-1126A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176551 | ||||||
chr15:45176656
|
C | T | 1 | a0001c0001t0001g0011 | 5 | HG01496.hp2 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-1231G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176656 | ||||||
chr15:45176713
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.641-1288A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176713 | ||||||
chr15:45176751
|
A | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0057others(6): Show | 12 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-1326T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176751 | ||||||
chr15:45176839
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.640+1326A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176839 | ||||||
chr15:45177111
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.640+1054C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177111 | ||||||
chr15:45177253
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.640+912C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177253 | ||||||
chr15:45177288
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0145 | 4 | HG03209.hp1 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+877G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177288 | ||||||
chr15:45177413
|
C | CT | 6 | a0001c0001t0003g0045a0001c0001t0003g0131a0001c0001t0003g0135others(3): Show | 7 | HG00423.hp2 HG02132.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+751dupA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177413 | ||||||
chr15:45177435
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.640+730T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177435 | ||||||
chr15:45177496
|
C | G | 37 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0002g0005others(34): Show | 107 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.640+669G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177496 | ||||||
chr15:45177545
|
C | T | 33 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0026others(30): Show | 74 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.640+620G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177545 | ||||||
chr15:45177650
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.640+515G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177650 | ||||||
chr15:45177689
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.640+476G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177689 | ||||||
chr15:45177836
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.640+329A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177836 | ||||||
chr15:45177853
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0004g0018a0001c0001t0004g0078 | 14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.640+312G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177853 | ||||||
chr15:45177874
|
T | A | 1 | a0001c0001t0003g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.640+291A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177874 | ||||||
chr15:45178105
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.640+60G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45178105 | ||||||
chr15:45178352
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-46G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178352 | ||||||
chr15:45178511
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.499-205T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178511 | ||||||
chr15:45178534
|
C | CT | 60 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0022others(57): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.499-229dupA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178534 | ||||||
chr15:45178534
|
CT | C | 8 | a0001c0001t0002g0033a0001c0001t0002g0096a0001c0001t0002g0097others(5): Show | 9 | HG01070.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.499-229delA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178534 | ||||||
chr15:45178565
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.499-259G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178565 | ||||||
chr15:45178575
|
C | T | 1 | a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.499-269G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178575 | ||||||
chr15:45178604
|
G | A | 1 | a0002c0002t0001g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.499-298C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178604 | ||||||
chr15:45178684
|
A | G | 5 | a0001c0001t0002g0012a0001c0001t0002g0020a0001c0001t0002g0033others(2): Show | 12 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.499-378T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178684 | ||||||
chr15:45178723
|
T | C | 6 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0147others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-417A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178723 | ||||||
chr15:45178725
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.499-419C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178725 | ||||||
chr15:45178779
|
C | T | 1 | a0001c0001t0002g0035 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.499-473G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178779 | ||||||
chr15:45178813
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0004g0018a0001c0001t0004g0078 | 14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-507C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178813 | ||||||
chr15:45178824
|
C | T | 1 | a0002c0002t0001g0059 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.499-518G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178824 | ||||||
chr15:45178825
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.499-519C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178825 | ||||||
chr15:45178851
|
C | G | 7 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0070others(4): Show | 8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-545G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178851 | ||||||
chr15:45178948
|
C | G | 1 | a0001c0001t0003g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.499-642G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178948 | ||||||
chr15:45179039
|
T | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0070others(4): Show | 8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-733A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179039 | ||||||
chr15:45179285
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.499-979A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179285 | ||||||
chr15:45179291
|
C | T | 21 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0021others(18): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.499-985G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179291 | ||||||
chr15:45179444
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.499-1138A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179444 | ||||||
chr15:45179487
|
TG | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(141): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.499-1182delC | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179487 | ||||||
chr15:45179724
|
G | C | 1 | a0001c0001t0003g0142 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.499-1418C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179724 | ||||||
chr15:45179851
|
G | A | 3 | a0001c0001t0003g0039a0001c0001t0003g0114a0001c0001t0003g0115 | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-1545C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179851 | ||||||
chr15:45180077
|
G | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0110 | 2 | HG02683.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.499-1771C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180077 | ||||||
chr15:45180252
|
C | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0109 | 8 | HG01074.hp2 HG01257.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-1946G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180252 | ||||||
chr15:45180373
|
G | A | 1 | a0001c0001t0002g0105 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.499-2067C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180373 | ||||||
chr15:45180512
|
A | G | 36 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0041others(33): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
intron_variant | MODIFIER | c.499-2206T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180512 | ||||||
chr15:45180683
|
T | C | 15 | a0001c0001t0001g0108a0001c0001t0002g0003a0001c0001t0002g0015others(12): Show | 46 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.499-2377A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180683 | ||||||
chr15:45180845
|
T | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0057others(6): Show | 12 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.499-2539A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180845 | ||||||
chr15:45180947
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0065others(1): Show | 7 | HG00642.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-2641C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180947 | ||||||
chr15:45181021
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.499-2715G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181021 | ||||||
chr15:45181030
|
C | G | 1 | a0001c0001t0003g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.499-2724G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181030 | ||||||
chr15:45181111
|
G | A | 1 | a0001c0001t0001g0032 | 2 | NA18995.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.499-2805C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181111 | ||||||
chr15:45181145
|
G | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0022others(129): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.499-2839C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181145 | ||||||
chr15:45181153
|
C | T | 1 | a0002c0002t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.499-2847G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181153 | ||||||
chr15:45181308
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0068 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.499-3002G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181308 | ||||||
chr15:45181412
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(20): Show | 61 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.499-3106G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181412 | ||||||
chr15:45181482
|
G | A | 1 | a0001c0001t0002g0105 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.499-3176C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181482 | ||||||
chr15:45181553
|
T | G | 1 | a0001c0001t0002g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.499-3247A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181553 | ||||||
chr15:45181636
|
C | A | 1 | a0001c0001t0007g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.499-3330G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181636 | ||||||
chr15:45181744
|
T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG02615.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.499-3438A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181744 | ||||||
chr15:45181768
|
A | G | 1 | a0001c0001t0003g0132 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.499-3462T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181768 | ||||||
chr15:45181782
|
G | C | 1 | a0001c0001t0003g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.499-3476C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181782 | ||||||
chr15:45181840
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0068 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.499-3534T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181840 | ||||||
chr15:45181858
|
A | G | 1 | a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.499-3552T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181858 | ||||||
chr15:45181877
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.499-3571C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181877 | ||||||
chr15:45181889
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.499-3583C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181889 | ||||||
chr15:45181911
|
G | C | 20 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0021others(17): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.499-3605C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181911 | ||||||
chr15:45181953
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0065others(1): Show | 7 | HG00642.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-3647T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181953 | ||||||
chr15:45182111
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.499-3805G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182111 | ||||||
chr15:45182173
|
A | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0019others(75): Show | 201 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.499-3867T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182173 | ||||||
chr15:45182209
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0053 | 6 | HG02486.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-3903C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182209 | ||||||
chr15:45182252
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.499-3946C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182252 | ||||||
chr15:45182533
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0050others(1): Show | 7 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.499-4227G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182533 | ||||||
chr15:45182739
|
T | C | 14 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0065others(11): Show | 17 | HG00642.hp1 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.499-4433A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182739 | ||||||
chr15:45182743
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.499-4437T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182743 | ||||||
chr15:45183037
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.498+4417A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183037 | ||||||
chr15:45183157
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.498+4297C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183157 | ||||||
chr15:45183305
|
T | C | 25 | a0001c0001t0001g0041a0001c0001t0001g0116a0001c0001t0001g0117others(22): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.498+4149A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183305 | ||||||
chr15:45183332
|
CAT | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0022others(94): Show | 256 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.498+4120_498+4121d others(4): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183332 | ||||||
chr15:45183416
|
CA | C | 10 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0145others(7): Show | 13 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.498+4037delT | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183416 | ||||||
chr15:45183504
|
T | C | 1 | a0002c0002t0001g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.498+3950A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183504 | ||||||
chr15:45183528
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.498+3926C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183528 | ||||||
chr15:45183536
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.498+3918C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183536 | ||||||
chr15:45183543
|
G | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0145others(7): Show | 13 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.498+3911C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183543 | ||||||
chr15:45183565
|
A | G | 2 | a0001c0001t0004g0018a0001c0001t0004g0078 | 4 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+3889T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183565 | ||||||
chr15:45183597
|
T | G | 2 | a0001c0001t0001g0070a0001c0001t0002g0071 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.498+3857A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183597 | ||||||
chr15:45183618
|
G | C | 40 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0046others(37): Show | 89 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.498+3836C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183618 | ||||||
chr15:45183618
|
G | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0030others(54): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.498+3836C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183618 | ||||||
chr15:45183667
|
C | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0145others(8): Show | 14 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+3787G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183667 | ||||||
chr15:45183882
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.498+3572G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183882 | ||||||
chr15:45184230
|
T | A | 3 | a0001c0001t0002g0008a0001c0001t0004g0018a0001c0001t0004g0078 | 14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+3224A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184230 | ||||||
chr15:45184321
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0022others(117): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.498+3133G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184321 | ||||||
chr15:45184463
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0145others(8): Show | 14 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+2991C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184463 | ||||||
chr15:45184539
|
G | T | 1 | a0001c0001t0002g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.498+2915C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184539 | ||||||
chr15:45184543
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0022others(113): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.498+2911C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184543 | ||||||
chr15:45184754
|
C | T | 7 | a0001c0001t0001g0029a0001c0001t0001g0081a0001c0001t0002g0008others(4): Show | 19 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.498+2700G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184754 | ||||||
chr15:45184801
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.498+2653A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184801 | ||||||
chr15:45184814
|
A | G | 47 | a0001c0001t0001g0041a0001c0001t0001g0116a0001c0001t0001g0117others(44): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.498+2640T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184814 | ||||||
chr15:45184846
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.498+2608G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184846 | ||||||
chr15:45185126
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.498+2328C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185126 | ||||||
chr15:45185290
|
T | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG02965.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.498+2164A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185290 | ||||||
chr15:45185293
|
T | A | 1 | a0001c0001t0003g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+2161A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185293 | ||||||
chr15:45185330
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.498+2124G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185330 | ||||||
chr15:45185465
|
T | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0145others(8): Show | 14 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+1989A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185465 | ||||||
chr15:45185512
|
C | T | 1 | a0001c0001t0003g0040 | 2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.498+1942G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185512 | ||||||
chr15:45185752
|
G | A | 1 | a0001c0001t0003g0016 | 4 | HG02630.hp2 HG02717.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1702C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185752 | ||||||
chr15:45186076
|
A | C | 1 | a0001c0001t0003g0079 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.498+1378T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186076 | ||||||
chr15:45186121
|
C | T | 3 | a0001c0001t0003g0039a0001c0001t0003g0114a0001c0001t0003g0115 | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1333G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186121 | ||||||
chr15:45186158
|
G | A | 1 | a0001c0001t0003g0038 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.498+1296C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186158 | ||||||
chr15:45186180
|
C | A | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG02965.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.498+1274G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186180 | ||||||
chr15:45186184
|
G | T | 1 | a0002c0003t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.498+1270C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186184 | ||||||
chr15:45186185
|
A | G | 1 | a0002c0003t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.498+1269T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186185 | ||||||
chr15:45186187
|
C | A | 1 | a0002c0003t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.498+1267G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186187 | ||||||
chr15:45186253
|
G | A | 1 | a0002c0003t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.498+1201C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186253 | ||||||
chr15:45186385
|
T | C | 47 | a0001c0001t0001g0041a0001c0001t0001g0116a0001c0001t0001g0117others(44): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.498+1069A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186385 | ||||||
chr15:45186416
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0004g0018a0001c0001t0004g0078 | 14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+1038G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186416 | ||||||
chr15:45186451
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.498+1003G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186451 | ||||||
chr15:45186463
|
G | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0145others(7): Show | 13 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.498+991C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186463 | ||||||
chr15:45186523
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.498+931G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186523 | ||||||
chr15:45186603
|
A | C | 1 | a0001c0001t0002g0075 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.498+851T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186603 | ||||||
chr15:45186745
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.498+709A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186745 | ||||||
chr15:45186970
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.498+484G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186970 | ||||||
chr15:45187134
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG01081.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.498+320G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187134 | ||||||
chr15:45187153
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0022others(120): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.498+301A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187153 | ||||||
chr15:45187198
|
G | A | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0004t0002g0047 | 4 | HG00642.hp1 HG03225.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+256C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187198 | ||||||
chr15:45187200
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.498+254C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187200 | ||||||
chr15:45187325
|
T | C | 2 | a0001c0001t0001g0158a0002c0002t0001g0157 | 2 | HG00558.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.498+129A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187325 | ||||||
chr15:45187358
|
C | G | 1 | a0002c0003t0001g0049 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.498+96G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187358 |