geneid | 6668 |
---|---|
ensemblid | ENSG00000167182.16 |
hgncid | 11207 |
symbol | SP2 |
name | Sp2 transcription factor |
refseq_nuc | NM_003110.6 |
refseq_prot | NP_003101.3 |
ensembl_nuc | ENST00000376741.5 |
ensembl_prot | ENSP00000365931.4 |
mane_status | MANE Select |
chr | chr17 |
start | 47896236 |
end | 47928957 |
strand | + |
ver | v1.2 |
region | chr17:47896236-47928957 |
region5000 | chr17:47891236-47933957 |
regionname0 | SP2_chr17_47896236_47928957 |
regionname5000 | SP2_chr17_47891236_47933957 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 613 | 321 | 85 | 61 | 123 | 15 | 35 | 100 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0002 | 0/0 | 613 | 35 | 2 | 16 | 10 | 1 | 6 | 9 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0003 | 0/0 | 613 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0004 | 0/0 | 613 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0005 | 0/0 | 606 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0006 | 0/0 | 613 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
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 | 1842 | 173 | 32 | 25 | 89 | 9 | 17 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0002 | 1/0 | 1842 | 122 | 30 | 35 | 32 | 6 | 18 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0003 | 0/0 | 1842 | 32 | 2 | 16 | 7 | 1 | 6 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0004 | 0/0 | 1842 | 19 | 19 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0005 | 0/0 | 1842 | 5 | 4 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0006 | 0/0 | 1842 | 4 | 3 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0007 | 0/0 | 1842 | 4 | 0 | 0 | 4 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0008 | 0/0 | 1842 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0009 | 0/0 | 1842 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0010 | 0/0 | 1842 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0011 | 0/0 | 1842 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
c0012 | 0/0 | 1842 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
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 | 0/1 | 1187 | 191 | 44 | 24 | 95 | 10 | 17 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
t0002 | 1/0 | 1185 | 155 | 40 | 42 | 41 | 6 | 25 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
t0003 | 0/0 | 1185 | 6 | 0 | 6 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
t0004 | 0/0 | 1186 | 6 | 1 | 4 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
t0005 | 0/0 | 1187 | 4 | 3 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
t0006 | 0/0 | 1188 | 3 | 1 | 1 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
t0007 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
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 | 27 | 2 | 1 | 19 | 2 | 3 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0002 | 0/0 | 16 | 0 | 7 | 5 | 0 | 4 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0003 | 0/0 | 16 | 1 | 0 | 15 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0004 | 0/0 | 11 | 5 | 3 | 0 | 2 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0005 | 0/0 | 11 | 0 | 9 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0006 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0008 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0009 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0010 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
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 | 1842 | 173 | 32 | 25 | 89 | 9 | 17 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0002 | 1/0 | 1842 | 122 | 30 | 35 | 32 | 6 | 18 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0004 | 0/0 | 1842 | 19 | 19 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0005 | 0/0 | 1842 | 5 | 4 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0010 | 0/0 | 1842 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0011 | 0/0 | 1842 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0002c0003 | 0/0 | 1842 | 32 | 2 | 16 | 7 | 1 | 6 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0002c0008 | 0/0 | 1842 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0003c0006 | 0/0 | 1842 | 4 | 3 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0004c0007 | 0/0 | 1842 | 4 | 0 | 0 | 4 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0005c0009 | 0/0 | 1842 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0006c0012 | 0/0 | 1842 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3028 | 170 | 31 | 24 | 88 | 9 | 17 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0001t0006 | 0/0 | 3029 | 3 | 1 | 1 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0002t0001 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0002t0002 | 1/0 | 3026 | 110 | 29 | 26 | 31 | 5 | 18 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0002t0003 | 0/0 | 3026 | 6 | 0 | 6 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0002t0004 | 0/0 | 3027 | 5 | 1 | 3 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0004t0001 | 0/0 | 3028 | 9 | 9 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0004t0002 | 0/0 | 3026 | 9 | 9 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0004t0007 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0005t0001 | 0/0 | 3028 | 5 | 4 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0010t0002 | 0/0 | 3026 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0001c0011t0001 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0002c0003t0002 | 0/0 | 3026 | 31 | 2 | 15 | 7 | 1 | 6 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0002c0003t0004 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0002c0008t0002 | 0/0 | 3026 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0003c0006t0005 | 0/0 | 3028 | 4 | 3 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0004c0007t0001 | 0/0 | 3028 | 4 | 0 | 0 | 4 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0005c0009t0002 | 0/0 | 3026 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
a0006c0012t0001 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | copy fasta | chr17 | 47891236 | 47933957 |
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 | 26 | 2 | 1 | 18 | 2 | 3 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0003 | 0/0 | 14 | 1 | 0 | 13 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0009 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0010 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0006g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0002 | 0/0 | 9 | 0 | 1 | 4 | 0 | 4 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0004 | 0/0 | 11 | 5 | 3 | 0 | 2 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0005 | 0/0 | 10 | 0 | 8 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0003g0002 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0002t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0004t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0005t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0010t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0001c0011t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0006 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0003t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0008t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0008t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0002c0008t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0003c0006t0005g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0003c0006t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0004c0007t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0004c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0004c0007t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0005c0009t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
a0006c0012t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0110 | EUR | GBR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0052 | EUR | GBR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0049 | EUR | GBR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0004 | EUR | FIN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00544 | hp2 | a0006 | c0012 | t0001 | g0197 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00558 | hp1 | a0001 | c0005 | t0001 | g0105 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00735 | hp2 | a0002 | c0003 | t0002 | g0083 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00741 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG00741 | hp2 | a0001 | c0002 | t0004 | g0103 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01069 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01070 | hp1 | a0002 | c0003 | t0002 | g0077 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01071 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01099 | hp1 | a0002 | c0003 | t0002 | g0082 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01106 | hp1 | a0003 | c0006 | t0005 | g0164 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01106 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01109 | hp1 | a0002 | c0003 | t0002 | g0023 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01109 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01192 | hp1 | a0001 | c0002 | t0004 | g0075 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01257 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0042 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01346 | hp1 | a0002 | c0003 | t0002 | g0090 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0122 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01358 | hp2 | a0002 | c0003 | t0002 | g0126 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0108 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01433 | hp2 | a0002 | c0003 | t0002 | g0006 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01496 | hp2 | a0002 | c0003 | t0002 | g0087 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01515 | hp1 | a0002 | c0003 | t0002 | g0006 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01934 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0113 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0111 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01975 | hp2 | a0002 | c0003 | t0002 | g0089 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01978 | hp1 | a0002 | c0003 | t0004 | g0088 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02004 | hp1 | a0001 | c0010 | t0002 | g0121 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02027 | hp2 | a0002 | c0003 | t0002 | g0086 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0093 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02074 | hp1 | a0004 | c0007 | t0001 | g0003 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02135 | hp1 | a0004 | c0007 | t0001 | g0130 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02155 | hp1 | a0004 | c0007 | t0001 | g0139 | EAS | CDX | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02257 | hp1 | a0001 | c0005 | t0001 | g0096 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0218 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02273 | hp1 | a0002 | c0003 | t0002 | g0023 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02273 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02293 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02630 | hp1 | a0001 | c0004 | t0002 | g0029 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0098 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02735 | hp1 | a0002 | c0003 | t0002 | g0081 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02818 | hp1 | a0001 | c0004 | t0002 | g0014 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02818 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0220 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02896 | hp2 | a0003 | c0006 | t0005 | g0017 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02965 | hp2 | a0001 | c0004 | t0002 | g0129 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02970 | hp2 | a0001 | c0004 | t0001 | g0217 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02976 | hp2 | a0001 | c0004 | t0001 | g0215 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0070 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03098 | hp2 | a0001 | c0002 | t0004 | g0012 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03130 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03209 | hp1 | a0001 | c0004 | t0001 | g0216 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03209 | hp2 | a0001 | c0004 | t0002 | g0028 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03225 | hp1 | a0001 | c0004 | t0001 | g0221 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03225 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03239 | hp2 | a0002 | c0003 | t0002 | g0080 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03453 | hp2 | a0001 | c0004 | t0002 | g0028 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03486 | hp2 | a0002 | c0003 | t0002 | g0079 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03492 | hp1 | a0002 | c0003 | t0002 | g0125 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03516 | hp1 | a0001 | c0004 | t0002 | g0029 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03540 | hp1 | a0001 | c0004 | t0002 | g0014 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03579 | hp1 | a0003 | c0006 | t0005 | g0017 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03579 | hp2 | a0001 | c0004 | t0002 | g0014 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0097 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03669 | hp2 | a0002 | c0003 | t0002 | g0006 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03688 | hp1 | a0002 | c0003 | t0002 | g0084 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0120 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04228 | hp1 | a0002 | c0003 | t0002 | g0085 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0091 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18522 | hp2 | a0003 | c0006 | t0005 | g0017 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | CHB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18942 | hp2 | a0001 | c0011 | t0001 | g0228 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18943 | hp2 | a0002 | c0003 | t0002 | g0222 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18946 | hp1 | a0002 | c0008 | t0002 | g0199 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18956 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18969 | hp2 | a0002 | c0003 | t0002 | g0117 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18978 | hp1 | a0002 | c0003 | t0002 | g0223 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18995 | hp1 | a0002 | c0008 | t0002 | g0200 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18995 | hp2 | a0004 | c0007 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19000 | hp1 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19005 | hp2 | a0002 | c0003 | t0002 | g0039 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | LWK | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19030 | hp2 | a0001 | c0004 | t0007 | g0127 | AFR | LWK | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19057 | hp2 | a0002 | c0008 | t0002 | g0190 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19082 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA19240 | hp2 | a0002 | c0003 | t0002 | g0078 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | ASW | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ASW | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0101 | EUR | TSI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | GIH | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20905 | hp2 | a0005 | c0009 | t0002 | g0055 | SAS | GIH | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG01123 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0219 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG03471 | hp2 | a0001 | c0004 | t0002 | g0128 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | USA | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | USA | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA18955 | hp2 | a0002 | c0003 | t0002 | g0039 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | USA | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | LWK | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | LWK | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0207 | REF | REF | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0021 | REF | REF | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:47896288
|
T | G | 1 | a0005 | 1 | NA20905.hp2 | start_lost | HIGH | c.2T>G | p.Met1? | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/7 | 53/3026 | 2/1842 | 1/613 | chr17 | 47896288 | ||
chr17:47916750
|
G | T | 1 | a0004 | 4 | HG02074.hp1 HG02135.hp1 HG02155.hp1 others(1): Show |
missense_variant | MODERATE | c.679G>T | p.Ala227Ser | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 730/3026 | 679/1842 | 227/613 | chr17 | 47916750 | ||
chr17:47923040
|
T | C | 1 | a0002 | 35 | HG00735.hp2 HG00741.hp1 HG01069.hp1 others(32): Show |
missense_variant | MODERATE | c.1138T>C | p.Ser380Pro | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/7 | 1189/3026 | 1138/1842 | 380/613 | chr17 | 47923040 | ||
chr17:47923046
|
A | G | 1 | a0003 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.1144A>G | p.Thr382Ala | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/7 | 1195/3026 | 1144/1842 | 382/613 | chr17 | 47923046 | ||
chr17:47925410
|
G | T | 1 | a0006 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.1610G>T | p.Arg537Leu | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/7 | 1661/3026 | 1610/1842 | 537/613 | chr17 | 47925410 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:47916678
|
C | T | 7 | a0001c0001a0001c0004a0001c0011others(4): Show | 205 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(202): Show |
synonymous_variant | LOW | c.607C>T | p.Leu203Leu | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 658/3026 | 607/1842 | 203/613 | chr17 | 47916678 | ||
chr17:47916683
|
A | G | 1 | a0001c0010 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.612A>G | p.Thr204Thr | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 663/3026 | 612/1842 | 204/613 | chr17 | 47916683 | ||
chr17:47916728
|
T | C | 7 | a0001c0001a0001c0004a0001c0011others(4): Show | 205 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(202): Show |
synonymous_variant | LOW | c.657T>C | p.Leu219Leu | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 708/3026 | 657/1842 | 219/613 | chr17 | 47916728 | ||
chr17:47916788
|
G | A | 5 | a0001c0001a0001c0011a0002c0008others(2): Show | 182 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(179): Show |
synonymous_variant | LOW | c.717G>A | p.Pro239Pro | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 768/3026 | 717/1842 | 239/613 | chr17 | 47916788 | ||
chr17:47917106
|
G | A | 1 | a0001c0011 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.1035G>A | p.Gln345Gln | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 1086/3026 | 1035/1842 | 345/613 | chr17 | 47917106 | ||
chr17:47925378
|
G | T | 5 | a0001c0001a0001c0005a0001c0011others(2): Show | 184 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(181): Show |
synonymous_variant | LOW | c.1578G>T | p.Val526Val | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/7 | 1629/3026 | 1578/1842 | 526/613 | chr17 | 47925378 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:47928098
|
G | A | 1 | a0001c0002t0003 | 6 | HG00738.hp1 HG01106.hp2 HG01934.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*274G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 274 | chr17 | 47928098 | |||||
chr17:47928164
|
A | AC | 3 | a0001c0001t0006a0001c0002t0004a0002c0003t0004 | 9 | HG00741.hp2 HG01109.hp2 HG01123.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*346dupC | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 347 | INFO_REALIGN_3_PRIME | chr17 | 47928164 | ||||
chr17:47928426
|
A | ACT | 9 | a0001c0001t0001a0001c0001t0006a0001c0002t0001others(6): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*605_*606dupCT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 607 | INFO_REALIGN_3_PRIME | chr17 | 47928426 | ||||
chr17:47928485
|
T | C | 1 | a0001c0004t0007 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*661T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 661 | chr17 | 47928485 | |||||
chr17:47928602
|
T | C | 1 | a0003c0006t0005 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*778T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 778 | chr17 | 47928602 | |||||
chr17:47928932
|
T | G | 1 | a0001c0004t0007 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1108T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 1108 | chr17 | 47928932 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:47896319
|
G | T | 2 | a0001c0002t0002g0040a0001c0002t0002g0230 | 3 | HG00639.hp1 HG01123.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.7+26G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896319 | ||||||
chr17:47896398
|
G | A | 1 | a0001c0002t0002g0041 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.7+105G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896398 | ||||||
chr17:47896427
|
A | T | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG01175.hp2 HG01192.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+134A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896427 | ||||||
chr17:47896592
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.7+299C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896592 | ||||||
chr17:47896650
|
C | T | 3 | a0002c0003t0002g0039a0002c0003t0002g0222a0002c0003t0002g0223 | 4 | NA18943.hp2 NA18955.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+357C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896650 | ||||||
chr17:47896721
|
G | A | 1 | a0002c0003t0002g0042 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.7+428G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896721 | ||||||
chr17:47896758
|
C | T | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+465C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896758 | ||||||
chr17:47896885
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 105 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.7+592C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896885 | ||||||
chr17:47896886
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.7+593A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896886 | ||||||
chr17:47896919
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 203 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.7+626C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896919 | ||||||
chr17:47897128
|
C | T | 2 | a0002c0003t0002g0125a0002c0003t0002g0126 | 2 | HG01358.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.7+835C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47897128 | ||||||
chr17:47897684
|
G | A | 4 | a0001c0002t0002g0011a0001c0002t0002g0043a0001c0002t0002g0044others(1): Show | 6 | NA18747.hp1 NA18956.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+1391G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47897684 | ||||||
chr17:47897819
|
C | T | 1 | a0001c0002t0002g0124 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.7+1526C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47897819 | ||||||
chr17:47897910
|
C | T | 1 | a0001c0002t0002g0123 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.7+1617C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47897910 | ||||||
chr17:47898026
|
A | T | 1 | a0001c0002t0002g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.7+1733A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898026 | ||||||
chr17:47898157
|
C | T | 1 | a0001c0010t0002g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.7+1864C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898157 | ||||||
chr17:47898167
|
G | T | 1 | a0001c0002t0002g0027 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.7+1874G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898167 | ||||||
chr17:47898209
|
A | T | 1 | a0001c0002t0002g0120 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.7+1916A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898209 | ||||||
chr17:47898333
|
T | G | 1 | a0001c0004t0007g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7+2040T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898333 | ||||||
chr17:47898489
|
T | C | 5 | a0001c0004t0002g0014a0001c0004t0002g0028a0001c0004t0002g0029others(2): Show | 9 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+2196T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898489 | ||||||
chr17:47898623
|
T | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(25): Show | 47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+2330T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898623 | ||||||
chr17:47898792
|
A | G | 2 | a0001c0002t0002g0118a0001c0002t0002g0119 | 2 | NA18950.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.7+2499A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898792 | ||||||
chr17:47899023
|
T | G | 28 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(25): Show | 47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+2730T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899023 | ||||||
chr17:47899105
|
C | G | 1 | a0001c0001t0001g0153 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.7+2812C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899105 | ||||||
chr17:47899199
|
T | C | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+2906T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899199 | ||||||
chr17:47899234
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.7+2941C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899234 | ||||||
chr17:47899257
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.7+2964C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899257 | ||||||
chr17:47899340
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+3047A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899340 | ||||||
chr17:47899372
|
T | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(41): Show | 65 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.7+3079T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899372 | ||||||
chr17:47899458
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 116 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.7+3165A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899458 | ||||||
chr17:47899483
|
A | G | 1 | a0001c0001t0001g0030 | 2 | HG02148.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.7+3190A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899483 | ||||||
chr17:47899526
|
T | C | 1 | a0004c0007t0001g0130 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.7+3233T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899526 | ||||||
chr17:47899722
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0170a0001c0001t0001g0171 | 4 | HG00438.hp2 HG00639.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+3429G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899722 | ||||||
chr17:47899818
|
C | T | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+3525C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899818 | ||||||
chr17:47900136
|
A | T | 15 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0154others(12): Show | 17 | HG02080.hp2 HG02148.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+3843A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900136 | ||||||
chr17:47900259
|
A | G | 1 | a0002c0003t0002g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.7+3966A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900259 | ||||||
chr17:47900266
|
A | G | 15 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0154others(12): Show | 17 | HG02080.hp2 HG02148.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+3973A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900266 | ||||||
chr17:47900326
|
G | T | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+4033G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900326 | ||||||
chr17:47900347
|
C | T | 1 | a0001c0002t0002g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7+4054C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900347 | ||||||
chr17:47900470
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01993.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.7+4177C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900470 | ||||||
chr17:47900500
|
G | A | 3 | a0001c0004t0001g0215a0001c0004t0001g0216a0001c0004t0001g0217 | 3 | HG02970.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.7+4207G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900500 | ||||||
chr17:47900745
|
C | T | 72 | a0001c0002t0001g0110a0001c0002t0002g0002a0001c0002t0002g0005others(69): Show | 109 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.7+4452C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900745 | ||||||
chr17:47901077
|
AGTCAC | A | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+4787_7+4791delCA others(3): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47901077 | |||||
chr17:47901149
|
C | CT | 78 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 128 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.7+4870dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47901149 | |||||
chr17:47901240
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7+4947C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901240 | ||||||
chr17:47901280
|
T | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(25): Show | 47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+4987T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901280 | ||||||
chr17:47901335
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.7+5042C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901335 | ||||||
chr17:47901421
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 116 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.7+5128A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901421 | ||||||
chr17:47901447
|
G | GT | 13 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0155others(10): Show | 15 | HG02080.hp2 HG02148.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.7+5162dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47901447 | |||||
chr17:47901513
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+5220C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901513 | ||||||
chr17:47901869
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.7+5576T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901869 | ||||||
chr17:47902053
|
A | G | 1 | a0001c0002t0002g0114 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7+5760A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47902053 | ||||||
chr17:47902491
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.7+6198G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47902491 | ||||||
chr17:47902894
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+6601T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47902894 | ||||||
chr17:47903036
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.7+6743G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903036 | ||||||
chr17:47903136
|
G | A | 2 | a0001c0002t0002g0046a0001c0002t0002g0047 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.7+6843G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903136 | ||||||
chr17:47903394
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+7101G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903394 | ||||||
chr17:47903527
|
C | T | 5 | a0001c0004t0002g0014a0001c0004t0002g0028a0001c0004t0002g0029others(2): Show | 9 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+7234C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903527 | ||||||
chr17:47903541
|
C | T | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+7248C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903541 | ||||||
chr17:47903590
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7+7297C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903590 | ||||||
chr17:47903638
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 95 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.7+7345A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903638 | ||||||
chr17:47903739
|
A | C | 2 | a0001c0002t0002g0040a0001c0002t0002g0230 | 3 | HG00639.hp1 HG01123.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.7+7446A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903739 | ||||||
chr17:47903912
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 129 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.7+7619T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903912 | ||||||
chr17:47903957
|
T | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(25): Show | 47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+7664T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903957 | ||||||
chr17:47903991
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 129 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.7+7698A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903991 | ||||||
chr17:47904058
|
C | T | 1 | a0001c0002t0002g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7+7765C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904058 | ||||||
chr17:47904144
|
A | C | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+7851A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904144 | ||||||
chr17:47904170
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 203 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.7+7877T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904170 | ||||||
chr17:47904178
|
T | TG | 2 | a0001c0001t0001g0037a0001c0001t0001g0210 | 3 | HG00558.hp2 NA18987.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.7+7887dupG | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904178 | |||||
chr17:47904262
|
C | CA | 74 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(71): Show | 123 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.7+7987dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904262 | |||||
chr17:47904262
|
C | CAA | 8 | a0001c0001t0001g0034a0001c0001t0001g0170a0001c0001t0001g0172others(5): Show | 10 | HG00597.hp1 HG01175.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+7986_7+7987dupAA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904262 | |||||
chr17:47904282
|
A | T | 1 | a0001c0002t0002g0113 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.7+7989A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904282 | ||||||
chr17:47904553
|
G | A | 26 | a0001c0002t0002g0040a0001c0002t0002g0230a0002c0003t0002g0006others(23): Show | 35 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.7+8260G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904553 | ||||||
chr17:47904569
|
T | G | 1 | a0002c0003t0002g0076 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.7+8276T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904569 | ||||||
chr17:47904570
|
G | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02486.hp1 HG02698.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7+8277G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904570 | ||||||
chr17:47904647
|
C | T | 1 | a0001c0002t0002g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7+8354C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904647 | ||||||
chr17:47904648
|
G | A | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+8355G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904648 | ||||||
chr17:47904713
|
G | GT | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 129 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.7+8424dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904713 | |||||
chr17:47904768
|
A | AT | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+8480dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904768 | |||||
chr17:47904812
|
C | G | 1 | a0001c0001t0001g0207 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.7+8519C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904812 | ||||||
chr17:47904881
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7+8588C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904881 | ||||||
chr17:47904893
|
C | T | 2 | a0001c0004t0001g0038a0001c0004t0001g0221 | 3 | HG02818.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7+8600C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904893 | ||||||
chr17:47904953
|
G | A | 2 | a0001c0002t0002g0020a0001c0002t0002g0048 | 3 | HG02109.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7+8660G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904953 | ||||||
chr17:47904980
|
C | G | 72 | a0001c0002t0001g0110a0001c0002t0002g0002a0001c0002t0002g0005others(69): Show | 109 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.7+8687C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904980 | ||||||
chr17:47904994
|
A | T | 9 | a0001c0002t0001g0110a0001c0002t0002g0005a0001c0002t0002g0108others(6): Show | 18 | HG00099.hp1 HG00738.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.7+8701A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904994 | ||||||
chr17:47905071
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7+8778T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905071 | ||||||
chr17:47905107
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(25): Show | 47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+8814C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905107 | ||||||
chr17:47905431
|
G | A | 72 | a0001c0002t0001g0110a0001c0002t0002g0002a0001c0002t0002g0005others(69): Show | 109 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.7+9138G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905431 | ||||||
chr17:47905674
|
A | G | 1 | a0001c0005t0001g0013 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.7+9381A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905674 | ||||||
chr17:47905708
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0166 | 3 | HG01243.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.7+9415C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905708 | ||||||
chr17:47905817
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.8-9495C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905817 | ||||||
chr17:47905911
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.8-9401G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905911 | ||||||
chr17:47906391
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.8-8921C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47906391 | ||||||
chr17:47906529
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.8-8783C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47906529 | ||||||
chr17:47906660
|
C | T | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-8652C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47906660 | ||||||
chr17:47906894
|
C | T | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-8418C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47906894 | ||||||
chr17:47907072
|
T | C | 1 | a0001c0002t0002g0073 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.8-8240T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907072 | ||||||
chr17:47907243
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.8-8069G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907243 | ||||||
chr17:47907555
|
A | G | 13 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0155others(10): Show | 15 | HG02080.hp2 HG02148.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-7757A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907555 | ||||||
chr17:47907583
|
A | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(41): Show | 65 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.8-7729A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907583 | ||||||
chr17:47907699
|
G | A | 1 | a0001c0004t0007g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8-7613G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907699 | ||||||
chr17:47907877
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.8-7435C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907877 | ||||||
chr17:47908048
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 129 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.8-7264A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908048 | ||||||
chr17:47908228
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0166 | 3 | HG01243.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.8-7084A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908228 | ||||||
chr17:47908458
|
C | G | 1 | a0001c0002t0002g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.8-6854C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908458 | ||||||
chr17:47908586
|
C | G | 1 | a0001c0002t0002g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.8-6726C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908586 | ||||||
chr17:47908783
|
G | C | 1 | a0001c0002t0002g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.8-6529G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908783 | ||||||
chr17:47908850
|
C | T | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-6462C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908850 | ||||||
chr17:47908916
|
C | A | 72 | a0001c0002t0001g0110a0001c0002t0002g0002a0001c0002t0002g0005others(69): Show | 109 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.8-6396C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908916 | ||||||
chr17:47908962
|
G | A | 4 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0052others(1): Show | 4 | HG00099.hp2 HG01255.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-6350G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908962 | ||||||
chr17:47908973
|
G | C | 1 | a0001c0002t0002g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8-6339G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908973 | ||||||
chr17:47909092
|
C | G | 3 | a0001c0004t0001g0218a0001c0004t0001g0219a0001c0004t0001g0220 | 3 | HG02258.hp2 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.8-6220C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909092 | ||||||
chr17:47909130
|
A | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0177a0001c0001t0001g0178others(6): Show | 10 | HG01081.hp2 HG01169.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-6182A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909130 | ||||||
chr17:47909498
|
C | T | 3 | a0001c0004t0001g0215a0001c0004t0001g0216a0001c0004t0001g0217 | 3 | HG02970.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.8-5814C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909498 | ||||||
chr17:47909917
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.8-5395G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909917 | ||||||
chr17:47909959
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.8-5353T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909959 | ||||||
chr17:47910008
|
C | T | 7 | a0001c0001t0001g0165a0001c0001t0001g0225a0001c0001t0001g0226others(4): Show | 7 | HG01175.hp2 HG01192.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-5304C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47910008 | ||||||
chr17:47910130
|
C | A | 1 | a0001c0001t0001g0224 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.8-5182C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47910130 | ||||||
chr17:47910240
|
T | C | 1 | a0001c0002t0002g0054 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.8-5072T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47910240 | ||||||
chr17:47910294
|
C | T | 4 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0052others(1): Show | 4 | HG00099.hp2 HG01255.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-5018C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47910294 | ||||||
chr17:47910896
|
A | AGTTACCT others(15): Show |
1 | a0001c0002t0002g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.8-4415_8-4394dupGT others(20): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47910896 | |||||
chr17:47911008
|
TTGAGCCC others(22): Show |
T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4302_8-4274delGA others(27): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47911008 | |||||
chr17:47911038
|
T | A | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4274T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911038 | ||||||
chr17:47911039
|
A | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4273A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911039 | ||||||
chr17:47911044
|
G | A | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4268G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911044 | ||||||
chr17:47911046
|
C | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4266C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911046 | ||||||
chr17:47911050
|
A | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4262A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911050 | ||||||
chr17:47911051
|
C | G | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4261C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911051 | ||||||
chr17:47911052
|
C | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4260C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911052 | ||||||
chr17:47911053
|
C | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4259C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911053 | ||||||
chr17:47911090
|
G | C | 1 | a0002c0003t0002g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.8-4222G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911090 | ||||||
chr17:47911167
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 105 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.8-4145G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911167 | ||||||
chr17:47911182
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0150 | 5 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-4130C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911182 | ||||||
chr17:47911465
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.8-3847A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911465 | ||||||
chr17:47911467
|
C | G | 3 | a0001c0002t0002g0091a0001c0002t0002g0106a0001c0002t0002g0122 | 3 | HG01358.hp1 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.8-3845C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911467 | ||||||
chr17:47911506
|
C | CA | 13 | a0001c0001t0001g0170a0001c0002t0002g0024a0001c0002t0002g0092others(10): Show | 15 | HG00597.hp2 HG00621.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-3790dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47911506 | |||||
chr17:47911549
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.8-3763C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911549 | ||||||
chr17:47911584
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 95 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.8-3728G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911584 | ||||||
chr17:47911659
|
A | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 105 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.8-3653A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911659 | ||||||
chr17:47911680
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 129 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.8-3632T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911680 | ||||||
chr17:47911729
|
C | T | 2 | a0001c0002t0002g0070a0001c0002t0002g0071 | 2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.8-3583C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911729 | ||||||
chr17:47911736
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.8-3576C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911736 | ||||||
chr17:47911804
|
C | CA | 11 | a0001c0001t0001g0134a0001c0001t0001g0166a0001c0001t0001g0183others(8): Show | 12 | HG00639.hp1 HG01123.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-3491dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47911804 | |||||
chr17:47911880
|
C | G | 3 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069 | 3 | HG02486.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.8-3432C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911880 | ||||||
chr17:47911911
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8-3401A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911911 | ||||||
chr17:47911972
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8-3340A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911972 | ||||||
chr17:47912442
|
C | CT | 7 | a0001c0001t0001g0149a0001c0001t0001g0170a0001c0001t0001g0204others(4): Show | 7 | HG01123.hp1 HG02080.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-2853dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47912442 | |||||
chr17:47912442
|
C | CTTTTT | 4 | a0001c0004t0002g0014a0001c0004t0002g0028a0001c0004t0002g0029others(1): Show | 8 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-2857_8-2853dupTT others(3): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47912442 | |||||
chr17:47912442
|
CT | C | 7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0150others(4): Show | 7 | HG01070.hp1 HG01175.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-2853delT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47912442 | |||||
chr17:47912457
|
T | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01256.hp2 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.8-2855T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47912457 | ||||||
chr17:47912513
|
C | T | 1 | a0001c0002t0002g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.8-2799C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47912513 | ||||||
chr17:47912850
|
T | TTTTG | 2 | a0001c0004t0001g0215a0001c0004t0002g0028 | 3 | HG02976.hp2 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.8-2438_8-2435dupGT others(2): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47912850 | |||||
chr17:47913231
|
T | C | 73 | a0001c0002t0001g0110a0001c0002t0002g0002a0001c0002t0002g0005others(70): Show | 110 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.8-2081T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47913231 | ||||||
chr17:47913789
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8-1523T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47913789 | ||||||
chr17:47913874
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(54): Show | 103 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.8-1438C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47913874 | ||||||
chr17:47913887
|
T | C | 1 | a0002c0008t0002g0190 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.8-1425T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47913887 | ||||||
chr17:47914059
|
C | T | 3 | a0001c0004t0001g0218a0001c0004t0001g0219a0001c0004t0001g0220 | 3 | HG02258.hp2 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.8-1253C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47914059 | ||||||
chr17:47914357
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.8-955G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47914357 | ||||||
chr17:47914371
|
C | CA | 10 | a0001c0001t0001g0018a0001c0001t0001g0135a0001c0001t0001g0183others(7): Show | 12 | HG02258.hp2 HG02559.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-926dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47914371 | |||||
chr17:47915011
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.8-301G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47915011 | ||||||
chr17:47915043
|
G | A | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-269G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47915043 | ||||||
chr17:47915214
|
C | CA | 55 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(52): Show | 100 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.8-85dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47915214 | |||||
chr17:47915214
|
C | CAA | 5 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(2): Show | 6 | HG02818.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-86_8-85dupAA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47915214 | |||||
chr17:47915256
|
G | A | 26 | a0001c0002t0002g0040a0001c0002t0002g0230a0002c0003t0002g0006others(23): Show | 35 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.8-56G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47915256 | ||||||
chr17:47915266
|
C | G | 8 | a0002c0003t0002g0023a0002c0003t0002g0042a0002c0003t0002g0076others(5): Show | 9 | HG01109.hp1 HG01261.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-46C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47915266 | ||||||
chr17:47915550
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(42): Show | 66 | HG00140.hp1 HG01167.hp1 HG01167.hp2 others(63): Show |
intron_variant | MODIFIER | c.84+162C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915550 | ||||||
chr17:47915635
|
G | A | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.84+247G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915635 | ||||||
chr17:47915813
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.85-343C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915813 | ||||||
chr17:47915834
|
C | G | 10 | a0001c0002t0002g0020a0001c0002t0002g0048a0001c0004t0001g0038others(7): Show | 12 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.85-322C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915834 | ||||||
chr17:47915870
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.85-286C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915870 | ||||||
chr17:47916101
|
C | T | 6 | a0001c0001t0001g0165a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG01175.hp2 HG01192.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-55C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47916101 | ||||||
chr17:47916117
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.85-39C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47916117 | ||||||
chr17:47917158
|
T | C | 15 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0064others(12): Show | 17 | HG00140.hp1 HG01167.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1059+28T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917158 | ||||||
chr17:47917169
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1059+39G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917169 | ||||||
chr17:47917332
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1059+202T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917332 | ||||||
chr17:47917358
|
A | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(128): Show | 208 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.1059+228A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917358 | ||||||
chr17:47917625
|
GT | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(215): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1059+509delT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47917625 | |||||
chr17:47917625
|
GTT | G | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+508_1059+509d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47917625 | |||||
chr17:47917901
|
G | A | 3 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069 | 3 | HG02486.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1059+771G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917901 | ||||||
chr17:47917939
|
G | A | 1 | a0001c0002t0002g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1059+809G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917939 | ||||||
chr17:47918114
|
GT | G | 7 | a0001c0001t0001g0135a0001c0002t0002g0025a0001c0002t0002g0026others(4): Show | 10 | HG01256.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059+997delT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47918114 | |||||
chr17:47918525
|
C | G | 1 | a0002c0003t0002g0126 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1059+1395C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918525 | ||||||
chr17:47918538
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+1408G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918538 | ||||||
chr17:47918769
|
A | T | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+1639A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918769 | ||||||
chr17:47918898
|
C | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(42): Show | 66 | HG00140.hp1 HG01167.hp1 HG01167.hp2 others(63): Show |
intron_variant | MODIFIER | c.1059+1768C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918898 | ||||||
chr17:47918937
|
G | A | 4 | a0001c0004t0002g0014a0001c0004t0002g0028a0001c0004t0002g0029others(1): Show | 8 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1059+1807G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918937 | ||||||
chr17:47919002
|
T | TAC | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(175): Show | 283 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1059+1884_1059+188 others(6): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919002 | |||||
chr17:47919002
|
TAC | T | 26 | a0001c0002t0002g0040a0001c0002t0002g0230a0002c0003t0002g0006others(23): Show | 35 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1059+1884_1059+188 others(6): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919002 | |||||
chr17:47919028
|
T | TAC | 4 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG01515.hp2 HG01517.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+1912_1059+191 others(6): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919028 | |||||
chr17:47919306
|
A | G | 1 | a0001c0005t0001g0013 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1059+2176A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919306 | ||||||
chr17:47919359
|
A | G | 1 | a0001c0002t0002g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1059+2229A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919359 | ||||||
chr17:47919421
|
A | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0152 | 2 | HG02056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1059+2291A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919421 | ||||||
chr17:47919422
|
A | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(123): Show | 199 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.1059+2292A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919422 | ||||||
chr17:47919608
|
C | T | 1 | a0001c0011t0001g0228 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1059+2478C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919608 | ||||||
chr17:47919666
|
A | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0161 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1059+2536A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919666 | ||||||
chr17:47919710
|
G | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(120): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1059+2580G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919710 | ||||||
chr17:47919825
|
C | CTTTT | 34 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(31): Show | 58 | HG00642.hp1 HG01167.hp1 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.1059+2714_1059+271 others(8): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | |||||
chr17:47919825
|
C | CTTTTT | 18 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0065others(15): Show | 20 | HG00140.hp1 HG01074.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1059+2713_1059+271 others(9): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | |||||
chr17:47919825
|
C | CTTTTTT | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0010others(34): Show | 77 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1059+2712_1059+271 others(10): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | |||||
chr17:47919825
|
C | CTTTTTTT | 16 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0170others(13): Show | 20 | HG01081.hp2 HG01123.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1059+2711_1059+271 others(11): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | |||||
chr17:47919825
|
C | CTTTTTTT others(2): Show |
5 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0219others(2): Show | 6 | HG02559.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+2709_1059+271 others(13): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | |||||
chr17:47919825
|
C | CTTTTTTT others(3): Show |
2 | a0001c0004t0001g0216a0001c0004t0001g0217 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1059+2708_1059+271 others(14): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | |||||
chr17:47919825
|
CTT | C | 25 | a0001c0001t0001g0165a0001c0002t0002g0027a0001c0002t0002g0053others(22): Show | 31 | HG00741.hp2 HG01109.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.1059+2716_1059+271 others(6): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | |||||
chr17:47919825
|
CTTT | C | 87 | a0001c0001t0001g0138a0001c0002t0001g0110a0001c0002t0002g0002others(84): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1059+2715_1059+271 others(7): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | |||||
chr17:47919847
|
T | C | 1 | a0002c0008t0002g0190 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1059+2717T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919847 | ||||||
chr17:47919940
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1059+2810G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919940 | ||||||
chr17:47919993
|
C | T | 1 | a0006c0012t0001g0197 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1059+2863C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919993 | ||||||
chr17:47920141
|
C | T | 1 | a0002c0003t0002g0086 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1060-2821C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920141 | ||||||
chr17:47920209
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0140 | 2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1060-2753G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920209 | ||||||
chr17:47920264
|
C | T | 3 | a0001c0002t0002g0026a0001c0002t0002g0093a0001c0002t0002g0112 | 4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-2698C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920264 | ||||||
chr17:47920290
|
A | AT | 15 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0224others(12): Show | 16 | HG00597.hp2 HG02027.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1060-2656dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47920290 | |||||
chr17:47920452
|
G | A | 2 | a0001c0004t0001g0038a0001c0004t0001g0221 | 3 | HG02818.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1060-2510G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920452 | ||||||
chr17:47920574
|
C | G | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-2388C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920574 | ||||||
chr17:47920582
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1060-2380G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920582 | ||||||
chr17:47920648
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1060-2314T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920648 | ||||||
chr17:47920684
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(111): Show | 182 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.1060-2278G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920684 | ||||||
chr17:47920739
|
T | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1060-2223T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920739 | ||||||
chr17:47920762
|
T | C | 8 | a0001c0004t0001g0038a0001c0004t0001g0215a0001c0004t0001g0216others(5): Show | 9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-2200T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920762 | ||||||
chr17:47921127
|
G | A | 2 | a0001c0002t0002g0097a0001c0002t0002g0098 | 2 | HG02683.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1060-1835G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921127 | ||||||
chr17:47921319
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG00438.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1060-1643A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921319 | ||||||
chr17:47921401
|
A | G | 1 | a0001c0005t0001g0013 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1060-1561A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921401 | ||||||
chr17:47921464
|
C | A | 2 | a0001c0002t0002g0099a0001c0002t0002g0100 | 2 | NA18964.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1060-1498C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921464 | ||||||
chr17:47921674
|
C | A | 1 | a0001c0002t0002g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1060-1288C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921674 | ||||||
chr17:47921754
|
A | G | 46 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(43): Show | 67 | HG00140.hp1 HG01167.hp1 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.1060-1208A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921754 | ||||||
chr17:47922073
|
G | A | 5 | a0001c0004t0002g0014a0001c0004t0002g0028a0001c0004t0002g0029others(2): Show | 9 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-889G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922073 | ||||||
chr17:47922205
|
T | C | 1 | a0001c0004t0002g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1060-757T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922205 | ||||||
chr17:47922216
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1060-746T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922216 | ||||||
chr17:47922257
|
C | T | 1 | a0002c0003t0002g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1060-705C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922257 | ||||||
chr17:47922467
|
G | C | 1 | a0001c0002t0002g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1060-495G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922467 | ||||||
chr17:47922524
|
CTT | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(43): Show | 67 | HG00140.hp1 HG01167.hp1 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.1060-427_1060-426d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47922524 | |||||
chr17:47922713
|
G | A | 1 | a0001c0010t0002g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1060-249G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922713 | ||||||
chr17:47922831
|
G | A | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG01175.hp2 HG01192.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-131G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922831 | ||||||
chr17:47922906
|
G | A | 1 | a0002c0003t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1060-56G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922906 | ||||||
chr17:47923282
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01081.hp2 | splice_region_variant&intron_variant | LOW | c.1372+8T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923282 | ||||||
chr17:47923335
|
C | T | 1 | a0001c0010t0002g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1372+61C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923335 | ||||||
chr17:47923505
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1372+231G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923505 | ||||||
chr17:47923539
|
C | T | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+265C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923539 | ||||||
chr17:47923739
|
C | T | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+465C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923739 | ||||||
chr17:47923862
|
C | T | 1 | a0002c0003t0002g0085 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1372+588C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923862 | ||||||
chr17:47923946
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1372+672C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923946 | ||||||
chr17:47924127
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1373-792T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924127 | ||||||
chr17:47924134
|
G | GT | 15 | a0001c0001t0001g0136a0001c0001t0001g0141a0001c0001t0001g0152others(12): Show | 15 | HG01175.hp2 HG01261.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1373-772dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 47924134 | |||||
chr17:47924169
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(111): Show | 184 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.1373-750G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924169 | ||||||
chr17:47924309
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1373-610A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924309 | ||||||
chr17:47924339
|
A | AT | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(227): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1373-579dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 47924339 | |||||
chr17:47924502
|
C | A | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1373-417C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924502 | ||||||
chr17:47924652
|
C | G | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-267C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924652 | ||||||
chr17:47924798
|
C | G | 2 | a0001c0004t0001g0215a0001c0004t0001g0217 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1373-121C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924798 | ||||||
chr17:47925822
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 197 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.1741+281A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47925822 | ||||||
chr17:47925882
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1741+341A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47925882 | ||||||
chr17:47925904
|
C | CATTTT | 1 | a0003c0006t0005g0017 | 3 | HG02896.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1741+363_1741+364i others(7): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47925904 | ||||||
chr17:47925905
|
C | CT | 38 | a0001c0002t0002g0012a0001c0002t0002g0044a0001c0002t0002g0047others(35): Show | 43 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1741+392dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | |||||
chr17:47925905
|
C | CTT | 5 | a0001c0001t0001g0168a0001c0002t0002g0104a0001c0004t0001g0220others(2): Show | 6 | HG01978.hp1 HG02630.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741+391_1741+392d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | |||||
chr17:47925905
|
C | T | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+364C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47925905 | ||||||
chr17:47925905
|
CT | C | 9 | a0001c0001t0001g0132a0001c0001t0001g0136a0001c0001t0001g0144others(6): Show | 10 | HG02109.hp1 HG02109.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1741+392delT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | |||||
chr17:47925905
|
CTT | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0131others(17): Show | 37 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1741+391_1741+392d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | |||||
chr17:47925905
|
CTTTTTT | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0165a0001c0001t0001g0174others(8): Show | 18 | HG01175.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1741+387_1741+392d others(8): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | |||||
chr17:47925905
|
CTTTTTTT | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(47): Show | 89 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1741+386_1741+392d others(9): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | |||||
chr17:47925905
|
CTTTTTTT others(1): Show |
C | 5 | a0001c0001t0001g0031a0001c0001t0001g0166a0001c0001t0001g0181others(2): Show | 6 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+385_1741+392d others(10): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | |||||
chr17:47925905
|
CTTTTTTT others(4): Show |
C | 17 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0064others(14): Show | 19 | HG00140.hp1 HG01167.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.1741+382_1741+392d others(13): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | |||||
chr17:47926161
|
C | G | 2 | a0003c0006t0005g0017a0003c0006t0005g0164 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+620C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926161 | ||||||
chr17:47926192
|
G | T | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+651G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926192 | ||||||
chr17:47926193
|
A | T | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+652A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926193 | ||||||
chr17:47926194
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+653G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926194 | ||||||
chr17:47926195
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+654G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926195 | ||||||
chr17:47926196
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+655C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926196 | ||||||
chr17:47926315
|
G | GT | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(118): Show | 192 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.1741+789dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47926315 | |||||
chr17:47926315
|
G | GTT | 4 | a0001c0001t0001g0193a0001c0001t0001g0210a0003c0006t0005g0017others(1): Show | 6 | HG01106.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+788_1741+789d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47926315 | |||||
chr17:47926315
|
G | T | 1 | a0001c0004t0007g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1741+774G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926315 | ||||||
chr17:47926334
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0171 | 3 | HG00438.hp2 HG00639.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1741+793A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926334 | ||||||
chr17:47926433
|
C | T | 15 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0064others(12): Show | 17 | HG00140.hp1 HG01167.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1741+892C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926433 | ||||||
chr17:47926440
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1741+899G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926440 | ||||||
chr17:47926493
|
T | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 197 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.1741+952T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926493 | ||||||
chr17:47926523
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 197 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.1741+982C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926523 | ||||||
chr17:47926548
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1741+1007A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926548 | ||||||
chr17:47926744
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0166 | 3 | HG01243.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1742-980C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926744 | ||||||
chr17:47927172
|
A | G | 1 | a0001c0004t0002g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1742-552A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47927172 | ||||||
chr17:47927300
|
A | AAGGTGGG others(16): Show |
1 | a0001c0001t0001g0211 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1742-420_1742-398d others(25): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47927300 | |||||
chr17:47927431
|
G | T | 4 | a0001c0002t0002g0022a0001c0002t0002g0092a0001c0002t0002g0095others(1): Show | 5 | NA18940.hp2 NA18975.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.1742-293G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47927431 | ||||||
chr17:47927462
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1742-262G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47927462 | ||||||
chr17:47927531
|
C | CA | 8 | a0001c0002t0002g0050a0001c0002t0002g0058a0001c0002t0002g0104others(5): Show | 8 | HG00735.hp2 HG01099.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1742-172dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47927531 | |||||
chr17:47927531
|
CA | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0193a0001c0002t0002g0098 | 6 | HG01346.hp2 HG01891.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1742-172delA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47927531 | |||||
chr17:47927531
|
CAA | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(117): Show | 190 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1742-173_1742-172d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47927531 | |||||
chr17:47927644
|
C | A | 1 | a0001c0002t0002g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1742-80C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47927644 |