geneid | 9486 |
---|---|
ensemblid | ENSG00000115526.11 |
hgncid | 19650 |
symbol | CHST10 |
name | carbohydrate sulfotransferase 10 |
refseq_nuc | NM_004854.5 |
refseq_prot | NP_004845.1 |
ensembl_nuc | ENST00000264249.8 |
ensembl_prot | ENSP00000264249.3 |
mane_status | MANE Select |
chr | chr2 |
start | 100391860 |
end | 100417668 |
strand | - |
ver | v1.2 |
region | chr2:100391860-100417668 |
region5000 | chr2:100386860-100422668 |
regionname0 | CHST10_chr2_100391860_100417668 |
regionname5000 | CHST10_chr2_100386860_100422668 |
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 | 356 | 345 | 78 | 69 | 142 | 14 | 40 | 104 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0002 | 0/0 | 356 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0003 | 0/0 | 356 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0004 | 0/0 | 356 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0005 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0006 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0007 | 0/0 | 356 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
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 | 1071 | 188 | 53 | 34 | 76 | 8 | 16 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0002 | 1/0 | 1071 | 123 | 22 | 35 | 37 | 6 | 22 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0003 | 0/0 | 1071 | 11 | 0 | 0 | 11 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0004 | 0/0 | 1071 | 9 | 0 | 0 | 9 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0005 | 0/0 | 1071 | 7 | 7 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0006 | 0/0 | 1071 | 5 | 0 | 0 | 4 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0007 | 0/0 | 1071 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0008 | 0/0 | 1071 | 5 | 5 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0009 | 0/0 | 1071 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0010 | 0/0 | 1071 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0011 | 0/0 | 1071 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0012 | 0/0 | 1071 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0013 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0014 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0015 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
c0016 | 0/0 | 1071 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1784 | 118 | 24 | 33 | 36 | 5 | 19 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0002 | 0/1 | 1784 | 100 | 1 | 20 | 62 | 7 | 9 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0003 | 0/0 | 1784 | 39 | 16 | 10 | 5 | 0 | 8 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0004 | 0/0 | 1784 | 23 | 22 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0005 | 0/0 | 1784 | 21 | 15 | 3 | 3 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0006 | 0/0 | 1784 | 13 | 7 | 0 | 6 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0007 | 0/0 | 1784 | 11 | 0 | 0 | 11 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0008 | 0/0 | 1784 | 9 | 0 | 0 | 9 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0009 | 0/0 | 1784 | 3 | 3 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0010 | 0/0 | 1784 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0011 | 0/0 | 1784 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0012 | 0/0 | 1784 | 2 | 0 | 2 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0013 | 0/0 | 1784 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0014 | 0/0 | 1784 | 2 | 0 | 0 | 0 | 0 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0015 | 0/0 | 1784 | 2 | 0 | 0 | 0 | 1 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0016 | 0/0 | 1784 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0017 | 0/0 | 1784 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0018 | 0/0 | 1784 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0019 | 0/0 | 1784 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0020 | 0/0 | 1784 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0021 | 0/0 | 1784 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0022 | 0/0 | 1784 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0023 | 0/0 | 1784 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0024 | 0/0 | 1784 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0025 | 0/0 | 1784 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0026 | 0/0 | 1784 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0027 | 0/0 | 1784 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0028 | 0/0 | 1784 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
t0029 | 0/0 | 1784 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
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 | 0/1 | 28 | 0 | 6 | 17 | 1 | 3 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0002 | 0/0 | 22 | 0 | 5 | 14 | 1 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0003 | 0/0 | 17 | 5 | 4 | 5 | 0 | 3 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0004 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0005 | 0/0 | 11 | 6 | 0 | 0 | 0 | 5 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0006 | 0/0 | 10 | 0 | 8 | 0 | 2 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0007 | 0/0 | 9 | 0 | 9 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0009 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0013 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0027 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0028 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0030 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
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 | 1071 | 188 | 53 | 34 | 76 | 8 | 16 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0002 | 1/0 | 1071 | 123 | 22 | 35 | 37 | 6 | 22 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0003 | 0/0 | 1071 | 11 | 0 | 0 | 11 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0004 | 0/0 | 1071 | 9 | 0 | 0 | 9 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0006 | 0/0 | 1071 | 5 | 0 | 0 | 4 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0007 | 0/0 | 1071 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0011 | 0/0 | 1071 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0014 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0016 | 0/0 | 1071 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0002c0005 | 0/0 | 1071 | 7 | 7 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0002c0009 | 0/0 | 1071 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0003c0008 | 0/0 | 1071 | 5 | 5 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0004c0010 | 0/0 | 1071 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0005c0013 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0006c0015 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0007c0012 | 0/0 | 1071 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 2854 | 86 | 1 | 20 | 50 | 7 | 7 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0003 | 0/0 | 2854 | 28 | 11 | 9 | 0 | 0 | 8 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0004 | 0/0 | 2854 | 21 | 20 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0005 | 0/0 | 2854 | 18 | 12 | 3 | 3 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0006 | 0/0 | 2854 | 12 | 6 | 0 | 6 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0008 | 0/0 | 2854 | 9 | 0 | 0 | 9 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0011 | 0/0 | 2854 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0012 | 0/0 | 2854 | 2 | 0 | 2 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0013 | 0/0 | 2854 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0016 | 0/0 | 2854 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0017 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0018 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0019 | 0/0 | 2854 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0023 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0024 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0001t0029 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0002t0001 | 1/0 | 2854 | 116 | 22 | 33 | 36 | 5 | 19 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0002t0014 | 0/0 | 2854 | 2 | 0 | 0 | 0 | 0 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0002t0015 | 0/0 | 2854 | 2 | 0 | 0 | 0 | 1 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0002t0020 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0002t0021 | 0/0 | 2854 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0002t0026 | 0/0 | 2854 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0003t0007 | 0/0 | 2854 | 11 | 0 | 0 | 11 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0004t0002 | 0/0 | 2854 | 8 | 0 | 0 | 8 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0004t0025 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0006t0002 | 0/0 | 2854 | 5 | 0 | 0 | 4 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0007t0003 | 0/0 | 2854 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0011t0005 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0011t0006 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0014t0004 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0001c0016t0002 | 0/0 | 2854 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0002c0005t0009 | 0/0 | 2854 | 3 | 3 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0002c0005t0010 | 0/0 | 2854 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0002c0005t0022 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0002c0005t0027 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0002c0009t0001 | 0/0 | 2854 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0003c0008t0003 | 0/0 | 2854 | 5 | 5 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0004c0010t0005 | 0/0 | 2854 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0005c0013t0028 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0006c0015t0004 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
a0007c0012t0003 | 0/0 | 2854 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | copy fasta | chr2 | 100386860 | 100422668 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/1 | 28 | 0 | 6 | 17 | 1 | 3 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0009 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0030 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0003g0005 | 0/0 | 11 | 6 | 0 | 0 | 0 | 5 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0003g0007 | 0/0 | 9 | 0 | 9 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0003g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0003g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0004g0004 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0004g0028 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0006g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0008g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0008g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0011g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0012g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0012g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0013g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0016g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0017g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0018g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0019g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0023g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0024g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0001t0029g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0002 | 0/0 | 22 | 0 | 5 | 14 | 1 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0003 | 0/0 | 17 | 5 | 4 | 5 | 0 | 3 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0006 | 0/0 | 10 | 0 | 8 | 0 | 2 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0027 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0014g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0015g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0020g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0021g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0002t0026g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0003t0007g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0003t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0003t0007g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0004t0002g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0004t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0004t0025g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0006t0002g0013 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0007t0003g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0007t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0011t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0011t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0014t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0001c0016t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0002c0005t0009g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0002c0005t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0002c0005t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0002c0005t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0002c0005t0022g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0002c0005t0027g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0002c0009t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0003c0008t0003g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0003c0008t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0004c0010t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0005c0013t0028g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0006c0015t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
a0007c0012t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0001 | g0104 | EUR | GBR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | FIN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | FIN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00323 | hp1 | a0001 | c0002 | t0015 | g0036 | EUR | FIN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0158 | EUR | FIN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00423 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00438 | hp2 | a0001 | c0001 | t0024 | g0149 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00544 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00544 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00609 | hp2 | a0001 | c0004 | t0002 | g0010 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00621 | hp2 | a0001 | c0006 | t0002 | g0013 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01081 | hp1 | a0001 | c0002 | t0026 | g0110 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0067 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01192 | hp2 | a0001 | c0001 | t0012 | g0128 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01243 | hp1 | a0007 | c0012 | t0003 | g0070 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01261 | hp1 | a0001 | c0001 | t0012 | g0129 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01358 | hp2 | a0001 | c0002 | t0021 | g0054 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0154 | EUR | IBS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0153 | EUR | IBS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0028 | EUR | IBS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0155 | EUR | IBS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01891 | hp2 | a0001 | c0001 | t0029 | g0083 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02015 | hp1 | a0001 | c0001 | t0023 | g0162 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02040 | hp2 | a0001 | c0006 | t0002 | g0013 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02056 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02074 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02083 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02129 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0144 | EAS | CDX | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CDX | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02165 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | CDX | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02257 | hp1 | a0002 | c0005 | t0022 | g0056 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02280 | hp1 | a0003 | c0008 | t0003 | g0071 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02647 | hp2 | a0004 | c0010 | t0005 | g0032 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02698 | hp2 | a0001 | c0002 | t0015 | g0036 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02717 | hp1 | a0002 | c0005 | t0010 | g0055 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0090 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02738 | hp2 | a0001 | c0016 | t0002 | g0150 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02809 | hp2 | a0001 | c0014 | t0004 | g0119 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02895 | hp1 | a0003 | c0008 | t0003 | g0016 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02896 | hp1 | a0002 | c0009 | t0001 | g0042 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02896 | hp2 | a0002 | c0005 | t0009 | g0059 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02897 | hp1 | a0002 | c0009 | t0001 | g0042 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02922 | hp2 | a0002 | c0005 | t0010 | g0057 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02965 | hp1 | a0003 | c0008 | t0003 | g0016 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02970 | hp2 | a0001 | c0011 | t0005 | g0075 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03209 | hp2 | a0003 | c0008 | t0003 | g0016 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03225 | hp1 | a0002 | c0005 | t0009 | g0031 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03453 | hp1 | a0002 | c0005 | t0027 | g0058 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03453 | hp2 | a0003 | c0008 | t0003 | g0016 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0066 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03490 | hp1 | a0001 | c0002 | t0014 | g0038 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03492 | hp1 | a0001 | c0002 | t0014 | g0038 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03540 | hp2 | a0005 | c0013 | t0028 | g0078 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03710 | hp2 | a0001 | c0006 | t0002 | g0013 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG04184 | hp2 | a0001 | c0001 | t0019 | g0052 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | STU | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18522 | hp1 | a0002 | c0005 | t0009 | g0031 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18612 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | CHB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18612 | hp2 | a0001 | c0001 | t0008 | g0124 | EAS | CHB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | CHB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18939 | hp1 | a0001 | c0007 | t0003 | g0017 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18941 | hp1 | a0001 | c0007 | t0003 | g0073 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18944 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18945 | hp2 | a0001 | c0007 | t0003 | g0017 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18951 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18954 | hp1 | a0001 | c0007 | t0003 | g0017 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18957 | hp1 | a0001 | c0003 | t0007 | g0076 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18964 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18965 | hp1 | a0001 | c0001 | t0017 | g0050 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18971 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18972 | hp1 | a0001 | c0001 | t0008 | g0140 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18973 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18973 | hp2 | a0001 | c0001 | t0018 | g0051 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18974 | hp2 | a0001 | c0001 | t0013 | g0049 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18978 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18980 | hp1 | a0001 | c0002 | t0020 | g0053 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18985 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18990 | hp2 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18998 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18999 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19005 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19043 | hp1 | a0001 | c0011 | t0006 | g0077 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19060 | hp1 | a0001 | c0003 | t0007 | g0079 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19060 | hp2 | a0001 | c0004 | t0002 | g0152 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19065 | hp1 | a0001 | c0004 | t0002 | g0137 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19065 | hp2 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19067 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19068 | hp1 | a0001 | c0004 | t0025 | g0165 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19068 | hp2 | a0001 | c0001 | t0011 | g0046 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19078 | hp1 | a0001 | c0001 | t0013 | g0049 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19078 | hp2 | a0001 | c0001 | t0011 | g0046 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19079 | hp2 | a0001 | c0001 | t0008 | g0157 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19084 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19086 | hp2 | a0001 | c0007 | t0003 | g0017 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19088 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19240 | hp1 | a0001 | c0001 | t0016 | g0034 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | ASW | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | ASW | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | TSI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0114 | EUR | TSI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | GIH | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | GIH | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02109 | hp1 | a0001 | c0001 | t0016 | g0034 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02109 | hp2 | a0006 | c0015 | t0004 | g0118 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02559 | hp1 | a0004 | c0010 | t0005 | g0032 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0063 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | USA | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | USA | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | USA | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | USA | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0168 | REF | REF | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:100393298
|
C | T | 1 | a0006 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1018G>A | p.Glu340Lys | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1416/2854 | 1018/1071 | 340/356 | chr2 | 100393298 | ||
chr2:100395526
|
A | T | 1 | a0004 | 2 | HG02559.hp1 HG02647.hp2 |
missense_variant | MODERATE | c.516T>A | p.Asp172Glu | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/7 | 914/2854 | 516/1071 | 172/356 | chr2 | 100395526 | ||
chr2:100395606
|
A | G | 2 | a0002a0005 | 10 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(7): Show |
missense_variant | MODERATE | c.436T>C | p.Ser146Pro | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/7 | 834/2854 | 436/1071 | 146/356 | chr2 | 100395606 | ||
chr2:100402655
|
A | G | 1 | a0005 | 1 | HG03540.hp2 | missense_variant&splice_region_variant | MODERATE | c.101T>C | p.Val34Ala | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/7 | 499/2854 | 101/1071 | 34/356 | chr2 | 100402655 | ||
chr2:100406618
|
C | A | 1 | a0003 | 5 | HG02280.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
missense_variant | MODERATE | c.58G>T | p.Val20Leu | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/7 | 456/2854 | 58/1071 | 20/356 | chr2 | 100406618 | ||
chr2:100406648
|
C | T | 1 | a0007 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.28G>A | p.Ala10Thr | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/7 | 426/2854 | 28/1071 | 10/356 | chr2 | 100406648 | ||
chr2:100417374
|
C | G | 1 | a0002 | 3 | HG02257.hp1 HG02717.hp1 HG02922.hp2 |
splice_region_variant | LOW | c.-104G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | chr2 | 100417374 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:100393272
|
G | A | 1 | a0001c0016 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1044C>T | p.Tyr348Tyr | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1442/2854 | 1044/1071 | 348/356 | chr2 | 100393272 | ||
chr2:100393386
|
C | T | 1 | a0002c0005 | 7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
synonymous_variant | LOW | c.930G>A | p.Pro310Pro | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1328/2854 | 930/1071 | 310/356 | chr2 | 100393386 | ||
chr2:100393446
|
G | A | 1 | a0001c0003 | 11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
synonymous_variant | LOW | c.870C>T | p.Ala290Ala | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1268/2854 | 870/1071 | 290/356 | chr2 | 100393446 | ||
chr2:100393557
|
G | A | 1 | a0001c0007 | 5 | NA18939.hp1 NA18941.hp1 NA18945.hp2 others(2): Show |
synonymous_variant | LOW | c.759C>T | p.Asp253Asp | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1157/2854 | 759/1071 | 253/356 | chr2 | 100393557 | ||
chr2:100393575
|
C | T | 1 | a0001c0014 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.741G>A | p.Pro247Pro | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1139/2854 | 741/1071 | 247/356 | chr2 | 100393575 | ||
chr2:100393581
|
G | A | 1 | a0001c0004 | 9 | HG00609.hp2 NA18973.hp1 NA18978.hp1 others(6): Show |
synonymous_variant | LOW | c.735C>T | p.Gly245Gly | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1133/2854 | 735/1071 | 245/356 | chr2 | 100393581 | ||
chr2:100393620
|
G | C | 12 | a0001c0001a0001c0003a0001c0004others(9): Show | 231 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(228): Show |
synonymous_variant | LOW | c.696C>G | p.Thr232Thr | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1094/2854 | 696/1071 | 232/356 | chr2 | 100393620 | ||
chr2:100395598
|
A | G | 1 | a0001c0006 | 5 | HG00544.hp1 HG00621.hp2 HG02040.hp2 others(2): Show |
synonymous_variant | LOW | c.444T>C | p.Ile148Ile | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/7 | 842/2854 | 444/1071 | 148/356 | chr2 | 100395598 | ||
chr2:100402569
|
G | A | 2 | a0001c0003a0001c0011 | 13 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(10): Show |
synonymous_variant | LOW | c.187C>T | p.Leu63Leu | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/7 | 585/2854 | 187/1071 | 63/356 | chr2 | 100402569 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:100392055
|
T | C | 1 | a0002c0005t0022 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1190 | chr2 | 100392055 | |||||
chr2:100392104
|
G | A | 9 | a0001c0001t0003a0001c0001t0005a0001c0001t0023others(6): Show | 72 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1141C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1141 | chr2 | 100392104 | |||||
chr2:100392105
|
C | A | 9 | a0001c0001t0003a0001c0001t0005a0001c0001t0023others(6): Show | 72 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1140G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1140 | chr2 | 100392105 | |||||
chr2:100392393
|
G | A | 1 | a0001c0002t0015 | 2 | HG00323.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*852C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 852 | chr2 | 100392393 | |||||
chr2:100392432
|
C | T | 4 | a0002c0005t0009a0002c0005t0010a0002c0005t0022others(1): Show | 7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*813G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 813 | chr2 | 100392432 | |||||
chr2:100392487
|
C | T | 1 | a0001c0003t0007 | 11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*758G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 758 | chr2 | 100392487 | |||||
chr2:100392605
|
T | C | 1 | a0001c0001t0019 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 640 | chr2 | 100392605 | |||||
chr2:100392617
|
G | A | 1 | a0002c0005t0009 | 3 | HG02896.hp2 HG03225.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 628 | chr2 | 100392617 | |||||
chr2:100392620
|
C | T | 11 | a0001c0001t0003a0001c0001t0005a0001c0001t0018others(8): Show | 74 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*625G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 625 | chr2 | 100392620 | |||||
chr2:100392709
|
C | T | 1 | a0001c0002t0026 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*536G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 536 | chr2 | 100392709 | |||||
chr2:100392710
|
G | A | 1 | a0001c0001t0024 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*535C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 535 | chr2 | 100392710 | |||||
chr2:100392776
|
C | T | 11 | a0001c0001t0003a0001c0001t0005a0001c0001t0018others(8): Show | 74 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*469G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 469 | chr2 | 100392776 | |||||
chr2:100392860
|
A | G | 1 | a0001c0001t0012 | 2 | HG01192.hp2 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 385 | chr2 | 100392860 | |||||
chr2:100392864
|
T | C | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 232 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*381A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 381 | chr2 | 100392864 | |||||
chr2:100392894
|
C | A | 1 | a0001c0001t0029 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 351 | chr2 | 100392894 | |||||
chr2:100392923
|
C | T | 5 | a0001c0001t0003a0001c0001t0023a0001c0007t0003others(2): Show | 40 | HG00735.hp1 HG00741.hp2 HG01243.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*322G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 322 | chr2 | 100392923 | |||||
chr2:100392927
|
C | T | 1 | a0001c0002t0014 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*318G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 318 | chr2 | 100392927 | |||||
chr2:100393025
|
C | T | 3 | a0001c0001t0004a0001c0014t0004a0006c0015t0004 | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*220G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 220 | chr2 | 100393025 | |||||
chr2:100393026
|
G | T | 3 | a0001c0001t0004a0001c0014t0004a0006c0015t0004 | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*219C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 219 | chr2 | 100393026 | |||||
chr2:100393050
|
G | T | 1 | a0001c0001t0011 | 2 | NA19068.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*195C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 195 | chr2 | 100393050 | |||||
chr2:100393104
|
G | A | 2 | a0001c0001t0016a0001c0001t0029 | 3 | HG01891.hp2 HG02109.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*141C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 141 | chr2 | 100393104 | |||||
chr2:100393133
|
C | T | 3 | a0001c0001t0004a0001c0014t0004a0006c0015t0004 | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*112G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 112 | chr2 | 100393133 | |||||
chr2:100393138
|
G | A | 15 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(12): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*107C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 107 | chr2 | 100393138 | |||||
chr2:100393206
|
A | G | 1 | a0001c0001t0008 | 9 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*39T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 39 | chr2 | 100393206 | |||||
chr2:100415050
|
C | A | 1 | a0001c0001t0013 | 2 | NA18974.hp2 NA19078.hp1 |
5_prime_UTR_variant | MODIFIER | c.-42G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/7 | 8375 | chr2 | 100415050 | |||||
chr2:100415056
|
G | A | 1 | a0001c0004t0025 | 1 | NA19068.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/7 | 8381 | chr2 | 100415056 | |||||
chr2:100415099
|
G | T | 12 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(9): Show | 119 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
5_prime_UTR_variant | MODIFIER | c.-91C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/7 | 8424 | chr2 | 100415099 | |||||
chr2:100417421
|
C | T | 1 | a0001c0002t0021 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-151G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | 10746 | chr2 | 100417421 | |||||
chr2:100417475
|
G | T | 1 | a0001c0002t0020 | 1 | NA18980.hp1 | 5_prime_UTR_variant | MODIFIER | c.-205C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | 10800 | chr2 | 100417475 | |||||
chr2:100417532
|
C | T | 2 | a0001c0001t0018a0001c0001t0019 | 2 | HG04184.hp2 NA18973.hp2 |
5_prime_UTR_variant | MODIFIER | c.-262G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | 10857 | chr2 | 100417532 | |||||
chr2:100417595
|
C | T | 1 | a0001c0001t0017 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-325G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | 10920 | chr2 | 100417595 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:100393897
|
C | T | 7 | a0001c0001t0002g0009a0001c0001t0002g0125a0001c0001t0002g0126others(4): Show | 13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.534-115G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100393897 | ||||||
chr2:100393942
|
A | G | 2 | a0002c0005t0009g0031a0002c0005t0009g0059 | 3 | HG02896.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.534-160T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100393942 | ||||||
chr2:100394208
|
A | G | 3 | a0001c0001t0002g0133a0001c0001t0002g0147a0001c0001t0002g0154 | 3 | HG01515.hp1 HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.534-426T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394208 | ||||||
chr2:100394251
|
CAG | C | 30 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(27): Show | 67 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.534-471_534-470del others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394251 | ||||||
chr2:100394266
|
C | T | 3 | a0001c0001t0005g0062a0001c0001t0005g0063a0001c0001t0005g0065 | 3 | HG02258.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.534-484G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394266 | ||||||
chr2:100394268
|
C | T | 8 | a0001c0001t0004g0004a0001c0001t0004g0028a0001c0001t0004g0040others(5): Show | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.534-486G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394268 | ||||||
chr2:100394306
|
G | A | 1 | a0001c0002t0001g0037 | 2 | NA18993.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.534-524C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394306 | ||||||
chr2:100394398
|
G | A | 67 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(64): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.534-616C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394398 | ||||||
chr2:100394405
|
C | A | 67 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(64): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.534-623G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394405 | ||||||
chr2:100394406
|
G | A | 7 | a0001c0002t0001g0117a0002c0005t0009g0031a0002c0005t0009g0059others(4): Show | 9 | HG02257.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-624C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394406 | ||||||
chr2:100394479
|
T | G | 3 | a0001c0001t0005g0015a0001c0001t0005g0064a0004c0010t0005g0032 | 7 | HG01261.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.534-697A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394479 | ||||||
chr2:100394560
|
C | T | 1 | a0001c0001t0003g0007 | 9 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.534-778G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394560 | ||||||
chr2:100394624
|
C | T | 1 | a0002c0005t0027g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.534-842G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394624 | ||||||
chr2:100394726
|
C | CT | 31 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(28): Show | 68 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(65): Show |
intron_variant | MODIFIER | c.533+782dupA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394726 | ||||||
chr2:100394726
|
CT | C | 62 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(59): Show | 126 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.533+782delA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394726 | ||||||
chr2:100394746
|
C | T | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+763G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394746 | ||||||
chr2:100394779
|
G | A | 116 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(113): Show | 245 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.533+730C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394779 | ||||||
chr2:100394790
|
C | G | 34 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(31): Show | 79 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.533+719G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394790 | ||||||
chr2:100394819
|
G | T | 1 | a0001c0002t0001g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.533+690C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394819 | ||||||
chr2:100394889
|
AT | A | 66 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(63): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.533+619delA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394889 | ||||||
chr2:100395062
|
C | T | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.533+447G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395062 | ||||||
chr2:100395087
|
C | T | 2 | a0001c0001t0005g0021a0001c0001t0005g0068 | 4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+422G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395087 | ||||||
chr2:100395156
|
A | G | 38 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(35): Show | 84 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.533+353T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395156 | ||||||
chr2:100395262
|
C | T | 116 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(113): Show | 245 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.533+247G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395262 | ||||||
chr2:100395415
|
T | C | 67 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(64): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.533+94A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395415 | ||||||
chr2:100395478
|
C | A | 1 | a0001c0001t0003g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.533+31G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395478 | ||||||
chr2:100395487
|
C | A | 4 | a0001c0001t0003g0023a0001c0001t0003g0072a0001c0001t0003g0074others(1): Show | 6 | HG01243.hp1 HG02647.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.533+22G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395487 | ||||||
chr2:100395658
|
C | T | 1 | a0001c0001t0002g0146 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.428-44G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395658 | ||||||
chr2:100395717
|
C | T | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.428-103G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395717 | ||||||
chr2:100395740
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.428-126G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395740 | ||||||
chr2:100395839
|
C | T | 2 | a0001c0001t0005g0021a0001c0001t0005g0068 | 4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-225G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395839 | ||||||
chr2:100395865
|
G | A | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.428-251C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395865 | ||||||
chr2:100396051
|
C | T | 6 | a0001c0002t0021g0054a0002c0005t0009g0031a0002c0005t0009g0059others(3): Show | 7 | HG01358.hp2 HG02257.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-437G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396051 | ||||||
chr2:100396077
|
T | C | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.428-463A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396077 | ||||||
chr2:100396246
|
G | GT | 6 | a0002c0005t0009g0031a0002c0005t0009g0059a0002c0005t0010g0055others(3): Show | 7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-633dupA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396246 | ||||||
chr2:100396324
|
A | C | 1 | a0001c0002t0001g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.428-710T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396324 | ||||||
chr2:100396332
|
C | G | 1 | a0001c0001t0002g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.428-718G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396332 | ||||||
chr2:100396406
|
G | C | 1 | a0001c0001t0002g0151 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.428-792C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396406 | ||||||
chr2:100396471
|
T | A | 1 | a0001c0011t0006g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.428-857A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396471 | ||||||
chr2:100396595
|
T | A | 2 | a0001c0002t0001g0019a0001c0002t0001g0101 | 5 | HG02300.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-981A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396595 | ||||||
chr2:100396622
|
G | A | 3 | a0001c0002t0001g0006a0001c0002t0001g0088a0001c0002t0001g0104 | 12 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.428-1008C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396622 | ||||||
chr2:100396631
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428-1017C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396631 | ||||||
chr2:100396924
|
A | G | 3 | a0001c0001t0008g0124a0001c0001t0008g0144a0001c0001t0008g0157 | 3 | HG02155.hp1 NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.427+984T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396924 | ||||||
chr2:100396958
|
T | A | 3 | a0001c0001t0005g0015a0001c0001t0005g0064a0004c0010t0005g0032 | 7 | HG01261.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+950A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396958 | ||||||
chr2:100396962
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+946A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396962 | ||||||
chr2:100396970
|
C | G | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.427+938G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396970 | ||||||
chr2:100397041
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0043a0001c0001t0002g0123 | 7 | HG00597.hp1 NA18945.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+867G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397041 | ||||||
chr2:100397187
|
A | G | 67 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(64): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.427+721T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397187 | ||||||
chr2:100397198
|
C | T | 3 | a0001c0001t0005g0015a0001c0001t0005g0064a0004c0010t0005g0032 | 7 | HG01261.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+710G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397198 | ||||||
chr2:100397213
|
T | C | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.427+695A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397213 | ||||||
chr2:100397280
|
G | T | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.427+628C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397280 | ||||||
chr2:100397433
|
C | T | 2 | a0001c0001t0006g0033a0001c0001t0006g0081 | 3 | HG02257.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.427+475G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397433 | ||||||
chr2:100397540
|
C | T | 1 | a0001c0001t0004g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.427+368G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397540 | ||||||
chr2:100397582
|
T | C | 2 | a0001c0002t0001g0111a0002c0009t0001g0042 | 3 | HG02896.hp1 HG02897.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.427+326A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397582 | ||||||
chr2:100397734
|
A | C | 2 | a0002c0005t0009g0031a0002c0005t0009g0059 | 3 | HG02896.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.427+174T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397734 | ||||||
chr2:100397759
|
A | G | 6 | a0002c0005t0009g0031a0002c0005t0009g0059a0002c0005t0010g0055others(3): Show | 7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+149T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397759 | ||||||
chr2:100397785
|
C | A | 115 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(112): Show | 243 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.427+123G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397785 | ||||||
chr2:100397829
|
T | A | 1 | a0001c0002t0001g0106 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.427+79A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397829 | ||||||
chr2:100397901
|
C | T | 59 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(56): Show | 122 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
splice_region_variant&intron_variant | LOW | c.427+7G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397901 | ||||||
chr2:100398162
|
G | A | 2 | a0001c0002t0001g0018a0001c0002t0001g0092 | 5 | HG00642.hp1 HG01496.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-20C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398162 | ||||||
chr2:100398276
|
T | C | 1 | a0001c0002t0001g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.193-134A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398276 | ||||||
chr2:100398339
|
G | A | 3 | a0001c0003t0007g0008a0001c0003t0007g0076a0001c0003t0007g0079 | 11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-197C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398339 | ||||||
chr2:100398342
|
C | T | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.193-200G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398342 | ||||||
chr2:100398386
|
A | ATG | 39 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(36): Show | 85 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.193-245_193-244ins others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398386 | ||||||
chr2:100398548
|
A | G | 1 | a0001c0002t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.193-406T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398548 | ||||||
chr2:100398594
|
C | T | 6 | a0002c0005t0009g0031a0002c0005t0009g0059a0002c0005t0010g0055others(3): Show | 7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-452G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398594 | ||||||
chr2:100398607
|
G | A | 6 | a0002c0005t0009g0031a0002c0005t0009g0059a0002c0005t0010g0055others(3): Show | 7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-465C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398607 | ||||||
chr2:100398664
|
T | C | 2 | a0002c0009t0001g0042a0005c0013t0028g0078 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.193-522A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398664 | ||||||
chr2:100398688
|
G | C | 4 | a0001c0002t0001g0019a0001c0002t0001g0100a0001c0002t0001g0101others(1): Show | 7 | HG01884.hp2 HG02300.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-546C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398688 | ||||||
chr2:100398935
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.193-793G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398935 | ||||||
chr2:100398955
|
G | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-813C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398955 | ||||||
chr2:100399102
|
CT | C | 72 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(69): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.193-961delA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399102 | ||||||
chr2:100399102
|
CTT | C | 6 | a0001c0001t0002g0138a0001c0001t0002g0153a0001c0001t0006g0096others(3): Show | 6 | HG01257.hp2 HG01515.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-962_193-961del others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399102 | ||||||
chr2:100399103
|
T | TC | 3 | a0001c0003t0007g0008a0001c0003t0007g0076a0001c0003t0007g0079 | 11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-962_193-961ins others(1): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399103 | ||||||
chr2:100399106
|
T | C | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.193-964A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399106 | ||||||
chr2:100399113
|
T | G | 24 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(21): Show | 60 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.193-971A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399113 | ||||||
chr2:100399139
|
T | C | 67 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(64): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.193-997A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399139 | ||||||
chr2:100399166
|
C | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-1024G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399166 | ||||||
chr2:100399398
|
C | T | 3 | a0001c0003t0007g0008a0001c0003t0007g0076a0001c0003t0007g0079 | 11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-1256G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399398 | ||||||
chr2:100399580
|
G | A | 5 | a0001c0001t0018g0051a0001c0001t0019g0052a0001c0003t0007g0008others(2): Show | 13 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.193-1438C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399580 | ||||||
chr2:100399591
|
A | G | 1 | a0001c0002t0001g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.193-1449T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399591 | ||||||
chr2:100399846
|
C | T | 1 | a0001c0002t0001g0060 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.193-1704G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399846 | ||||||
chr2:100399948
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.193-1806G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399948 | ||||||
chr2:100399979
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.193-1837C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399979 | ||||||
chr2:100400093
|
G | A | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.193-1951C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400093 | ||||||
chr2:100400208
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.193-2066T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400208 | ||||||
chr2:100400214
|
C | T | 1 | a0001c0002t0001g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.193-2072G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400214 | ||||||
chr2:100400267
|
TCTTGTTC others(5): Show |
T | 1 | a0001c0001t0002g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.193-2137_193-2126d others(14): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400267 | ||||||
chr2:100400438
|
G | C | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.192+2126C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400438 | ||||||
chr2:100400569
|
T | C | 1 | a0001c0001t0017g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.192+1995A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400569 | ||||||
chr2:100400673
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.192+1891A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400673 | ||||||
chr2:100400803
|
C | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0134a0001c0001t0011g0046 | 6 | HG00423.hp2 HG02155.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+1761G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400803 | ||||||
chr2:100400883
|
G | A | 8 | a0001c0001t0004g0004a0001c0001t0004g0028a0001c0001t0004g0040others(5): Show | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+1681C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400883 | ||||||
chr2:100400909
|
G | C | 4 | a0001c0002t0001g0105a0001c0002t0001g0112a0001c0002t0001g0114others(1): Show | 5 | HG00738.hp2 HG02683.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+1655C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400909 | ||||||
chr2:100400974
|
C | T | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.192+1590G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400974 | ||||||
chr2:100401081
|
T | C | 5 | a0001c0003t0007g0008a0001c0003t0007g0076a0001c0003t0007g0079others(2): Show | 13 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+1483A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401081 | ||||||
chr2:100401296
|
C | T | 36 | a0001c0001t0002g0045a0001c0001t0003g0005a0001c0001t0003g0007others(33): Show | 82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.192+1268G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401296 | ||||||
chr2:100401434
|
C | T | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.192+1130G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401434 | ||||||
chr2:100401435
|
G | A | 3 | a0001c0001t0005g0015a0001c0001t0005g0064a0004c0010t0005g0032 | 7 | HG01261.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+1129C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401435 | ||||||
chr2:100401448
|
C | T | 4 | a0001c0001t0005g0022a0001c0001t0005g0061a0001c0001t0005g0066others(1): Show | 6 | HG01167.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+1116G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401448 | ||||||
chr2:100401668
|
A | G | 4 | a0001c0002t0001g0025a0001c0002t0001g0084a0002c0009t0001g0042others(1): Show | 7 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+896T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401668 | ||||||
chr2:100401677
|
A | C | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.192+887T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401677 | ||||||
chr2:100401719
|
A | G | 1 | a0001c0002t0001g0107 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.192+845T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401719 | ||||||
chr2:100401751
|
C | A | 1 | a0001c0001t0002g0153 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.192+813G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401751 | ||||||
chr2:100401754
|
T | A | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.192+810A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401754 | ||||||
chr2:100401881
|
C | T | 8 | a0001c0001t0004g0004a0001c0001t0004g0028a0001c0001t0004g0040others(5): Show | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+683G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401881 | ||||||
chr2:100401882
|
G | A | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.192+682C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401882 | ||||||
chr2:100401949
|
C | G | 41 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(38): Show | 89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.192+615G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401949 | ||||||
chr2:100401983
|
C | T | 35 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(32): Show | 80 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.192+581G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401983 | ||||||
chr2:100402160
|
A | G | 8 | a0001c0001t0004g0004a0001c0001t0004g0028a0001c0001t0004g0040others(5): Show | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+404T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100402160 | ||||||
chr2:100402251
|
T | A | 1 | a0001c0001t0003g0024 | 3 | HG03491.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.192+313A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100402251 | ||||||
chr2:100402460
|
C | T | 1 | a0001c0001t0006g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192+104G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100402460 | ||||||
chr2:100402466
|
C | T | 1 | a0001c0001t0008g0140 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.192+98G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100402466 | ||||||
chr2:100402756
|
C | T | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.101-101G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100402756 | ||||||
chr2:100402762
|
C | T | 1 | a0001c0002t0001g0035 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.101-107G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100402762 | ||||||
chr2:100402775
|
C | T | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-120G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100402775 | ||||||
chr2:100402941
|
T | C | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.101-286A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100402941 | ||||||
chr2:100403201
|
G | A | 128 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(125): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.101-546C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403201 | ||||||
chr2:100403345
|
C | T | 7 | a0001c0001t0005g0022a0001c0001t0005g0061a0001c0001t0005g0062others(4): Show | 9 | HG01167.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-690G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403345 | ||||||
chr2:100403347
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.101-692A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403347 | ||||||
chr2:100403453
|
C | T | 1 | a0001c0001t0005g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101-798G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403453 | ||||||
chr2:100403466
|
T | C | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.101-811A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403466 | ||||||
chr2:100403572
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.101-917C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403572 | ||||||
chr2:100403618
|
T | C | 6 | a0002c0005t0009g0031a0002c0005t0009g0059a0002c0005t0010g0055others(3): Show | 7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-963A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403618 | ||||||
chr2:100403674
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.101-1019G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403674 | ||||||
chr2:100403675
|
G | A | 37 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(34): Show | 82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.101-1020C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403675 | ||||||
chr2:100403775
|
C | T | 5 | a0001c0001t0002g0009a0001c0001t0002g0125a0001c0001t0002g0126others(2): Show | 11 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-1120G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403775 | ||||||
chr2:100403777
|
A | G | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.101-1122T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403777 | ||||||
chr2:100403818
|
T | G | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.101-1163A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403818 | ||||||
chr2:100403843
|
G | A | 168 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(165): Show | 362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.101-1188C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403843 | ||||||
chr2:100403970
|
G | C | 4 | a0001c0002t0001g0025a0001c0002t0001g0084a0002c0009t0001g0042others(1): Show | 7 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-1315C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403970 | ||||||
chr2:100404098
|
G | C | 2 | a0001c0001t0016g0034a0001c0001t0029g0083 | 3 | HG01891.hp2 HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.101-1443C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404098 | ||||||
chr2:100404162
|
G | A | 31 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(28): Show | 75 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.101-1507C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404162 | ||||||
chr2:100404168
|
G | A | 2 | a0001c0001t0005g0021a0001c0001t0005g0068 | 4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1513C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404168 | ||||||
chr2:100404256
|
G | A | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.101-1601C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404256 | ||||||
chr2:100404382
|
C | T | 2 | a0001c0002t0001g0027a0001c0002t0001g0106 | 4 | HG01099.hp1 HG01175.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-1727G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404382 | ||||||
chr2:100404436
|
G | A | 35 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(32): Show | 80 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.101-1781C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404436 | ||||||
chr2:100404583
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-1928A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404583 | ||||||
chr2:100404628
|
A | G | 116 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(113): Show | 245 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.100+1948T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404628 | ||||||
chr2:100404673
|
C | T | 37 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(34): Show | 82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+1903G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404673 | ||||||
chr2:100404704
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.100+1872T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404704 | ||||||
chr2:100404933
|
G | A | 1 | a0001c0002t0001g0113 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.100+1643C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404933 | ||||||
chr2:100405155
|
C | A | 1 | a0001c0001t0006g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+1421G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405155 | ||||||
chr2:100405172
|
G | C | 1 | a0001c0001t0002g0048 | 2 | NA18997.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.100+1404C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405172 | ||||||
chr2:100405305
|
G | C | 1 | a0001c0001t0002g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.100+1271C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405305 | ||||||
chr2:100405355
|
C | G | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.100+1221G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405355 | ||||||
chr2:100405537
|
C | G | 4 | a0001c0002t0001g0025a0001c0002t0001g0084a0002c0009t0001g0042others(1): Show | 7 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+1039G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405537 | ||||||
chr2:100405552
|
A | G | 41 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(38): Show | 89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100+1024T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405552 | ||||||
chr2:100405663
|
A | G | 6 | a0001c0001t0006g0033a0001c0001t0006g0080a0001c0001t0006g0081others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+913T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405663 | ||||||
chr2:100405702
|
T | A | 8 | a0001c0001t0004g0004a0001c0001t0004g0028a0001c0001t0004g0040others(5): Show | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.100+874A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405702 | ||||||
chr2:100405807
|
T | C | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100+769A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405807 | ||||||
chr2:100405809
|
G | C | 1 | a0001c0001t0008g0157 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.100+767C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405809 | ||||||
chr2:100405810
|
C | T | 24 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(21): Show | 60 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.100+766G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405810 | ||||||
chr2:100405826
|
A | G | 1 | a0001c0014t0004g0119 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100+750T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405826 | ||||||
chr2:100405887
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.100+689T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405887 | ||||||
chr2:100405948
|
G | T | 37 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(34): Show | 82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+628C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405948 | ||||||
chr2:100406037
|
G | A | 8 | a0001c0001t0004g0004a0001c0001t0004g0028a0001c0001t0004g0040others(5): Show | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.100+539C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406037 | ||||||
chr2:100406047
|
C | T | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.100+529G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406047 | ||||||
chr2:100406177
|
G | A | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100+399C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406177 | ||||||
chr2:100406233
|
T | C | 3 | a0001c0003t0007g0008a0001c0003t0007g0076a0001c0003t0007g0079 | 11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+343A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406233 | ||||||
chr2:100406264
|
G | A | 67 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(64): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.100+312C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406264 | ||||||
chr2:100406272
|
T | C | 1 | a0001c0002t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.100+304A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406272 | ||||||
chr2:100406319
|
C | T | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.100+257G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406319 | ||||||
chr2:100406424
|
C | T | 67 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(64): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.100+152G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406424 | ||||||
chr2:100406483
|
C | G | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.100+93G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406483 | ||||||
chr2:100406501
|
A | G | 41 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(38): Show | 89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100+75T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406501 | ||||||
chr2:100406799
|
T | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0043a0001c0001t0002g0123 | 7 | HG00597.hp1 NA18945.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-92A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100406799 | ||||||
chr2:100406867
|
C | T | 37 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(34): Show | 82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-160G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100406867 | ||||||
chr2:100407060
|
T | C | 1 | a0001c0002t0001g0115 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-32-353A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407060 | ||||||
chr2:100407091
|
G | T | 1 | a0001c0004t0002g0137 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-32-384C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407091 | ||||||
chr2:100407104
|
G | A | 1 | a0001c0002t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-32-397C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407104 | ||||||
chr2:100407114
|
A | G | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-407T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407114 | ||||||
chr2:100407173
|
G | A | 67 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(64): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.-32-466C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407173 | ||||||
chr2:100407237
|
C | T | 37 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(34): Show | 82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-530G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407237 | ||||||
chr2:100407605
|
G | C | 1 | a0001c0001t0002g0158 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-32-898C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407605 | ||||||
chr2:100407691
|
C | T | 1 | a0001c0001t0004g0040 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-32-984G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407691 | ||||||
chr2:100407717
|
A | T | 1 | a0001c0001t0002g0136 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-32-1010T>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407717 | ||||||
chr2:100407743
|
G | A | 6 | a0002c0005t0009g0031a0002c0005t0009g0059a0002c0005t0010g0055others(3): Show | 7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-1036C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407743 | ||||||
chr2:100407848
|
G | A | 1 | a0001c0002t0001g0089 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-32-1141C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407848 | ||||||
chr2:100407922
|
C | A | 3 | a0001c0001t0005g0061a0001c0001t0005g0066a0001c0001t0005g0067 | 3 | HG01167.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-32-1215G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407922 | ||||||
chr2:100407951
|
C | T | 37 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(34): Show | 82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-1244G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407951 | ||||||
chr2:100407976
|
C | T | 5 | a0001c0003t0007g0008a0001c0003t0007g0076a0001c0003t0007g0079others(2): Show | 13 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-32-1269G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407976 | ||||||
chr2:100408010
|
C | G | 1 | a0001c0001t0005g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-32-1303G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408010 | ||||||
chr2:100408130
|
TTAGTA | T | 37 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(34): Show | 82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-1428_-32-1424d others(7): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408130 | ||||||
chr2:100408170
|
T | TA | 10 | a0001c0002t0001g0025a0001c0002t0001g0084a0001c0003t0007g0008others(7): Show | 21 | HG00423.hp1 HG00544.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-32-1464dupT | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408170 | ||||||
chr2:100408226
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-32-1519C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408226 | ||||||
chr2:100408261
|
A | AG | 37 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(34): Show | 82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-1555dupC | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408261 | ||||||
chr2:100408273
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(65): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.-32-1566T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408273 | ||||||
chr2:100408321
|
C | A | 1 | a0001c0001t0012g0129 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-32-1614G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408321 | ||||||
chr2:100408476
|
C | G | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-1769G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408476 | ||||||
chr2:100408650
|
G | A | 2 | a0002c0005t0009g0031a0002c0005t0009g0059 | 3 | HG02896.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-32-1943C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408650 | ||||||
chr2:100408884
|
C | A | 2 | a0001c0001t0004g0004a0001c0001t0004g0121 | 13 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-2177G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408884 | ||||||
chr2:100408927
|
G | C | 24 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(21): Show | 60 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-32-2220C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408927 | ||||||
chr2:100408943
|
C | T | 1 | a0001c0001t0004g0028 | 3 | HG01516.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-32-2236G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408943 | ||||||
chr2:100409073
|
G | C | 41 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(38): Show | 89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.-32-2366C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409073 | ||||||
chr2:100409081
|
G | A | 3 | a0001c0001t0018g0051a0001c0001t0019g0052a0001c0002t0001g0104 | 3 | HG00140.hp1 HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-2374C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409081 | ||||||
chr2:100409104
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-32-2397C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409104 | ||||||
chr2:100409106
|
G | A | 20 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(17): Show | 48 | HG00609.hp1 HG00735.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-32-2399C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409106 | ||||||
chr2:100409201
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-32-2494A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409201 | ||||||
chr2:100409349
|
T | C | 41 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(38): Show | 89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.-32-2642A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409349 | ||||||
chr2:100409483
|
G | A | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-2776C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409483 | ||||||
chr2:100409590
|
C | T | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-2883G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409590 | ||||||
chr2:100409608
|
C | T | 2 | a0002c0009t0001g0042a0005c0013t0028g0078 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-32-2901G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409608 | ||||||
chr2:100409862
|
A | C | 1 | a0001c0002t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-32-3155T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409862 | ||||||
chr2:100409986
|
G | A | 1 | a0001c0011t0006g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-32-3279C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409986 | ||||||
chr2:100409986
|
G | T | 1 | a0001c0001t0002g0135 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-32-3279C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409986 | ||||||
chr2:100410010
|
G | A | 5 | a0001c0001t0004g0004a0001c0001t0004g0041a0001c0001t0004g0120others(2): Show | 17 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32-3303C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410010 | ||||||
chr2:100410179
|
G | A | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-3472C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410179 | ||||||
chr2:100410286
|
T | C | 1 | a0001c0002t0001g0039 | 2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-32-3579A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410286 | ||||||
chr2:100410391
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-32-3684C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410391 | ||||||
chr2:100410659
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-32-3952A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410659 | ||||||
chr2:100410754
|
T | C | 1 | a0001c0003t0007g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-32-4047A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410754 | ||||||
chr2:100410765
|
A | G | 1 | a0001c0002t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-32-4058T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410765 | ||||||
chr2:100410818
|
G | A | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-4111C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410818 | ||||||
chr2:100410938
|
G | A | 38 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(35): Show | 83 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.-33+4103C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410938 | ||||||
chr2:100411116
|
C | CT | 14 | a0001c0001t0002g0044a0001c0001t0002g0127a0001c0001t0002g0134others(11): Show | 27 | HG01884.hp1 HG01928.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-33+3924dupA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411116 | ||||||
chr2:100411116
|
C | CTT | 3 | a0001c0001t0004g0028a0001c0001t0004g0040a0006c0015t0004g0118 | 6 | HG01516.hp1 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+3923_-33+3924d others(4): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411116 | ||||||
chr2:100411116
|
CT | C | 26 | a0001c0001t0002g0132a0001c0001t0003g0005a0001c0001t0003g0007others(23): Show | 68 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.-33+3924delA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411116 | ||||||
chr2:100411116
|
CTT | C | 4 | a0001c0001t0005g0021a0001c0001t0005g0068a0001c0007t0003g0073others(1): Show | 6 | HG02148.hp2 NA18941.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+3923_-33+3924d others(4): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411116 | ||||||
chr2:100411121
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+3920A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411121 | ||||||
chr2:100411247
|
G | A | 1 | a0001c0001t0002g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-33+3794C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411247 | ||||||
chr2:100411263
|
C | T | 8 | a0001c0001t0004g0004a0001c0001t0004g0028a0001c0001t0004g0040others(5): Show | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-33+3778G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411263 | ||||||
chr2:100411295
|
A | G | 1 | a0001c0001t0017g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-33+3746T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411295 | ||||||
chr2:100411366
|
A | C | 42 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(39): Show | 90 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.-33+3675T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411366 | ||||||
chr2:100411600
|
C | T | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+3441G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411600 | ||||||
chr2:100411774
|
G | T | 38 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(35): Show | 83 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.-33+3267C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411774 | ||||||
chr2:100411818
|
C | T | 1 | a0001c0002t0001g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-33+3223G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411818 | ||||||
chr2:100411845
|
G | C | 2 | a0001c0001t0018g0051a0001c0001t0019g0052 | 2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-33+3196C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411845 | ||||||
chr2:100411909
|
G | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0123 | 3 | NA18970.hp2 NA19001.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-33+3132C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411909 | ||||||
chr2:100411997
|
G | C | 3 | a0001c0001t0005g0062a0001c0001t0005g0063a0001c0001t0005g0065 | 3 | HG02258.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+3044C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411997 | ||||||
chr2:100412259
|
G | T | 1 | a0001c0001t0002g0133 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-33+2782C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412259 | ||||||
chr2:100412262
|
G | A | 1 | a0003c0008t0003g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-33+2779C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412262 | ||||||
chr2:100412291
|
G | A | 1 | a0001c0001t0003g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-33+2750C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412291 | ||||||
chr2:100412329
|
T | A | 3 | a0001c0001t0005g0062a0001c0001t0005g0063a0001c0001t0005g0065 | 3 | HG02258.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+2712A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412329 | ||||||
chr2:100412331
|
C | T | 6 | a0001c0001t0006g0033a0001c0001t0006g0080a0001c0001t0006g0081others(3): Show | 8 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+2710G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412331 | ||||||
chr2:100412376
|
G | T | 1 | a0001c0001t0002g0132 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-33+2665C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412376 | ||||||
chr2:100412456
|
G | A | 38 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(35): Show | 83 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.-33+2585C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412456 | ||||||
chr2:100412460
|
TAC | T | 8 | a0001c0001t0004g0004a0001c0001t0004g0028a0001c0001t0004g0040others(5): Show | 23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-33+2579_-33+2580d others(4): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412460 | ||||||
chr2:100412540
|
G | A | 115 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(112): Show | 240 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.-33+2501C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412540 | ||||||
chr2:100412568
|
C | T | 2 | a0001c0002t0001g0011a0001c0002t0001g0089 | 6 | NA18951.hp2 NA18960.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+2473G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412568 | ||||||
chr2:100412854
|
A | C | 42 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(39): Show | 90 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.-33+2187T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412854 | ||||||
chr2:100412870
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-33+2171G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412870 | ||||||
chr2:100412982
|
C | A | 1 | a0001c0002t0001g0085 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-33+2059G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412982 | ||||||
chr2:100413449
|
G | A | 2 | a0001c0001t0005g0021a0001c0001t0005g0068 | 4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1592C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413449 | ||||||
chr2:100413543
|
C | A | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-33+1498G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413543 | ||||||
chr2:100413702
|
A | C | 1 | a0001c0002t0001g0087 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-33+1339T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413702 | ||||||
chr2:100413713
|
C | T | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+1328G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413713 | ||||||
chr2:100413810
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-33+1231A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413810 | ||||||
chr2:100413947
|
C | A | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+1094G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413947 | ||||||
chr2:100414019
|
C | T | 2 | a0001c0001t0005g0021a0001c0001t0005g0068 | 4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1022G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414019 | ||||||
chr2:100414130
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+911A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414130 | ||||||
chr2:100414282
|
C | A | 1 | a0005c0013t0028g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+759G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414282 | ||||||
chr2:100414286
|
C | T | 1 | a0001c0002t0001g0086 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-33+755G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414286 | ||||||
chr2:100414362
|
T | TCA | 14 | a0001c0001t0003g0005a0001c0001t0003g0023a0001c0001t0003g0024others(11): Show | 33 | HG01243.hp1 HG01891.hp1 HG02148.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33+677_-33+678dup others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414362 | ||||||
chr2:100414362
|
T | TCACA | 8 | a0001c0001t0005g0015a0001c0001t0005g0022a0001c0001t0005g0061others(5): Show | 14 | HG01167.hp2 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+675_-33+678dup others(4): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414362 | ||||||
chr2:100414362
|
T | TCACACA | 3 | a0001c0001t0005g0064a0001c0001t0005g0065a0005c0013t0028g0078 | 3 | HG03540.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+673_-33+678dup others(6): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414362 | ||||||
chr2:100414381
|
C | CAA | 3 | a0001c0001t0003g0007a0001c0007t0003g0017a0001c0007t0003g0073 | 14 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+658_-33+659dup others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414381 | ||||||
chr2:100414676
|
A | G | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-33+365T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414676 | ||||||
chr2:100414679
|
C | G | 1 | a0001c0001t0002g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-33+362G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414679 | ||||||
chr2:100414885
|
C | T | 7 | a0001c0002t0001g0060a0002c0005t0009g0031a0002c0005t0009g0059others(4): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+156G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414885 | ||||||
chr2:100414903
|
T | C | 1 | a0001c0003t0007g0079 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-33+138A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414903 | ||||||
chr2:100414988
|
A | T | 1 | a0001c0001t0002g0130 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-33+53T>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414988 | ||||||
chr2:100415112
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0122a0001c0002t0020g0053 | 5 | NA18972.hp2 NA18980.hp1 NA19003.hp1 others(2): Show |
splice_acceptor_variant&intron_variant | HIGH | c.-103-1G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415112 | ||||||
chr2:100415127
|
A | T | 1 | a0002c0005t0027g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-103-16T>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415127 | ||||||
chr2:100415278
|
T | G | 1 | a0001c0001t0002g0043 | 2 | NA18970.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-103-167A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415278 | ||||||
chr2:100415303
|
C | CA | 4 | a0001c0001t0005g0022a0001c0001t0005g0061a0001c0001t0005g0066others(1): Show | 6 | HG01167.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-193dupT | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415303 | ||||||
chr2:100415403
|
G | A | 50 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(47): Show | 113 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(110): Show |
intron_variant | MODIFIER | c.-103-292C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415403 | ||||||
chr2:100415628
|
A | G | 1 | a0001c0002t0001g0085 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-103-517T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415628 | ||||||
chr2:100415630
|
C | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0084 | 4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103-519G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415630 | ||||||
chr2:100415638
|
G | A | 1 | a0001c0001t0005g0068 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-103-527C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415638 | ||||||
chr2:100415757
|
C | T | 2 | a0001c0001t0012g0128a0001c0001t0012g0129 | 2 | HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-103-646G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415757 | ||||||
chr2:100415917
|
C | T | 4 | a0001c0001t0002g0020a0001c0001t0002g0043a0001c0001t0002g0123others(1): Show | 8 | HG00597.hp1 NA18945.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.-103-806G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415917 | ||||||
chr2:100415921
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-103-810G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415921 | ||||||
chr2:100416035
|
T | C | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-103-924A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416035 | ||||||
chr2:100416083
|
C | T | 1 | a0001c0001t0017g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-103-972G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416083 | ||||||
chr2:100416153
|
T | G | 1 | a0001c0001t0003g0074 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-103-1042A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416153 | ||||||
chr2:100416253
|
A | C | 24 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(21): Show | 60 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-104+1121T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416253 | ||||||
chr2:100416283
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(62): Show | 127 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-104+1091G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416283 | ||||||
chr2:100416354
|
A | G | 38 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0023others(35): Show | 84 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.-104+1020T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416354 | ||||||
chr2:100416467
|
T | C | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-104+907A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416467 | ||||||
chr2:100416688
|
A | AAAC | 14 | a0001c0001t0002g0123a0001c0001t0003g0005a0001c0001t0003g0007others(11): Show | 42 | HG00735.hp1 HG00741.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-104+683_-104+685d others(5): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416688 | ||||||
chr2:100416688
|
A | AAACAAC | 14 | a0001c0001t0005g0015a0001c0001t0005g0021a0001c0001t0005g0022others(11): Show | 22 | HG01167.hp2 HG01261.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-104+680_-104+685d others(8): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416688 | ||||||
chr2:100416688
|
A | AAACAACA others(2): Show |
7 | a0001c0001t0005g0061a0002c0005t0009g0031a0002c0005t0009g0059others(4): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104+677_-104+685d others(11): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416688 | ||||||
chr2:100417117
|
T | C | 1 | a0001c0002t0001g0122 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-104+257A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100417117 | ||||||
chr2:100417205
|
C | T | 7 | a0001c0002t0001g0060a0002c0005t0009g0031a0002c0005t0009g0059others(4): Show | 8 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104+169G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100417205 | ||||||
chr2:100417235
|
G | A | 59 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(56): Show | 119 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-104+139C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100417235 | ||||||
chr2:100417294
|
C | T | 165 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0020others(162): Show | 359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.-104+80G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100417294 |